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RRePSRéseau de Référence en Pathologie des Sarcomes des tissus mous et des viscèresSarcomes - GIST - Desmoïdes |
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RRePSRéseau de Référence en Pathologie des Sarcomes des tissus mous et des viscèresSarcomes - GIST - Desmoïdes |
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ID : 1070
Type : Constrained Content : TEXT Mandatory : Yes Multiple values : No Unique : No |
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Description : Centre RRePS
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Possible values :
Lyon CLB, LUMC, Reims CHU, Padova UNIPD, CHRU De Dijon, Nantes ICO , CHU Amiens, Milan INT, MEDIPATH Toulouse, Cy-Path, Mannheim, Lyon IHOP, Warsaw Cancer Center, Heidelberg, Hôp Pasteur, Hôp. Charles Nicolle, Hôp. Gabriel Montpied, Lausanne, Hôp. Pontchaillou, Labo. de Limoges, IHP Nantes, La Réunion CHU, KLEUVEN, Cabinet Mathurin, St Etienne ICLN-CHU, Cabinet de Douai, Cabinet de la Roquette, Cabinet de Reims, Reims IJG, Cabinet de Rennes, Cabinet d’Amiens, Bruxelles, Tenon, Bordeaux Pellegrin, Tübingen, Villejuif IGR, Service d'anapath de Brest, Centre Patho de Metz, Bicêtre, Centre Patho Dijon, Bonn, Saint-Louis, Bergonié, Curie, Nice CAL, Dijon CGFL, Caen CFB, Marseille IPC, Nancy ICL, Lille COL, Montpellier ICM, Angers ICO, IUCT Toulouse, Strasbourg CHU, CJP, Paris Henri Mondor, Timone, Cochin, Rennes CEM, Limoges Dupuytren, Tours Trousseau, Rouen CHB, Nantes CHU, Besançon CHU, Pitié Salpétrière, Haut-Lévèque Bordeaux, GHSN - LYON, Ambroise Paré APHP, CPS Strasbourg, Hôp. Civil Strasbourg, CHRU Caen, CHRU Brest, CHRU Montpellier, CHU Nancy, Rangueil Toulouse, Purpan Toulouse, CHRU Lille, CHRU Angers, Hôp. Nord Marseille, MEDIPATH, APHP Bichat, APHP Saint-Antoine, Lyon Edouard Herriot, CHR ORLEANS, Nice CHU, Cabinet Bièvres, OUEST PATHOLOGIE, CHU POITIERS, DIAG (Nice), GRP 2 RIVES, HPL, Centre François Baclesse Luxembourg |
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ID : 1031
Type : Free value Content : TEXT Mandatory : Yes Multiple values : No Unique : No |
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Description : Patient initials : 4 characters (2 of Lastname, 2 of Firstname)Attention to compound names
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ID : 140
Type : Free value Content : DATE Mandatory : Yes Multiple values : No Unique : No |
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Description : The patient's birth date
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ID : 141
Type : Constrained Content : TEXT Mandatory : Yes Multiple values : No Unique : No |
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Description : The patient's gender
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Possible values :
Female, Male |
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ID : 181
Type : Free value Content : DATE Mandatory : Yes Multiple values : No Unique : No |
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Description : The date when the patient has been created in the database
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ID : 1032
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Consent information
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Possible values :
Uninformed, Addressed mail, No opposition, Opposition, Consent |
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ID : 1
Type : Constrained Content : TEXT Mandatory : No Multiple values : Yes Unique : No |
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Description : No: no significant previous historyNF1: presence of neurofibromatosis type 1 or Recklinghausen diseaseNF2: presence of neurofibromatosis type 2Radiation therapy: tumour developed in a previously radiated areaLymphoedema: tumour developed on a preexisting lymphoedemaGardner: presence of a Gardner syndromLi Fraumeni: presence of a Li Fraumeni diseasePrevious cancer: the patient has previously developed another cancer different from the current tumourOther: other significant previous history with a possible link with the current tumour
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Possible values :
No, Previous cancer, NF1, NF2, Gardner syndrome, Li Fraumeni syndrome, Retinoblastoma syndrome, Immunodepressed - HIV, Immunodepressed - other, Ollier disease, Maffucci syndrome, Paget disease, Multiple osteochondromas, McCune-Albright syndrome, Rothmund-Thomson syndrome, Werner syndrome, Cherubism, Other genetic disease, Other, Unknown, Familial GISTs, Stratiakis-Carney dyad, Carney Triad, Other malignancy in family |
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ID : 1002
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Yes : tumour developed in a previously irradiated area
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Possible values :
No, Yes |
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ID : 1004
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Yes : tumour developed in a region with a preexisting lymphoedema
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Possible values :
No, Yes |
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ID : 1091
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : point de départ du développement de la tumeur |
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Possible values :
Soft tissue, Viscera, Bone |
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ID : 2
Type : Constrained Content : TEXT Mandatory : Yes Multiple values : No Unique : No |
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Description : Site of tumour according to the scroll menu
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Possible values :
- Soft tissue - Head and neck - Superficial areas of head - Sinus and nasal fossa - Deep facial areas - Orbit - Anterior skull base - Ear - lateral skull base and nasoharynx - Oral cavity - oropharynx - Larynx - trachea - Visceral space of the neck - Neck NOS - Other - Trunk wall - Chest wall - Axilla - Abdominal wall - Trunk - paraspinal - Buttock - Groin - Internal trunk - Retroperitoneum - Peritoneum - Pelvis - Thorax internal - Large vessels - Paratesticular - Lower limb - Thigh - Knee - Leg - Ankle - Foot - Toe - Upper limb - Shoulder girdle - Upper arm - Elbow - Forearm - Wrist - Hand - Finger - Viscera - Gastro Intestinal tractus - Oesophagus - Stomach - Duodenum - Appendix - Small intestine - Colon - Rectum - Anus - Gyneacological area - Uterus - Ovary - Fallopian tube - Vagina - Vulva - Others - Breast - Lung - Heart - Pleura - Thymus - Thyroid - Kidney - Bladder - Ureter - Prostate - Testis - Epididymis - Penis - Spleen - Liver - Pancreas - Gallbladder - Salivary gland - Tonsil - Adrenal - Brain - Meninges - Lymph node - Bone - Skull and face bone - Skull NOS - Ethmoid - Superior maxilla - Mandible - Bone face - Upper airways - Larynx - Bronchus - Nasal septum - Spine - Cervical spine - Dorsal spine - Lumbar spine - Basin, sacrum, coccyx - Basin - Sacrum - Coccyx - Hip joint - Other thoracic bone - Rib - Sternum - Clavicle - Superior limb and shoulder - Bone shoulder girdle - Scapula - Shoulder joint - Humerus - Elbow joint - Ulna - Radius - Wirst joint - Hand bone NOS - Carpal (Hand) - Metacarpals (Hand) - Hand phalanges - Hand joint - Inferior limb - Femur - Patella - Knee joint - Tibia - Fibula - Ankle joint - Bone foot NOS - Tarsals (Foot) - Metatarsals (Foot) - Foot phalanges - Foot joint |
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ID : 80
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
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Description : Largest diameter of the tumour expressed in mm
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ID : 3
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Superficial: the tumour is located above the superficial aponeurosis with no involvement of this aponeurosis Deep: the tumour is located beneath the superficial aponeurosis with no involvement of the area above this aponeurosis. Involvement of the aponeurosis is possibleSuperficial and deep: the tumour is located above and beneath the superficial aponeurosis
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Possible values :
Superficial, Superficial and deep, Deep, Surface, Cortical, Intra-medullary |
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ID : 1292
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Final diagnosis (computed)
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Possible values :
- Benign lesion - Benign adipocytic tumours - Angiolipoma - Angiomyolipoma - Chondroid lipoma - Hibernoma - Lipoblastoma/lipoblastomatosis - Lipoma - Lipomatosis - Lipomatosis of nerve - Myelolipoma - Atypical spindle cell/pleomorphic lipomatous tumour - Myolipoma - Spindle cell / pleomorphic lipoma - Benign chondrogenic tumours - Chondroblastoma NOS - Chondroma - Chondromyxoid fibroma - Enchondroma - Osteochondroma - Osteochondromyxoma - Periosteal chondroma - Pulmonary chondroma - Pulmonary hamartoma - Subungueal exostosis - Synovial chondromatosis - Benign fibroblastic/myofibroblastic tumours - Adenofibroma - Angiofibroma - Angiomyofibroblastoma - Calcifying aponeurotic fibroma - Calcifying fibrous tumour - Cellular angiofibroma - Desmoplastic fibroblastoma - Elastofibroma - Fasciitis - Fibroblastic tumour with SMAD3 fusion - Fibrochondromyxoid tumour with THBS1 fusion - Fibro-osseous pseudotumour of digits - Fibroma of tendon sheath - Fibromatosis colli - Fibrous hamartoma of infancy - Gardner fibroma - Inclusion body fibromatosis - Intra-nodal palisaded myofibroblastoma - Ischaemic fasciitis - Juvenile hyaline fibromatosis - Myofibroblastoma - Myositis ossificans - Nasopharyngeal angiofibroma - Nodular fasciitis - Nuchal-type fibroma - Organ-associated pseudosarcomatous myofibroblastic proliferations - Other fibromas - Proliferative fasciitis - Proliferative myositis - Benign fibro-histiocytic tumours - Central giant cell granuloma of jaws (giant cell reparative granuloma of jaws) - Deep benign fibrous histiocytoma - Epithelioid fibrous histiocytoma - Fibrous histiocytoma - Erdheim-Chester disease - Giant cell lesion of the small bones (extragnathic giant cell reparative granuloma) - Langerhans cell histiocytosis - Non Ossifying fibroma - Rosai-Dorfman disease - Tenosynovial giant cell tumour NOS - Tenosynovial giant cell tumour, diffuse type - Tenosynovial giant cell tumour, localized type - Benign nerve sheath tumours - Atypical neurofibromatous neoplasm of uncertain biological potential ANNUBP - Benign Triton tumour - Dermal nerve sheath myxoma - Ectopic meningioma - Granular cell tumour - Hybrid nerve sheath tumours - Nasal glial heterotopia - Neurofibroma - Neurothekeoma - Perineurioma - Plexiform neurofibroma - Schwannoma - Solitary circumscribed neuroma - Benign notochordal tumour - Benign osteogenic tumours - Osteoid osteoma - Osteoma - Benign pericytic tumours - Angioleiomyoma - Glomus tumour - Myofibroma / myofibromatosis - Myopericytoma - Benign skeletal muscle tumours - Rhabdomyoma - Rhabdomyoma - adult type - Rhabdomyoma - fetal type - Rhabdomyoma - genital type - Benign smooth muscle tumours - Adenomyoma - Atypical polypoid adenomyoma - Bizarre nuclei leiomyoma - Cellular leiomyoma - Diffuse leiomyomatosis - Dissecans leiomyoma - Epithelioid leiomyoma - Intraveinous leiomyomatosis - Leiomyoma - Leiomyomatosis peritonealis disseminata - Mitotically-active leiomyoma - Myxoid leiomyoma - Benign tumours of uncertain differentiation - Acral fibromyxoma - Brown tumour - Deep (aggressive) angiomyxoma - Ectopic hamartomatous thymoma - Fibrous dysplasia - Inflammatory fibroid polyp - Intramuscular myxoma - Myxoma NOS - Osteofibrous dysplasia - Pleomorphic hyalinizing angiectatic tumour - Pleuropulmonary blastoma - Simple bone cyst - Superficial angiomyxoma - Benign vascular tumours - Angiolymphoid hyperplasia - Angiomatosis - Atypical vascular lesion - Diffuse pulmonary lymphangiomatosis - Epithelioid hemangioma - Gorham disease - Hemangioma - Intra-muscular hemangioma - Lymphangiomatosis - Lymphangioma NOS - Pyogenic granuloma - Osseous pseudo-tumours - Bizarre parosteal osteochondromatous proliferation - Callus - Florid ossificans periostitis - Post-traumatic fibro-osseous lesion - Tophaceous pseudogout - Other benign lesion - GIST - gastrointestinal stromal tumour (GIST), low, very low risk - gastrointestinal stromal tumour (GIST), intermediate risk - gastrointestinal stromal tumour (GIST), high risk - Non-mesenchymal malignant tumour - Carcinoma - Germinal tumor - Lymphoma - Melanoma - Myeloma - Other non-mesenchymal malignant tumours - Plasmocytoma - Other diagnoses - Diagnosis unspecified - Undifferentiated malignant tumour - Sarcoma - Chondrosarcoma - Central chondrosarcoma - Chondrosarcoma, grade 1 - Chondrosarcoma, grade 2 - Chondrosarcoma, grade 3 - Chondrosarcoma NOS - Clear cell chondrosarcoma - Dedifferentiated chondrosarcoma - Mesenchymal chondrosarcoma - Periosteal chondrosarcoma - Peripheral chondrosarcoma - Leiomyosarcoma - Leiomyosarcoma - differentiated - Leiomyosarcoma - epithelioid - Leiomyosarcoma - myxoid - Leiomyosarcoma - poorly-differentiated - Liposarcoma - Liposarcoma - dedifferentiated - Liposarcoma - mixed type - Liposarcoma - myxoid - Liposarcoma - NOS - Liposarcoma - pleomorphic - Liposarcoma - round cell - Liposarcoma - well differentiated - Myxoid pleomorphic liposarcoma - Malignant fibrohistiocytic tumours of bone - Malignant giant cell tumour of bone - Malignant peripheral nerve sheath tumour - Ectomesenchymoma - Malignant perineurioma - Malignant Triton tumour - MPNST - epithelioid type - MPNST - usual type - Miscellaneous sarcomas - Fibrosarcoma NOS - Alveolar soft part sarcoma - Angiosarcoma - BCOR sarcoma - CIC-DUX sarcoma - CIC-rearranged sarcoma - Clear cell sarcoma - Desmoplastic round cell tumour - Epithelioid hemangioendothelioma NOS - Epithelioid hemangioendothelioma with TFE3 fusion - Epithelioid hemangioendothelioma with WWTR1 fusion - Epithelioid sarcoma - Ewing sarcoma - Extraskeletal myxoid chondrosarcoma - High risk solitary fibrous tumour - Intimal sarcoma - Low grade fibromyxoid sarcoma - Low grade sinonasal sarcoma - Malignant glomus tumour - Malignant granular cell tumour - Malignant mesenchymoma - Malignant mixed tumor - Malignant myoepithelial tumour - Malignant ossifying fibromyxoid tumour - Malignant PECOMA - Malignant rhabdoid tumour - Malignant tenosynovial giant cell tumour - Primary pulmonary myxoid sarcoma with EWSR1-CREB1 fusion - Sclerosing epithelioid fibrosarcoma - SMARCA4-deficient undifferentiated thoracic tumour - Myxofibrosarcoma - Osteosarcoma - Conventional osteosarcoma - Dedifferentiated low-grade central osteosarcoma - Dedifferentiated parosteal osteosarcoma - Extraskeletal osteosarcoma - High-grade surface osteosarcoma - Low-grade central osteosarcoma - Osteoblastoma-like osteosarcoma - Osteosarcoma NOS - Parosteal osteosarcoma - Periosteal osteosarcoma - Small cell osteosarcoma - Secondary osteosarcoma - Telangiectasic osteosarcoma - Other sarcomas - Adamantinoma - Adenosarcoma - Chondroid chordoma - Chordoma NOS - Dedifferentiated adamantimoma - Dedifferentiated chordoma - Endometrial stromal sarcoma - Endometrial stromal sarcoma - high-grade - Endometrial stromal sarcoma - low-grade - Phyllodes sarcoma - Poorly differenciated chordoma - Undifferentiated uterine sarcoma - Rhabdomyosarcoma - Adult spindle cell rhabdomyosarcoma - Alveolar rhabdomyosarcoma - Embryonal rhabdomyosarcoma - botryoid type - Embryonal rhabdomyosarcoma - NOS - Embryonal rhabdomyosarcoma - spindle cell type - Embryonal rhabdomyosarcoma - usual type - Pleomorphic rhabdomyosarcoma - Rhabdomyosarcoma - NOS - Rhabdomyosarcoma with MYOD1 mutation - Rhabdomyosarcoma with TFCP2 fusion - Rhabdomyosarcoma with VGLL2/NCOA2 fusion - Sclerosing rhabdomyosarcoma - Spindle cell rhabdomyosarcoma - Suspicion of sarcoma - Synovial sarcoma - Synovial sarcoma - biphasic - Synovial sarcoma - monophasic - Synovial sarcoma - NOS - Synovial sarcoma - poorly differentiated - Undifferentiated sarcoma - Undifferentiated epithelioid sarcoma - Undifferentiated pleomorphic sarcoma - Undifferentiated round cell sarcoma - Undifferentiated sarcoma - NOS - Undifferentiated spindle cell sarcoma - Tumour of intermediate malignancy - Atypical lipomatous tumour - Intermediate chondrogenic tumours - Atypical cartilaginous tumour - Cartilaginous tumour of uncertain prognosis - Chondromatosis NOS - Intermediate fibroblastic/myofibroblastic tumours - Dermatofibrosarcoma protuberans - Desmoid-type fibromatosis - Desmoplastic fibroma of bone - Fibro-osseous tumour of bone NOS - Fibrosarcomatous dermatofibrosarcoma protuberans - Giant cell fibroblastoma - Infantile fibrosarcoma - Inflammatory myofibroblastic tumour - Intermediate risk solitary fibrous tumour - Lipofibromatosis - Low grade myofibroblastic sarcoma - Low risk solitary fibrous tumour - Myxoinflammatory fibroblastic sarcoma - NTRK-rearranged spindle cell neoplasm - Palmar/plantar fibromatosis - Superficial CD34-positive fibroblastic tumour - Intermediate fibrohistiocytic tumours - Giant cell tumour of bone - Giant cell tumour of soft tissues - Metastatic giant cell tumour of bone - Osseous tumour rich in giant cell NOS - Plexiform fibrohistiocytic tumour - Suspicion of giant cell tumour of bone - Intermediate osteogenic tumours - Osteoblastoma NOS - Osteogenic tumor of uncertain prognosis (osteoblastoma versus osteoblastoma-like osteosarcoma) - Intermediate peripheral nerve sheath tumour - Malignant melanotic neural tumour - Intermediate tumours of uncertain differentiation - Aneurysmal bone cyst - Angiomatoid fibrous histiocytoma - Atypical fibroxanthoma - Cutaneous pleomorphic sarcoma - Hemosiderotic fibrolipomatous tumour - Lymphangioleiomyoma/lymphangioleiomyomatosis - Malignant phosphaturic mesenchymal tumour - Melanotic neuroectodermal tumour of infancy - Mesenchymal tumor with GLI1 alteration - Mixed tumour - Myoepithelioma - Ossifying fibromyxoid tumour - PECOMA - NOS - Phosphaturic mesenchymal tumour NOS - Intermediate vascular tumours - Composite hemangioendothelioma - Epithelioid vascular tumour of bone NOS - Kaposi sarcoma - Kaposiform hemangioendothelioma - Papillary intralymphatic angioendothelioma - Pseudomyogenic hemangioendothelioma - Retiform hemangioendothelioma - Other tumours of intermediate malignancy - Atypical smooth muscle tumour - EBV-associated smooth muscle tumour (STUMP) - Endometrial stromal nodule - Endometrial stromal tumor low-grade - Metastatic leiomyoma - Smooth muscle tumour of uncertain malignant potential (STUMP) - Smooth muscle tumour of undetermined malignant potential (STUMP) - Uterine tumour resembling ovarian sex cord tumours (UTROSCT) - Inflammatory rhabdomyoblastic tumour - Other intermediate mesenchymal tumour of bone - Mesenchymoma NOS - Osteofibrous dysplasia-like adamantinoma |
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ID : 1164
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
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Description :
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ID : 1033
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Origin of the sample
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Possible values :
Centre, Outside sampling, Systematic review, Second opinion |
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ID : 21
Type : Constrained Content : TEXT Mandatory : Yes Multiple values : No Unique : No |
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Description : Microbiopsy: sampling of the tumour with a core needleOpen biopsy: surgical resection of a piece of the tumour with a diagnostic intendTumour resection: surgical resection of the whole tumour
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Possible values :
Microbiopsy, Open biopsy, Tumour resection, Curettage |
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ID : 1048
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Monobloc: sample removed in one pieceFragmented: sample removed in several pieces
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Possible values :
Monobloc, Fragmented, Unknown |
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ID : 146
Type : Free value Content : DATE Mandatory : No Multiple values : No Unique : No |
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Description : Date on which the sample was removed
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ID : 1160
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
No, Yes |
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ID : 1161
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
No, Yes |
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ID : 1162
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
In progress, Negative, Non interpretable, Positive |
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ID : 1047
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Molecular Biology techniques performed
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Possible values :
No, Yes |
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ID : 1058
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
In progress, Negative, Positive, Non interpretable |
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ID : 1129
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
Not done, Done non interpretable, Done interpretable |
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ID : 1361
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Fusion transcript gene 1
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Possible values :
No transcrit, Other, A2M, ABHD12B, AC011523.2, ACBD5, ACSL3, ACSL5, ACTB, ACTN1, ADGRF5, AFAP1, AFF3, AGBL4, AGK, AGTRAP, AHCYL1, AHRR, AKAP13, AKAP9, AKT3, ALK, AMACR, AP3S1, APIP, ARHGAP12, ARID1A, ARID1B, ASPSCR1, ATF1, ATG16L1, ATIC, ATP11B, ATP2B4, ATXN1, AUTS2, BAG4, BAIAP2L1, BCAN, BCAP29, BCL10, BCL2, BCLAF1, BCOR, BCORL1, BCR, BICC1, BIRC3, BMX, BRAF, BRD1, BRD3, BRD4, BRD8, BTBD1, C11orf95, C19MC, C3orf62, C5orf30, CAB39L, CAD, CALML4, CAMTA1, CANT1, CAPZA2, CARMN, CARS, CASP7, CCAR2, CCDC6, CCDC67, CCDC88C, CCNB3, CCND1, CCNH, CD101, CD44, CD63, CD74, CD99L2, CDC27, CDH11, CDH17, CDK5RAP2, CDX1, CEACAM5, CEP128, CEP192, CEP89, CHCHD7, CHD7, CIC, CIITA, CITED1, CITED2, CLCN6, CLDN1, CLIP1, CLIP2, CLN6, CLTC, CNNM3, COL12A1, COL17A1, COL1A, COL1A1, COL1A2, COL3A1, COL6A3, COMMD10, CPG, CPSF6, CREB1, CREB3L1, CREB3L2, CREB3L3, CREBBP, CREBZF, CREM, CRTC1, CRTC3, CSF1, CTB.35F21.1, CTNNA3, CTNNB1, CXCR4, CXorf67, DACH1, DAXX, DCTN1, DDIT3, DDX3X, DDX5, DIP2C, DKKL1, DNAH5, DNAJB6, DST, DTD1, DUS4L, DUX4, DUX4L2, E2F1, EEF1AKMT3, EGF, EGFR, EHBP1, EIF3E, ELF5, ELK4, ELN, EMILIN2, EML4, EMP1, EP300, EP400, EPC1, EPC2, EPS15, ERBB2, ERC1, ERG, ERLIN2, ESR1, ESRP1, EST14, ETV1, ETV2, ETV4, ETV5, ETV6, EWSR1, EZR, FAM131B, FAM227A, FER, FEV, FGF1, FGF2, FGFR1, FGFR2, FGFR3, FHIT, FIP1L1, FLI1, FLJ60017, FN1, FOSB, FOXO1, FOXO4, FOXO6, FOXP1, FOXR1, FUS, GCC2, GCNT3, GIT2, GLI1, GNAI1, GOLGA5, GOLGB1, GOPC, GPN1, GPS2, GREB1, GRIK2, GRM1, GSN, GTF2I, GTF3C2, GUCA2B, HAS2, HBA, HBA2, HBB, HENMT1, HERV-K, HERVK17, HEY1, HIP1, HIPK1, HLA-A, HMGA1, HMGA2, HMGN2P46, HNRNPA2B1, HOOK1, HOOK3, HOXD13, HS6ST2, HSPA8, HTN3, HTT, IG, IGF2, IGFBP5, IGH, IGK, IGL, IKBKG, INO80D, IRF2BP2, IRF4/DUSP22, ITD, JAK2, JAZF1, KANSL1, KAT6B, KCTD7, KDM2A, KDM2B, KDM4B, KHDRB52, KHSRP, KIAA1217, KIAA1549, KIAA1598, KIF5B, KIFC3, KIRREL, KLC1, KLF15, KLF17, KLHL29, KLHL7, KLK2, KMT2A, KRAS, KTN1, LACTB2, LAMTOR1, LIFR, LMAN2L, LMNA, LPP, LRIG3, LRRC31, LRRC34, LRRC59, LRRFIP1, LRRFIP2, LSM14A, LUC7L3, LYN, MAD1L1, MAGI3, MALAT1, MALT1, MAML2, MAML3, MAN2A1, MAP3K8, MBD1, MBTD1, MDK, MEAF6, MECOM, MED12, MEF2C, MEIS1, MELK, MET, MGA, MIPOL1, MIR143HG, MITF, MKL2, MKRN1, MLL, MLL4, MLPH, MPRIP, MSANTD3, MSN, MTOR, MXD1, MYB, MYBL1, MYC, MYH10, MYH9, MYO5A, NAB2, NACC2, NAV2, NCOA1, NCOA2, NCOA3, NCOA4, NCOR2, ND4, NDRG1, NF1, NFASC, NFATC1, NFATC2, NFIA, NFIB, NOL4L, NONO, NOS2, NOTCH1, NOTCH2, NOTCH3, NPC1, NPM1, NR4A3, NRG1, NSD3, NTRK1, NTRK2, NTRK3, NUDCD3, NUMA1, NUP160, NUP214, NUP98, NUTM1, NUTM2A, NUTM2B, NUTM2E, OFD1, OGDH, OMD, PAFAH1B2, PAN3, PAPSS1, PARP14, PATZ1, PAX3, PAX5, PAX7, PAX8, PBX1, PBX3, PDCD1LG2, PDE3B, PDE4DIP, PDE8A, PDGFB, PDGFD, PDGFRA, PDGFRB, PDHX, PDPN, PHF1, PIK3C2A, PITPNC1, PLA2G6, PLAG1, PLIN3, PML, POM121, POU1F1, POU3F1, POU5F1, PPAPDC1A, PPARG, PPFIBP1, PPL, PPP1R1B, PPP6R3, PRB3, PRCC, PRDM10, PRG4, PRKAR1A, PRKCA, PRKCB, PRKCD, PRKD1, PRKDC, PRKG1, PSD2, PSMA8, PTCH1, PTEN, PTMA, PTPRD, PTPRJ, PTPRK, PTPRZ1, PVT1, PWWP2A, QKI, RAB2A, RABGAP1L, RAD51, RAD51B, RAD52, RAF1, RANBP2, RARG, RBM10, RCC1, RELA, RET, RFWD2, RNF13, RNF130, RNF213, ROS1, RP11.57H14.3, RPLP1, RPS11, RRBP1, RREB1, RSPO2, RSPO3, RUNX1, S100A10, SCARB1, SCYL3, SDC4, SEC31A, SEC61G, SERINC1, SERPINE1, SET, SETBP1, SFMBT1, SFPQ, SHH, SLC11A2, SLC12A7, SLC16A7, SLC1A2, SLC26A11, SLC34A2, SLC3A2, SLC43A3, SLC45A2, SLC45A3, SLC5A11, SLC7A14, SMAD2, SMAD3, SMARCA4, SMARCA5, SNAPC3, SND1, SNX19, SOS1, SOX6, SP3, SPATA16, SPECC1L, SPTBN1, SQSTM1, SRF, SS18, SS18L1, SSX1, SSX2, SSX2B, SSX4, STARD3, STAT6, STK32B, STRN, SUZ12, SVIL, TACC1, TACC3, TAF15, TAX1BP1, TBL1XR1, TCEA1, TCF12, TCF4, TCF7L2, TEAD1, TENM4, TERT, TFCP2, TFE3, TFEB, TFG, TGFBR3, THBS1, THRAP3, TIMP3, TLN2, TMEM135, TMPRSS2, TNC, TNS3, TOM1L2, TOP2B, TP53, TP53BP1, TPM1, TPM3, TPM4, TPR, TPRG1, TPTEP1, TRA2B, TRIM11, TRIM24, TRIM27, TRIM33, TRIM4, TRIO, TRIT1, TRMT11, TSFM, TTC17, TTC28, TTYH1, UBE2L3, UBR5, ULK4, USP6, VCL, VGLL2, VGLL3, VGLL4, VIM, VMP1, VTI1A, WDR91, WHSC1L1, WIF1, WT1, WWTR1, YAP1, YWHAE, YY1, ZC3H7B, ZCCHC8, ZFP36, ZFPM2, ZKSCAN1, ZKSCAN5, ZMYM2, ZNF207, ZNF217, ZNF278, ZNF423, ZNF444, ZNF521, ZNF595, ZNF737, ZNF9 |
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ID : 1360
Type : Free value Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Fusion transcript unlisted gene 1
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ID : 1362
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Fusion transcript gene 2
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Possible values :
No transcrit, Other, A2M, ABHD12B, AC011523.2, ACBD5, ACSL3, ACSL5, ACTB, ACTN1, ADGRF5, AFAP1, AFF3, AGBL4, AGK, AGTRAP, AHCYL1, AHRR, AKAP13, AKAP9, AKT3, ALK, AMACR, AP3S1, APIP, ARHGAP12, ARID1A, ARID1B, ASPSCR1, ATF1, ATG16L1, ATIC, ATP11B, ATP2B4, ATXN1, AUTS2, BAG4, BAIAP2L1, BCAN, BCAP29, BCL10, BCL2, BCLAF1, BCOR, BCORL1, BCR, BICC1, BIRC3, BMX, BRAF, BRD1, BRD3, BRD4, BRD8, BTBD1, C11orf95, C19MC, C3orf62, C5orf30, CAB39L, CAD, CALML4, CAMTA1, CANT1, CAPZA2, CARMN, CARS, CASP7, CCAR2, CCDC6, CCDC67, CCDC88C, CCNB3, CCND1, CCNH, CD101, CD44, CD63, CD74, CD99L2, CDC27, CDH11, CDH17, CDK5RAP2, CDX1, CEACAM5, CEP128, CEP192, CEP89, CHCHD7, CHD7, CIC, CIITA, CITED1, CITED2, CLCN6, CLDN1, CLIP1, CLIP2, CLN6, CLTC, CNNM3, COL12A1, COL17A1, COL1A, COL1A1, COL1A2, COL3A1, COL6A3, COMMD10, CPG, CPSF6, CREB1, CREB3L1, CREB3L2, CREB3L3, CREBBP, CREBZF, CREM, CRTC1, CRTC3, CSF1, CTB.35F21.1, CTNNA3, CTNNB1, CXCR4, CXorf67, DACH1, DAXX, DCTN1, DDIT3, DDX3X, DDX5, DIP2C, DKKL1, DNAH5, DNAJB6, DST, DTD1, DUS4L, DUX4, DUX4L2, E2F1, EEF1AKMT3, EGF, EGFR, EHBP1, EIF3E, ELF5, ELK4, ELN, EMILIN2, EML4, EMP1, EP300, EP400, EPC1, EPC2, EPS15, ERBB2, ERC1, ERG, ERLIN2, ESR1, ESRP1, EST14, ETV1, ETV2, ETV4, ETV5, ETV6, EWSR1, EZR, FAM131B, FAM227A, FER, FEV, FGF1, FGF2, FGFR1, FGFR2, FGFR3, FHIT, FIP1L1, FLI1, FLJ60017, FN1, FOSB, FOXO1, FOXO4, FOXO6, FOXP1, FOXR1, FUS, GCC2, GCNT3, GIT2, GLI1, GNAI1, GOLGA5, GOLGB1, GOPC, GPN1, GPS2, GREB1, GRIK2, GRM1, GSN, GTF2I, GTF3C2, GUCA2B, HAS2, HBA, HBA2, HBB, HENMT1, HERV-K, HERVK17, HEY1, HIP1, HIPK1, HLA-A, HMGA1, HMGA2, HMGN2P46, HNRNPA2B1, HOOK1, HOOK3, HOXD13, HS6ST2, HSPA8, HTN3, HTT, IG, IGF2, IGFBP5, IGH, IGK, IGL, IKBKG, INO80D, IRF2BP2, IRF4/DUSP22, ITD, JAK2, JAZF1, KANSL1, KAT6B, KCTD7, KDM2A, KDM2B, KDM4B, KHDRB52, KHSRP, KIAA1217, KIAA1549, KIAA1598, KIF5B, KIFC3, KIRREL, KLC1, KLF15, KLF17, KLHL29, KLHL7, KLK2, KMT2A, KRAS, KTN1, LACTB2, LAMTOR1, LIFR, LMAN2L, LMNA, LPP, LRIG3, LRRC31, LRRC34, LRRC59, LRRFIP1, LRRFIP2, LSM14A, LUC7L3, LYN, MAD1L1, MAGI3, MALAT1, MALT1, MAML2, MAML3, MAN2A1, MAP3K8, MBD1, MBTD1, MDK, MEAF6, MECOM, MED12, MEF2C, MEIS1, MELK, MET, MGA, MIPOL1, MIR143HG, MITF, MKL2, MKRN1, MLL, MLL4, MLPH, MPRIP, MSANTD3, MSN, MTOR, MXD1, MYB, MYBL1, MYC, MYH10, MYH9, MYO5A, NAB2, NACC2, NAV2, NCOA1, NCOA2, NCOA3, NCOA4, NCOR2, ND4, NDRG1, NF1, NFASC, NFATC1, NFATC2, NFIA, NFIB, NOL4L, NONO, NOS2, NOTCH1, NOTCH2, NOTCH3, NPC1, NPM1, NR4A3, NRG1, NSD3, NTRK1, NTRK2, NTRK3, NUDCD3, NUMA1, NUP160, NUP214, NUP98, NUTM1, NUTM2A, NUTM2B, NUTM2E, OFD1, OGDH, OMD, PAFAH1B2, PAN3, PAPSS1, PARP14, PATZ1, PAX3, PAX5, PAX7, PAX8, PBX1, PBX3, PDCD1LG2, PDE3B, PDE4DIP, PDE8A, PDGFB, PDGFD, PDGFRA, PDGFRB, PDHX, PDPN, PHF1, PIK3C2A, PITPNC1, PLA2G6, PLAG1, PLIN3, PML, POM121, POU1F1, POU3F1, POU5F1, PPAPDC1A, PPARG, PPFIBP1, PPL, PPP1R1B, PPP6R3, PRB3, PRCC, PRDM10, PRG4, PRKAR1A, PRKCA, PRKCB, PRKCD, PRKD1, PRKDC, PRKG1, PSD2, PSMA8, PTCH1, PTEN, PTMA, PTPRD, PTPRJ, PTPRK, PTPRZ1, PVT1, PWWP2A, QKI, RAB2A, RABGAP1L, RAD51, RAD51B, RAD52, RAF1, RANBP2, RARG, RBM10, RCC1, RELA, RET, RFWD2, RNF13, RNF130, RNF213, ROS1, RP11.57H14.3, RPLP1, RPS11, RRBP1, RREB1, RSPO2, RSPO3, RUNX1, S100A10, SCARB1, SCYL3, SDC4, SEC31A, SEC61G, SERINC1, SERPINE1, SET, SETBP1, SFMBT1, SFPQ, SHH, SLC11A2, SLC12A7, SLC16A7, SLC1A2, SLC26A11, SLC34A2, SLC3A2, SLC43A3, SLC45A2, SLC45A3, SLC5A11, SLC7A14, SMAD2, SMAD3, SMARCA4, SMARCA5, SNAPC3, SND1, SNX19, SOS1, SOX6, SP3, SPATA16, SPECC1L, SPTBN1, SQSTM1, SRF, SS18, SS18L1, SSX1, SSX2, SSX2B, SSX4, STARD3, STAT6, STK32B, STRN, SUZ12, SVIL, TACC1, TACC3, TAF15, TAX1BP1, TBL1XR1, TCEA1, TCF12, TCF4, TCF7L2, TEAD1, TENM4, TERT, TFCP2, TFE3, TFEB, TFG, TGFBR3, THBS1, THRAP3, TIMP3, TLN2, TMEM135, TMPRSS2, TNC, TNS3, TOM1L2, TOP2B, TP53, TP53BP1, TPM1, TPM3, TPM4, TPR, TPRG1, TPTEP1, TRA2B, TRIM11, TRIM24, TRIM27, TRIM33, TRIM4, TRIO, TRIT1, TRMT11, TSFM, TTC17, TTC28, TTYH1, UBE2L3, UBR5, ULK4, USP6, VCL, VGLL2, VGLL3, VGLL4, VIM, VMP1, VTI1A, WDR91, WHSC1L1, WIF1, WT1, WWTR1, YAP1, YWHAE, YY1, ZC3H7B, ZCCHC8, ZFP36, ZFPM2, ZKSCAN1, ZKSCAN5, ZMYM2, ZNF207, ZNF217, ZNF278, ZNF423, ZNF444, ZNF521, ZNF595, ZNF737, ZNF9 |
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ID : 1363
Type : Free value Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Fusion transcript unlisted gene 2
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ID : 1158
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
No, Yes |
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ID : 1159
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description :
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Possible values :
No, Yes |
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ID : 1163
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
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Description :
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ID : 999
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Initial pathologist
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ID : 1034
Type : Free value Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Sample reference in ACP structure
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ID : 1043
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Diagnosis made by the initial pathologist
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Possible values :
- Benign lesion - Benign adipocytic tumours - Angiolipoma - Angiomyolipoma - Chondroid lipoma - Hibernoma - Lipoblastoma/lipoblastomatosis - Lipoma - Lipomatosis - Lipomatosis of nerve - Atypical spindle cell/pleomorphic lipomatous tumour - Myelolipoma - Myolipoma - Spindle cell / pleomorphic lipoma - Benign chondrogenic tumours - Chondroma - Enchondroma - Osteochondroma - Chondroblastoma NOS - Chondromyxoid fibroma - Osteochondromyxoma - Periosteal chondroma - Pulmonary chondroma - Pulmonary hamartoma - Subungueal exostosis - Synovial chondromatosis - Benign fibroblastic/myofibroblastic tumours - Adenofibroma - Angiofibroma - Angiomyofibroblastoma - Calcifying aponeurotic fibroma - Calcifying fibrous tumour - Cellular angiofibroma - Desmoplastic fibroblastoma - Elastofibroma - Fasciitis - Fibroblastic tumour with SMAD3 fusion - Fibrochondromyxoid tumour with THBS1 fusion - Fibro-osseous pseudotumour of digits - Fibroma of tendon sheath - Fibromatosis colli - Fibrous hamartoma of infancy - Gardner fibroma - Inclusion body fibromatosis - Intra-nodal palisaded myofibroblastoma - Ischaemic fasciitis - Juvenile hyaline fibromatosis - Myofibroblastoma - Myositis ossificans - Nasopharyngeal angiofibroma - Nodular fasciitis - Nuchal-type fibroma - Organ-associated pseudosarcomatous myofibroblastic proliferations - Other fibromas - Proliferative fasciitis - Proliferative myositis - Benign fibro-histiocytic tumours - Central giant cell granuloma of jaws (giant cell reparative granuloma of jaws) - Deep benign fibrous histiocytoma - Epithelioid fibrous histiocytoma - Erdheim-Chester disease - Fibrous histiocytoma - Giant cell lesion of the small bones (extragnathic giant cell reparative granuloma) - Langerhans cell histiocytosis - Non Ossifying fibroma - Rosai-Dorfman disease - Tenosynovial giant cell tumour NOS - Tenosynovial giant cell tumour, diffuse type - Tenosynovial giant cell tumour, localized type - Benign nerve sheath tumours - Atypical neurofibromatous neoplasm of uncertain biological potential ANNUBP - Benign Triton tumour - Dermal nerve sheath myxoma - Ectopic meningioma - Granular cell tumour - Hybrid nerve sheath tumours - Nasal glial heterotopia - Neurofibroma - Neurothekeoma - Perineurioma - Plexiform neurofibroma - Schwannoma - Solitary circumscribed neuroma - Benign notochordal tumour - Benign osteogenic tumours - Osteoid osteoma - Osteoma - Benign pericytic tumours - Angioleiomyoma - Glomus tumour - Myofibroma / myofibromatosis - Myopericytoma - Benign skeletal muscle tumours - Rhabdomyoma - Rhabdomyoma - adult type - Rhabdomyoma - fetal type - Rhabdomyoma - genital type - Benign smooth muscle tumours - Adenomyoma - Atypical polypoid adenomyoma - Bizarre nuclei leiomyoma - Cellular leiomyoma - Diffuse leiomyomatosis - Dissecans leiomyoma - Epithelioid leiomyoma - Intraveinous leiomyomatosis - Leiomyoma - Leiomyomatosis peritonealis disseminata - Mitotically-active leiomyoma - Myxoid leiomyoma - Benign tumours of uncertain differentiation - Acral fibromyxoma - Brown tumour - Deep (aggressive) angiomyxoma - Ectopic hamartomatous thymoma - Fibrous dysplasia - Inflammatory fibroid polyp - Intramuscular myxoma - Myxoma NOS - Osteofibrous dysplasia - Pleomorphic hyalinizing angiectatic tumour - Pleuropulmonary blastoma - Simple bone cyst - Superficial angiomyxoma - Benign vascular tumours - Angiolymphoid hyperplasia - Angiomatosis - Atypical vascular lesion - Diffuse pulmonary lymphangiomatosis - Epithelioid hemangioma - Gorham disease - Hemangioma - Intra-muscular hemangioma - Lymphangioma NOS - Lymphangiomatosis - Pyogenic granuloma - Osseous pseudo-tumours - Bizarre parosteal osteochondromatous proliferation - Callus - Florid ossificans periostitis - Post-traumatic fibro-osseous lesion - Tophaceous pseudogout - Other benign lesion - GIST - gastrointestinal stromal tumour (GIST), low, very low risk - gastrointestinal stromal tumour (GIST), intermediate risk - gastrointestinal stromal tumour (GIST), high risk - Non-mesenchymal malignant tumour - Carcinoma - Germinal tumor - Lymphoma - Melanoma - Myeloma - Other non-mesenchymal malignant tumours - Plasmocytoma - Other diagnoses - Diagnosis unspecified - Undifferentiated malignant tumour - Sarcoma - Chondrosarcoma - Central chondrosarcoma - Chondrosarcoma, grade 1 - Chondrosarcoma, grade 2 - Chondrosarcoma, grade 3 - Chondrosarcoma NOS - Clear cell chondrosarcoma - Dedifferentiated chondrosarcoma - Mesenchymal chondrosarcoma - Periosteal chondrosarcoma - Peripheral chondrosarcoma - Leiomyosarcoma - Leiomyosarcoma - differentiated - Leiomyosarcoma - epithelioid - Leiomyosarcoma - myxoid - Leiomyosarcoma - poorly-differentiated - Liposarcoma - Liposarcoma - dedifferentiated - Liposarcoma - mixed type - Liposarcoma - myxoid - Liposarcoma - NOS - Liposarcoma - pleomorphic - Liposarcoma - round cell - Liposarcoma - well differentiated - Myxoid pleomorphic liposarcoma - Malignant fibrohistiocytic tumours of bone - Malignant giant cell tumour of bone - Malignant peripheral nerve sheath tumour - Ectomesenchymoma - Malignant perineurioma - Malignant Triton tumour - MPNST - epithelioid type - MPNST - usual type - Miscellaneous sarcomas - Alveolar soft part sarcoma - Angiosarcoma - BCOR sarcoma - CIC-DUX sarcoma - CIC-rearranged sarcoma - Clear cell sarcoma - Desmoplastic round cell tumour - Epithelioid hemangioendothelioma NOS - Epithelioid hemangioendothelioma with TFE3 fusion - Epithelioid hemangioendothelioma with WWTR1 fusion - Epithelioid sarcoma - Ewing sarcoma - Extraskeletal myxoid chondrosarcoma - Fibrosarcoma NOS - High risk solitary fibrous tumour - Intimal sarcoma - Low grade fibromyxoid sarcoma - Low grade sinonasal sarcoma - Malignant glomus tumour - Malignant granular cell tumour - Malignant mesenchymoma - Malignant mixed tumor - Malignant myoepithelial tumour - Malignant ossifying fibromyxoid tumour - Malignant PECOMA - Malignant rhabdoid tumour - Malignant tenosynovial giant cell tumour - Primary pulmonary myxoid sarcoma with EWSR1-CREB1 fusion - Sclerosing epithelioid fibrosarcoma - SMARCA4-deficient undifferentiated thoracic tumour - Myxofibrosarcoma - Osteosarcoma - Conventional osteosarcoma - Dedifferentiated low-grade central osteosarcoma - Dedifferentiated parosteal osteosarcoma - Extraskeletal osteosarcoma - High-grade surface osteosarcoma - Low-grade central osteosarcoma - Osteoblastoma-like osteosarcoma - Osteosarcoma NOS - Parosteal osteosarcoma - Periosteal osteosarcoma - Small cell osteosarcoma - Secondary osteosarcoma - Telangiectasic osteosarcoma - Other sarcomas - Adamantinoma - Adenosarcoma - Chondroid chordoma - Chordoma NOS - Dedifferentiated adamantimoma - Dedifferentiated chordoma - Endometrial stromal sarcoma - Endometrial stromal sarcoma - high-grade - Endometrial stromal sarcoma - low-grade - Phyllodes sarcoma - Poorly differenciated chordoma - Undifferentiated uterine sarcoma - Rhabdomyosarcoma - Adult spindle cell rhabdomyosarcoma - Alveolar rhabdomyosarcoma - Embryonal rhabdomyosarcoma - botryoid type - Embryonal rhabdomyosarcoma - NOS - Embryonal rhabdomyosarcoma - spindle cell type - Embryonal rhabdomyosarcoma - usual type - Pleomorphic rhabdomyosarcoma - Rhabdomyosarcoma - NOS - Sclerosing rhabdomyosarcoma - Spindle cell rhabdomyosarcoma - Rhabdomyosarcoma with VGLL2/NCOA2 fusion - Rhabdomyosarcoma with TFCP2 fusion - Rhabdomyosarcoma with MYOD1 mutation - Suspicion of sarcoma - Synovial sarcoma - Synovial sarcoma - biphasic - Synovial sarcoma - monophasic - Synovial sarcoma - NOS - Synovial sarcoma - poorly differentiated - Undifferentiated sarcoma - Undifferentiated epithelioid sarcoma - Undifferentiated pleomorphic sarcoma - Undifferentiated round cell sarcoma - Undifferentiated sarcoma - NOS - Undifferentiated spindle cell sarcoma - Tumour of intermediate malignancy - Atypical lipomatous tumour - Intermediate chondrogenic tumours - Atypical cartilaginous tumour - Cartilaginous tumour of uncertain prognosis - Chondromatosis NOS - Intermediate fibroblastic/myofibroblastic tumours - Dermatofibrosarcoma protuberans - Desmoid-type fibromatosis - Desmoplastic fibroma of bone - Fibro-osseous tumour of bone NOS - Fibrosarcomatous dermatofibrosarcoma protuberans - Giant cell fibroblastoma - Infantile fibrosarcoma - Inflammatory myofibroblastic tumour - Intermediate risk solitary fibrous tumour - Lipofibromatosis - Low grade myofibroblastic sarcoma - Low risk solitary fibrous tumour - Myxoinflammatory fibroblastic sarcoma - NTRK-rearranged spindle cell neoplasm - Palmar/plantar fibromatosis - Superficial CD34-positive fibroblastic tumour - Intermediate fibrohistiocytic tumours - Giant cell tumour of bone - Giant cell tumour of soft tissues - Metastatic giant cell tumour of bone - Osseous tumour rich in giant cell NOS - Plexiform fibrohistiocytic tumour - Suspicion of giant cell tumour of bone - Intermediate osteogenic tumours - Osteoblastoma NOS - Osteogenic tumor of uncertain prognosis (osteoblastoma versus osteoblastoma-like osteosarcoma) - Intermediate peripheral nerve sheath tumour - Malignant melanotic neural tumour - Intermediate tumours of uncertain differentiation - Aneurysmal bone cyst - Angiomatoid fibrous histiocytoma - Atypical fibroxanthoma - Cutaneous pleomorphic sarcoma - Hemosiderotic fibrolipomatous tumour - Lymphangioleiomyoma/lymphangioleiomyomatosis - Malignant phosphaturic mesenchymal tumour - Melanotic neuroectodermal tumour of infancy - Mesenchymal tumor with GLI1 alteration - Mixed tumour - Myoepithelioma - Ossifying fibromyxoid tumour - PECOMA - NOS - Phosphaturic mesenchymal tumour NOS - Intermediate vascular tumours - Composite hemangioendothelioma - Epithelioid vascular tumour of bone NOS - Kaposi sarcoma - Kaposiform hemangioendothelioma - Papillary intralymphatic angioendothelioma - Pseudomyogenic hemangioendothelioma - Retiform hemangioendothelioma - Other tumours of intermediate malignancy - Atypical smooth muscle tumour - EBV-associated smooth muscle tumour (STUMP) - Endometrial stromal nodule - Endometrial stromal tumor low-grade - Inflammatory rhabdomyoblastic tumour - Metastatic leiomyoma - Smooth muscle tumour of uncertain malignant potential (STUMP) - Smooth muscle tumour of undetermined malignant potential (STUMP) - Uterine tumour resembling ovarian sex cord tumours (UTROSCT) - Other intermediate mesenchymal tumour of bone - Osteofibrous dysplasia-like adamantinoma - Mesenchymoma NOS |
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ID : 1049
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : ACP grade
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Possible values :
1, 2, 3, Not applicable, Not done |
|
ID : 1052
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
|
Description : Mitotic count / 5mm² observed by the initial pathologist worked in the ACP structure
|
|
|
|
ID : 1067
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Initial pathologist observed if the tumour was spilt
|
|
Possible values :
Yes, No, Unknown |
|
ID : 1055
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : AFIP classification calculated by the initial pathologist
|
|
Possible values :
Very low risk, Low risk, Intermediate risk, High risk |
|
ID : 1165
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
|
Description :
|
|
|
|
ID : 1073
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Pathologist in the Regional Center who reviewed the sample
|
|
|
|
ID : 1035
Type : Free value Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Sample reference in the Regional Center
|
|
|
|
ID : 1037
Type : Free value Content : DATE Mandatory : No Multiple values : No Unique : No |
|
Description : When the sample was received in the Regional Center
|
|
|
|
ID : 1039
Type : Free value Content : DATE Mandatory : No Multiple values : No Unique : No |
|
Description : Date of diagnosis made by the pathologist in the Regional Center
|
|
|
|
ID : 1044
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Diagnosis made by the pathologist in the Regional Center
|
|
Possible values :
- Benign lesion - Benign adipocytic tumours - Angiolipoma - Angiomyolipoma - Chondroid lipoma - Hibernoma - Lipoblastoma/lipoblastomatosis - Lipoma - Lipomatosis - Lipomatosis of nerve - Atypical spindle cell/pleomorphic lipomatous tumour - Myelolipoma - Myolipoma - Spindle cell / pleomorphic lipoma - Benign chondrogenic tumours - Chondroblastoma NOS - Chondroma - Chondromyxoid fibroma - Enchondroma - Osteochondroma - Osteochondromyxoma - Periosteal chondroma - Pulmonary chondroma - Pulmonary hamartoma - Subungueal exostosis - Synovial chondromatosis - Benign fibroblastic/myofibroblastic tumours - Adenofibroma - Angiofibroma - Angiomyofibroblastoma - Calcifying aponeurotic fibroma - Calcifying fibrous tumour - Cellular angiofibroma - Desmoplastic fibroblastoma - Elastofibroma - Fasciitis - Fibroblastic tumour with SMAD3 fusion - Fibrochondromyxoid tumour with THBS1 fusion - Fibro-osseous pseudotumour of digits - Fibroma of tendon sheath - Fibromatosis colli - Fibrous hamartoma of infancy - Gardner fibroma - Inclusion body fibromatosis - Intra-nodal palisaded myofibroblastoma - Ischaemic fasciitis - Juvenile hyaline fibromatosis - Myofibroblastoma - Myositis ossificans - Nasopharyngeal angiofibroma - Nodular fasciitis - Nuchal-type fibroma - Organ-associated pseudosarcomatous myofibroblastic proliferations - Other fibromas - Proliferative fasciitis - Proliferative myositis - Benign fibro-histiocytic tumours - Central giant cell granuloma of jaws (giant cell reparative granuloma of jaws) - Deep benign fibrous histiocytoma - Epithelioid fibrous histiocytoma - Erdheim-Chester disease - Fibrous histiocytoma - Giant cell lesion of the small bones (extragnathic giant cell reparative granuloma) - Langerhans cell histiocytosis - Non Ossifying fibroma - Rosai-Dorfman disease - Tenosynovial giant cell tumour NOS - Tenosynovial giant cell tumour, diffuse type - Tenosynovial giant cell tumour, localized type - Benign nerve sheath tumours - Atypical neurofibromatous neoplasm of uncertain biological potential ANNUBP - Benign Triton tumour - Dermal nerve sheath myxoma - Ectopic meningioma - Granular cell tumour - Hybrid nerve sheath tumours - Nasal glial heterotopia - Neurofibroma - Neurothekeoma - Perineurioma - Plexiform neurofibroma - Schwannoma - Solitary circumscribed neuroma - Benign notochordal tumour - Benign osteogenic tumours - Osteoid osteoma - Osteoma - Benign pericytic tumours - Angioleiomyoma - Glomus tumour - Myofibroma / myofibromatosis - Myopericytoma - Benign skeletal muscle tumours - Rhabdomyoma - Rhabdomyoma - adult type - Rhabdomyoma - fetal type - Rhabdomyoma - genital type - Benign smooth muscle tumours - Adenomyoma - Atypical polypoid adenomyoma - Bizarre nuclei leiomyoma - Cellular leiomyoma - Diffuse leiomyomatosis - Dissecans leiomyoma - Epithelioid leiomyoma - Intraveinous leiomyomatosis - Leiomyoma - Leiomyomatosis peritonealis disseminata - Mitotically-active leiomyoma - Myxoid leiomyoma - Benign tumours of uncertain differentiation - Acral fibromyxoma - Brown tumour - Deep (aggressive) angiomyxoma - Ectopic hamartomatous thymoma - Fibrous dysplasia - Inflammatory fibroid polyp - Intramuscular myxoma - Myxoma NOS - Osteofibrous dysplasia - Pleomorphic hyalinizing angiectatic tumour - Pleuropulmonary blastoma - Simple bone cyst - Superficial angiomyxoma - Benign vascular tumours - Angiolymphoid hyperplasia - Angiomatosis - Atypical vascular lesion - Diffuse pulmonary lymphangiomatosis - Epithelioid hemangioma - Gorham disease - Hemangioma - Intra-muscular hemangioma - Lymphangioma NOS - Lymphangiomatosis - Pyogenic granuloma - Osseous pseudo-tumours - Bizarre parosteal osteochondromatous proliferation - Callus - Florid ossificans periostitis - Post-traumatic fibro-osseous lesion - Tophaceous pseudogout - Other benign lesion - GIST - gastrointestinal stromal tumour (GIST), low, very low risk - gastrointestinal stromal tumour (GIST), intermediate risk - gastrointestinal stromal tumour (GIST), high risk - Non-mesenchymal malignant tumour - Carcinoma - Germinal tumor - Lymphoma - Melanoma - Myeloma - Other non-mesenchymal malignant tumours - Plasmocytoma - Other diagnoses - Diagnosis unspecified - Undifferentiated malignant tumour - Sarcoma - Chondrosarcoma - Central chondrosarcoma - Chondrosarcoma, grade 1 - Chondrosarcoma, grade 2 - Chondrosarcoma, grade 3 - Chondrosarcoma NOS - Clear cell chondrosarcoma - Dedifferentiated chondrosarcoma - Mesenchymal chondrosarcoma - Periosteal chondrosarcoma - Peripheral chondrosarcoma - Leiomyosarcoma - Leiomyosarcoma - differentiated - Leiomyosarcoma - epithelioid - Leiomyosarcoma - myxoid - Leiomyosarcoma - poorly-differentiated - Liposarcoma - Liposarcoma - dedifferentiated - Liposarcoma - mixed type - Liposarcoma - myxoid - Liposarcoma - NOS - Liposarcoma - pleomorphic - Liposarcoma - round cell - Liposarcoma - well differentiated - Myxoid pleomorphic liposarcoma - Malignant fibrohistiocytic tumours of bone - Malignant giant cell tumour of bone - Malignant peripheral nerve sheath tumour - Ectomesenchymoma - Malignant perineurioma - Malignant Triton tumour - MPNST - epithelioid type - MPNST - usual type - Miscellaneous sarcomas - Alveolar soft part sarcoma - Angiosarcoma - BCOR sarcoma - CIC-DUX sarcoma - CIC-rearranged sarcoma - Clear cell sarcoma - Desmoplastic round cell tumour - Epithelioid hemangioendothelioma NOS - Epithelioid hemangioendothelioma with TFE3 fusion - Epithelioid hemangioendothelioma with WWTR1 fusion - Epithelioid sarcoma - Ewing sarcoma - Extraskeletal myxoid chondrosarcoma - Fibrosarcoma NOS - High risk solitary fibrous tumour - Intimal sarcoma - Low grade fibromyxoid sarcoma - Low grade sinonasal sarcoma - Malignant glomus tumour - Malignant granular cell tumour - Malignant mesenchymoma - Malignant mixed tumor - Malignant myoepithelial tumour - Malignant ossifying fibromyxoid tumour - Malignant PECOMA - Malignant rhabdoid tumour - Malignant tenosynovial giant cell tumour - Primary pulmonary myxoid sarcoma with EWSR1-CREB1 fusion - Sclerosing epithelioid fibrosarcoma - SMARCA4-deficient undifferentiated thoracic tumour - Myxofibrosarcoma - Osteosarcoma - Conventional osteosarcoma - Dedifferentiated low-grade central osteosarcoma - Dedifferentiated parosteal osteosarcoma - Extraskeletal osteosarcoma - High-grade surface osteosarcoma - Low-grade central osteosarcoma - Osteoblastoma-like osteosarcoma - Osteosarcoma NOS - Parosteal osteosarcoma - Periosteal osteosarcoma - Small cell osteosarcoma - Secondary osteosarcoma - Telangiectasic osteosarcoma - Other sarcomas - Adamantinoma - Adenosarcoma - Chondroid chordoma - Chordoma NOS - Dedifferentiated adamantimoma - Dedifferentiated chordoma - Endometrial stromal sarcoma - Endometrial stromal sarcoma - high-grade - Endometrial stromal sarcoma - low-grade - Phyllodes sarcoma - Undifferentiated uterine sarcoma - Poorly differenciated chordoma - Rhabdomyosarcoma - Adult spindle cell rhabdomyosarcoma - Alveolar rhabdomyosarcoma - Embryonal rhabdomyosarcoma - botryoid type - Embryonal rhabdomyosarcoma - NOS - Embryonal rhabdomyosarcoma - spindle cell type - Embryonal rhabdomyosarcoma - usual type - Pleomorphic rhabdomyosarcoma - Rhabdomyosarcoma - NOS - Rhabdomyosarcoma with MYOD1 mutation - Rhabdomyosarcoma with TFCP2 fusion - Rhabdomyosarcoma with VGLL2/NCOA2 fusion - Sclerosing rhabdomyosarcoma - Spindle cell rhabdomyosarcoma - Suspicion of sarcoma - Synovial sarcoma - Synovial sarcoma - biphasic - Synovial sarcoma - monophasic - Synovial sarcoma - NOS - Synovial sarcoma - poorly differentiated - Undifferentiated sarcoma - Undifferentiated epithelioid sarcoma - Undifferentiated pleomorphic sarcoma - Undifferentiated round cell sarcoma - Undifferentiated sarcoma - NOS - Undifferentiated spindle cell sarcoma - Tumour of intermediate malignancy - Atypical lipomatous tumour - Intermediate chondrogenic tumours - Atypical cartilaginous tumour - Cartilaginous tumour of uncertain prognosis - Chondromatosis NOS - Intermediate fibroblastic/myofibroblastic tumours - Dermatofibrosarcoma protuberans - Desmoid-type fibromatosis - Desmoplastic fibroma of bone - Fibro-osseous tumour of bone NOS - Fibrosarcomatous dermatofibrosarcoma protuberans - Giant cell fibroblastoma - Infantile fibrosarcoma - Inflammatory myofibroblastic tumour - Intermediate risk solitary fibrous tumour - Lipofibromatosis - Low grade myofibroblastic sarcoma - Low risk solitary fibrous tumour - Myxoinflammatory fibroblastic sarcoma - NTRK-rearranged spindle cell neoplasm - Palmar/plantar fibromatosis - Superficial CD34-positive fibroblastic tumour - Intermediate fibrohistiocytic tumours - Giant cell tumour of bone - Giant cell tumour of soft tissues - Metastatic giant cell tumour of bone - Osseous tumour rich in giant cell NOS - Plexiform fibrohistiocytic tumour - Suspicion of giant cell tumour of bone - Intermediate osteogenic tumours - Osteoblastoma NOS - Osteogenic tumor of uncertain prognosis (osteoblastoma versus osteoblastoma-like osteosarcoma) - Intermediate peripheral nerve sheath tumour - Malignant melanotic neural tumour - Intermediate tumours of uncertain differentiation - Aneurysmal bone cyst - Angiomatoid fibrous histiocytoma - Atypical fibroxanthoma - Cutaneous pleomorphic sarcoma - Hemosiderotic fibrolipomatous tumour - Lymphangioleiomyoma/lymphangioleiomyomatosis - Malignant phosphaturic mesenchymal tumour - Melanotic neuroectodermal tumour of infancy - Mesenchymal tumor with GLI1 alteration - Mixed tumour - Myoepithelioma - Ossifying fibromyxoid tumour - PECOMA - NOS - Phosphaturic mesenchymal tumour NOS - Intermediate vascular tumours - Composite hemangioendothelioma - Epithelioid vascular tumour of bone NOS - Kaposi sarcoma - Kaposiform hemangioendothelioma - Papillary intralymphatic angioendothelioma - Pseudomyogenic hemangioendothelioma - Retiform hemangioendothelioma - Other tumours of intermediate malignancy - Atypical smooth muscle tumour - EBV-associated smooth muscle tumour (STUMP) - Endometrial stromal nodule - Endometrial stromal tumor low-grade - Inflammatory rhabdomyoblastic tumour - Metastatic leiomyoma - Smooth muscle tumour of uncertain malignant potential (STUMP) - Smooth muscle tumour of undetermined malignant potential (STUMP) - Uterine tumour resembling ovarian sex cord tumours (UTROSCT) - Other intermediate mesenchymal tumour of bone - Mesenchymoma NOS - Osteofibrous dysplasia-like adamantinoma |
|
ID : 1050
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Tumour Grade observed by the expert pathologist in the Regional Center
|
|
Possible values :
1, 2, 3, Not applicable, Not done |
|
ID : 1053
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
|
Description : Mitotic count / 5mm² observed by the expert pathologist worked in the Regional Center
|
|
|
|
ID : 1068
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Regional Center pathologist observed if the tumour was spilt
|
|
Possible values :
Yes, No, Unknown |
|
ID : 1056
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : AFIP classification calculated in the Regional Center
|
|
Possible values :
Very low risk, Low risk, Intermediate risk, High risk |
|
ID : 1166
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
|
Description :
|
|
|
|
ID : 1074
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Pathologist in the National Center who reviewed the sample
|
|
|
|
ID : 1036
Type : Free value Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Sample reference in the National Center
|
|
|
|
ID : 1038
Type : Free value Content : DATE Mandatory : No Multiple values : No Unique : No |
|
Description : When the sample was received in the National Center
|
|
|
|
ID : 1040
Type : Free value Content : DATE Mandatory : No Multiple values : No Unique : No |
|
Description : Date of diagnosis made by the pathologist in the National Center
|
|
|
|
ID : 1045
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Diagnosis made by the pathologist in the National Center
|
|
Possible values :
- Benign lesion - Benign adipocytic tumours - Angiolipoma - Angiomyolipoma - Chondroid lipoma - Hibernoma - Lipoblastoma/lipoblastomatosis - Lipoma - Lipomatosis - Lipomatosis of nerve - Atypical spindle cell/pleomorphic lipomatous tumour - Myelolipoma - Myolipoma - Spindle cell / pleomorphic lipoma - Benign chondrogenic tumours - Chondroblastoma NOS - Chondroma - Chondromyxoid fibroma - Enchondroma - Osteochondroma - Osteochondromyxoma - Periosteal chondroma - Pulmonary chondroma - Pulmonary hamartoma - Subungueal exostosis - Synovial chondromatosis - Benign fibroblastic/myofibroblastic tumours - Adenofibroma - Angiofibroma - Angiomyofibroblastoma - Calcifying aponeurotic fibroma - Calcifying fibrous tumour - Cellular angiofibroma - Desmoplastic fibroblastoma - Elastofibroma - Fasciitis - Fibroblastic tumour with SMAD3 fusion - Fibrochondromyxoid tumour with THBS1 fusion - Fibro-osseous pseudotumour of digits - Fibroma of tendon sheath - Fibromatosis colli - Fibrous hamartoma of infancy - Gardner fibroma - Inclusion body fibromatosis - Intra-nodal palisaded myofibroblastoma - Ischaemic fasciitis - Juvenile hyaline fibromatosis - Myofibroblastoma - Myositis ossificans - Nasopharyngeal angiofibroma - Nodular fasciitis - Nuchal-type fibroma - Organ-associated pseudosarcomatous myofibroblastic proliferations - Other fibromas - Proliferative fasciitis - Proliferative myositis - Benign fibro-histiocytic tumours - Central giant cell granuloma of jaws (giant cell reparative granuloma of jaws) - Deep benign fibrous histiocytoma - Epithelioid fibrous histiocytoma - Erdheim-Chester disease - Fibrous histiocytoma - Giant cell lesion of the small bones (extragnathic giant cell reparative granuloma) - Langerhans cell histiocytosis - Non Ossifying fibroma - Rosai-Dorfman disease - Tenosynovial giant cell tumour NOS - Tenosynovial giant cell tumour, diffuse type - Tenosynovial giant cell tumour, localized type - Benign nerve sheath tumours - Atypical neurofibromatous neoplasm of uncertain biological potential ANNUBP - Benign Triton tumour - Dermal nerve sheath myxoma - Ectopic meningioma - Granular cell tumour - Hybrid nerve sheath tumours - Nasal glial heterotopia - Neurofibroma - Neurothekeoma - Perineurioma - Plexiform neurofibroma - Schwannoma - Solitary circumscribed neuroma - Benign notochordal tumour - Benign osteogenic tumours - Osteoid osteoma - Osteoma - Benign pericytic tumours - Angioleiomyoma - Glomus tumour - Myofibroma / myofibromatosis - Myopericytoma - Benign skeletal muscle tumours - Rhabdomyoma - Rhabdomyoma - adult type - Rhabdomyoma - fetal type - Rhabdomyoma - genital type - Benign smooth muscle tumours - Adenomyoma - Atypical polypoid adenomyoma - Bizarre nuclei leiomyoma - Cellular leiomyoma - Diffuse leiomyomatosis - Dissecans leiomyoma - Epithelioid leiomyoma - Intraveinous leiomyomatosis - Leiomyoma - Leiomyomatosis peritonealis disseminata - Mitotically-active leiomyoma - Myxoid leiomyoma - Benign tumours of uncertain differentiation - Acral fibromyxoma - Brown tumour - Deep (aggressive) angiomyxoma - Ectopic hamartomatous thymoma - Fibrous dysplasia - Inflammatory fibroid polyp - Intramuscular myxoma - Myxoma NOS - Osteofibrous dysplasia - Pleomorphic hyalinizing angiectatic tumour - Pleuropulmonary blastoma - Simple bone cyst - Superficial angiomyxoma - Benign vascular tumours - Angiolymphoid hyperplasia - Angiomatosis - Atypical vascular lesion - Diffuse pulmonary lymphangiomatosis - Epithelioid hemangioma - Gorham disease - Hemangioma - Intra-muscular hemangioma - Lymphangioma NOS - Lymphangiomatosis - Pyogenic granuloma - Osseous pseudo-tumours - Bizarre parosteal osteochondromatous proliferation - Callus - Florid ossificans periostitis - Post-traumatic fibro-osseous lesion - Tophaceous pseudogout - Other benign lesion - GIST - gastrointestinal stromal tumour (GIST), low, very low risk - gastrointestinal stromal tumour (GIST), intermediate risk - gastrointestinal stromal tumour (GIST), high risk - Non-mesenchymal malignant tumour - Carcinoma - Germinal tumor - Lymphoma - Melanoma - Myeloma - Other non-mesenchymal malignant tumours - Plasmocytoma - Other diagnoses - Undifferentiated malignant tumour - Diagnosis unspecified - Sarcoma - Chondrosarcoma - Central chondrosarcoma - Chondrosarcoma, grade 1 - Chondrosarcoma, grade 2 - Chondrosarcoma, grade 3 - Chondrosarcoma NOS - Clear cell chondrosarcoma - Dedifferentiated chondrosarcoma - Mesenchymal chondrosarcoma - Periosteal chondrosarcoma - Peripheral chondrosarcoma - Leiomyosarcoma - Leiomyosarcoma - differentiated - Leiomyosarcoma - epithelioid - Leiomyosarcoma - myxoid - Leiomyosarcoma - poorly-differentiated - Liposarcoma - Liposarcoma - dedifferentiated - Liposarcoma - mixed type - Liposarcoma - myxoid - Liposarcoma - NOS - Liposarcoma - pleomorphic - Liposarcoma - round cell - Liposarcoma - well differentiated - Myxoid pleomorphic liposarcoma - Malignant fibrohistiocytic tumours of bone - Malignant giant cell tumour of bone - Malignant peripheral nerve sheath tumour - Ectomesenchymoma - Malignant perineurioma - Malignant Triton tumour - MPNST - epithelioid type - MPNST - usual type - Miscellaneous sarcomas - Fibrosarcoma NOS - Alveolar soft part sarcoma - Angiosarcoma - BCOR sarcoma - CIC-DUX sarcoma - CIC-rearranged sarcoma - Clear cell sarcoma - Desmoplastic round cell tumour - Epithelioid hemangioendothelioma NOS - Epithelioid hemangioendothelioma with TFE3 fusion - Epithelioid hemangioendothelioma with WWTR1 fusion - Epithelioid sarcoma - Ewing sarcoma - Extraskeletal myxoid chondrosarcoma - High risk solitary fibrous tumour - Intimal sarcoma - Low grade fibromyxoid sarcoma - Low grade sinonasal sarcoma - Malignant glomus tumour - Malignant granular cell tumour - Malignant mesenchymoma - Malignant mixed tumor - Malignant myoepithelial tumour - Malignant ossifying fibromyxoid tumour - Malignant PECOMA - Malignant rhabdoid tumour - Malignant tenosynovial giant cell tumour - Primary pulmonary myxoid sarcoma with EWSR1-CREB1 fusion - Sclerosing epithelioid fibrosarcoma - SMARCA4-deficient undifferentiated thoracic tumour - Myxofibrosarcoma - Osteosarcoma - Conventional osteosarcoma - Dedifferentiated low-grade central osteosarcoma - Dedifferentiated parosteal osteosarcoma - Extraskeletal osteosarcoma - High-grade surface osteosarcoma - Low-grade central osteosarcoma - Osteoblastoma-like osteosarcoma - Osteosarcoma NOS - Parosteal osteosarcoma - Periosteal osteosarcoma - Small cell osteosarcoma - Secondary osteosarcoma - Telangiectasic osteosarcoma - Other sarcomas - Adamantinoma - Adenosarcoma - Chondroid chordoma - Chordoma NOS - Dedifferentiated adamantimoma - Dedifferentiated chordoma - Endometrial stromal sarcoma - Endometrial stromal sarcoma - high-grade - Endometrial stromal sarcoma - low-grade - Phyllodes sarcoma - Poorly differenciated chordoma - Undifferentiated uterine sarcoma - Rhabdomyosarcoma - Adult spindle cell rhabdomyosarcoma - Alveolar rhabdomyosarcoma - Embryonal rhabdomyosarcoma - botryoid type - Embryonal rhabdomyosarcoma - NOS - Embryonal rhabdomyosarcoma - spindle cell type - Embryonal rhabdomyosarcoma - usual type - Pleomorphic rhabdomyosarcoma - Rhabdomyosarcoma - NOS - Rhabdomyosarcoma with MYOD1 mutation - Rhabdomyosarcoma with TFCP2 fusion - Rhabdomyosarcoma with VGLL2/NCOA2 fusion - Sclerosing rhabdomyosarcoma - Spindle cell rhabdomyosarcoma - Suspicion of sarcoma - Synovial sarcoma - Synovial sarcoma - biphasic - Synovial sarcoma - monophasic - Synovial sarcoma - NOS - Synovial sarcoma - poorly differentiated - Undifferentiated sarcoma - Undifferentiated epithelioid sarcoma - Undifferentiated pleomorphic sarcoma - Undifferentiated round cell sarcoma - Undifferentiated sarcoma - NOS - Undifferentiated spindle cell sarcoma - Tumour of intermediate malignancy - Atypical lipomatous tumour - Giant cell tumour of bone - Intermediate chondrogenic tumours - Atypical cartilaginous tumour - Cartilaginous tumour of uncertain prognosis - Chondromatosis NOS - Intermediate fibroblastic/myofibroblastic tumours - Dermatofibrosarcoma protuberans - Desmoid-type fibromatosis - Desmoplastic fibroma of bone - Fibro-osseous tumour of bone NOS - Fibrosarcomatous dermatofibrosarcoma protuberans - Giant cell fibroblastoma - Infantile fibrosarcoma - Inflammatory myofibroblastic tumour - Intermediate risk solitary fibrous tumour - Lipofibromatosis - Low grade myofibroblastic sarcoma - Low risk solitary fibrous tumour - Myxoinflammatory fibroblastic sarcoma - NTRK-rearranged spindle cell neoplasm - Palmar/plantar fibromatosis - Superficial CD34-positive fibroblastic tumour - Intermediate fibrohistiocytic tumours - Giant cell tumour of soft tissues - Metastatic giant cell tumour of bone - Osseous tumour rich in giant cell NOS - Plexiform fibrohistiocytic tumour - Suspicion of giant cell tumour of bone - Intermediate osteogenic tumours - Osteoblastoma NOS - Osteogenic tumor of uncertain prognosis (osteoblastoma versus osteoblastoma-like osteosarcoma) - Intermediate peripheral nerve sheath tumour - Malignant melanotic neural tumour - Intermediate tumours of uncertain differentiation - Aneurysmal bone cyst - Angiomatoid fibrous histiocytoma - Atypical fibroxanthoma - Cutaneous pleomorphic sarcoma - Hemosiderotic fibrolipomatous tumour - Lymphangioleiomyoma/lymphangioleiomyomatosis - Malignant phosphaturic mesenchymal tumour - Melanotic neuroectodermal tumour of infancy - Mesenchymal tumor with GLI1 alteration - Mixed tumour - Myoepithelioma - Ossifying fibromyxoid tumour - PECOMA - NOS - Phosphaturic mesenchymal tumour NOS - Intermediate vascular tumours - Composite hemangioendothelioma - Epithelioid vascular tumour of bone NOS - Kaposi sarcoma - Kaposiform hemangioendothelioma - Papillary intralymphatic angioendothelioma - Pseudomyogenic hemangioendothelioma - Retiform hemangioendothelioma - Other tumours of intermediate malignancy - Atypical smooth muscle tumour - EBV-associated smooth muscle tumour (STUMP) - Endometrial stromal nodule - Endometrial stromal tumor low-grade - Inflammatory rhabdomyoblastic tumour - Metastatic leiomyoma - Smooth muscle tumour of uncertain malignant potential (STUMP) - Smooth muscle tumour of undetermined malignant potential (STUMP) - Uterine tumour resembling ovarian sex cord tumours (UTROSCT) - Other intermediate mesenchymal tumour of bone - Mesenchymoma NOS - Osteofibrous dysplasia-like adamantinoma |
|
ID : 1051
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Tumour Grade observed by the expert pathologist in the National Center
|
|
Possible values :
1, 2, 3, Not applicable, Not done |
|
ID : 1054
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
|
Description : Mitotic count / 5mm² observed by the expert pathologist worked in the National Center
|
|
|
|
ID : 1069
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : National Center pathologist observed if the tumour was spilt
|
|
Possible values :
Yes, No, Unknown |
|
ID : 1057
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : AFIP classification calculated in the National Center
|
|
Possible values :
Very low risk, Low risk, Intermediate risk, High risk |
|
ID : 1041
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Sample reviewed by several experts pathologists during the national reviewing
|
|
Possible values :
No, Yes |
|
ID : 1059
Type : Free value Content : DATE Mandatory : No Multiple values : No Unique : No |
|
Description : Date of the national reviewing
|
|
|
|
ID : 1064
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : The pathologist name who presented the sample
|
|
Possible values :
- Coordinator site - TOURS Trousseau - CLB - Institut Bergonié - IGR - Reference Center - ANGERS - BORDEAUX - LILLE - LYON - MARSEILLE - NANCY - NANTES - PARIS Cochin - PARIS centre Huguenin - STRASBOURG - TOULOUSE - TOURS - Contributing center - CAEN - PARIS Trousseau - RENNES - ROUEN |
|
ID : 1060
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
|
Description : Diagnosis reviewed by several experts pathologists during the national reviewing
|
|
Possible values :
- Benign lesion - Benign adipocytic tumours - Angiolipoma - Angiomyolipoma - Chondroid lipoma - Hibernoma - Lipoblastoma/lipoblastomatosis - Lipoma - Lipomatosis - Lipomatosis of nerve - Myelolipoma - Atypical spindle cell/pleomorphic lipomatous tumour - Myolipoma - Spindle cell / pleomorphic lipoma - Benign chondrogenic tumours - Chondroblastoma NOS - Chondroma - Chondromyxoid fibroma - Enchondroma - Osteochondroma - Osteochondromyxoma - Periosteal chondroma - Pulmonary chondroma - Pulmonary hamartoma - Subungueal exostosis - Synovial chondromatosis - Benign fibroblastic/myofibroblastic tumours - Adenofibroma - Angiofibroma - Angiomyofibroblastoma - Calcifying aponeurotic fibroma - Calcifying fibrous tumour - Cellular angiofibroma - Desmoplastic fibroblastoma - Elastofibroma - Fasciitis - Fibroblastic tumour with SMAD3 fusion - Fibrochondromyxoid tumour with THBS1 fusion - Fibro-osseous pseudotumour of digits - Fibroma of tendon sheath - Fibromatosis colli - Fibrous hamartoma of infancy - Gardner fibroma - Inclusion body fibromatosis - Intra-nodal palisaded myofibroblastoma - Ischaemic fasciitis - Juvenile hyaline fibromatosis - Myofibroblastoma - Myositis ossificans - Nasopharyngeal angiofibroma - Nodular fasciitis - Nuchal-type fibroma - Organ-associated pseudosarcomatous myofibroblastic proliferations - Other fibromas - Proliferative fasciitis - Proliferative myositis - Benign fibro-histiocytic tumours - Central giant cell granuloma of jaws (giant cell reparative granuloma of jaws) - Deep benign fibrous histiocytoma - Epithelioid fibrous histiocytoma - Erdheim-Chester disease - Fibrous histiocytoma - Giant cell lesion of the small bones (extragnathic giant cell reparative granuloma) - Langerhans cell histiocytosis - Non Ossifying fibroma - Rosai-Dorfman disease - Tenosynovial giant cell tumour NOS - Tenosynovial giant cell tumour, diffuse type - Tenosynovial giant cell tumour, localized type - Benign nerve sheath tumours - Atypical neurofibromatous neoplasm of uncertain biological potential ANNUBP - Benign Triton tumour - Dermal nerve sheath myxoma - Ectopic meningioma - Granular cell tumour - Hybrid nerve sheath tumours - Nasal glial heterotopia - Neurofibroma - Neurothekeoma - Perineurioma - Plexiform neurofibroma - Schwannoma - Solitary circumscribed neuroma - Benign notochordal tumour - Benign osteogenic tumours - Osteoid osteoma - Osteoma - Benign pericytic tumours - Angioleiomyoma - Glomus tumour - Myofibroma / myofibromatosis - Myopericytoma - Benign skeletal muscle tumours - Rhabdomyoma - Rhabdomyoma - adult type - Rhabdomyoma - fetal type - Rhabdomyoma - genital type - Benign smooth muscle tumours - Adenomyoma - Atypical polypoid adenomyoma - Bizarre nuclei leiomyoma - Cellular leiomyoma - Diffuse leiomyomatosis - Dissecans leiomyoma - Epithelioid leiomyoma - Intraveinous leiomyomatosis - Leiomyoma - Leiomyomatosis peritonealis disseminata - Mitotically-active leiomyoma - Myxoid leiomyoma - Benign tumours of uncertain differentiation - Acral fibromyxoma - Brown tumour - Deep (aggressive) angiomyxoma - Ectopic hamartomatous thymoma - Fibrous dysplasia - Inflammatory fibroid polyp - Intramuscular myxoma - Myxoma NOS - Osteofibrous dysplasia - Pleomorphic hyalinizing angiectatic tumour - Pleuropulmonary blastoma - Simple bone cyst - Superficial angiomyxoma - Benign vascular tumours - Angiolymphoid hyperplasia - Angiomatosis - Atypical vascular lesion - Diffuse pulmonary lymphangiomatosis - Epithelioid hemangioma - Gorham disease - Hemangioma - Intra-muscular hemangioma - Lymphangioma NOS - Lymphangiomatosis - Pyogenic granuloma - Osseous pseudo-tumours - Bizarre parosteal osteochondromatous proliferation - Callus - Florid ossificans periostitis - Post-traumatic fibro-osseous lesion - Tophaceous pseudogout - Other benign lesion - GIST - gastrointestinal stromal tumour (GIST), low, very low risk - gastrointestinal stromal tumour (GIST), intermediate risk - gastrointestinal stromal tumour (GIST), high risk - Non-mesenchymal malignant tumour - Carcinoma - Germinal tumor - Lymphoma - Melanoma - Myeloma - Other non-mesenchymal malignant tumours - Plasmocytoma - Other diagnoses - Diagnosis unspecified - Undifferentiated malignant tumour - Sarcoma - Chondrosarcoma - Central chondrosarcoma - Chondrosarcoma, grade 1 - Chondrosarcoma, grade 2 - Chondrosarcoma, grade 3 - Chondrosarcoma NOS - Clear cell chondrosarcoma - Dedifferentiated chondrosarcoma - Mesenchymal chondrosarcoma - Periosteal chondrosarcoma - Peripheral chondrosarcoma - Leiomyosarcoma - Leiomyosarcoma - differentiated - Leiomyosarcoma - epithelioid - Leiomyosarcoma - myxoid - Leiomyosarcoma - poorly-differentiated - Liposarcoma - Liposarcoma - dedifferentiated - Liposarcoma - mixed type - Liposarcoma - myxoid - Liposarcoma - NOS - Liposarcoma - pleomorphic - Liposarcoma - round cell - Liposarcoma - well differentiated - Myxoid pleomorphic liposarcoma - Malignant fibrohistiocytic tumours of bone - Malignant giant cell tumour of bone - Malignant peripheral nerve sheath tumour - Ectomesenchymoma - Malignant perineurioma - Malignant Triton tumour - MPNST - epithelioid type - MPNST - usual type - Miscellaneous sarcomas - Alveolar soft part sarcoma - Angiosarcoma - BCOR sarcoma - CIC-DUX sarcoma - CIC-rearranged sarcoma - Clear cell sarcoma - Desmoplastic round cell tumour - Epithelioid hemangioendothelioma NOS - Epithelioid hemangioendothelioma with TFE3 fusion - Epithelioid hemangioendothelioma with WWTR1 fusion - Epithelioid sarcoma - Ewing sarcoma - Extraskeletal myxoid chondrosarcoma - Fibrosarcoma NOS - High risk solitary fibrous tumour - Intimal sarcoma - Low grade fibromyxoid sarcoma - Low grade sinonasal sarcoma - Malignant glomus tumour - Malignant granular cell tumour - Malignant mesenchymoma - Malignant mixed tumor - Malignant myoepithelial tumour - Malignant ossifying fibromyxoid tumour - Malignant PECOMA - Malignant rhabdoid tumour - Malignant tenosynovial giant cell tumour - Primary pulmonary myxoid sarcoma with EWSR1-CREB1 fusion - Sclerosing epithelioid fibrosarcoma - SMARCA4-deficient undifferentiated thoracic tumour - Myxofibrosarcoma - Osteosarcoma - Conventional osteosarcoma - Dedifferentiated low-grade central osteosarcoma - Dedifferentiated parosteal osteosarcoma - Extraskeletal osteosarcoma - High-grade surface osteosarcoma - Low-grade central osteosarcoma - Osteoblastoma-like osteosarcoma - Osteosarcoma NOS - Parosteal osteosarcoma - Periosteal osteosarcoma - Small cell osteosarcoma - Secondary osteosarcoma - Telangiectasic osteosarcoma - Other sarcomas - Adamantinoma - Adenosarcoma - Chondroid chordoma - Chordoma NOS - Dedifferentiated adamantimoma - Dedifferentiated chordoma - Endometrial stromal sarcoma - Endometrial stromal sarcoma - high-grade - Endometrial stromal sarcoma - low-grade - Phyllodes sarcoma - Poorly differenciated chordoma - Undifferentiated uterine sarcoma - Rhabdomyosarcoma - Adult spindle cell rhabdomyosarcoma - Alveolar rhabdomyosarcoma - Embryonal rhabdomyosarcoma - botryoid type - Embryonal rhabdomyosarcoma - NOS - Embryonal rhabdomyosarcoma - spindle cell type - Embryonal rhabdomyosarcoma - usual type - Pleomorphic rhabdomyosarcoma - Rhabdomyosarcoma - NOS - Rhabdomyosarcoma with MYOD1 mutation - Rhabdomyosarcoma with TFCP2 fusion - Rhabdomyosarcoma with VGLL2/NCOA2 fusion - Sclerosing rhabdomyosarcoma - Spindle cell rhabdomyosarcoma - Suspicion of sarcoma - Synovial sarcoma - Synovial sarcoma - biphasic - Synovial sarcoma - monophasic - Synovial sarcoma - NOS - Synovial sarcoma - poorly differentiated - Undifferentiated sarcoma - Undifferentiated epithelioid sarcoma - Undifferentiated pleomorphic sarcoma - Undifferentiated round cell sarcoma - Undifferentiated sarcoma - NOS - Undifferentiated spindle cell sarcoma - Tumour of intermediate malignancy - Atypical lipomatous tumour - Intermediate chondrogenic tumours - Atypical cartilaginous tumour - Cartilaginous tumour of uncertain prognosis - Chondromatosis NOS - Intermediate fibroblastic/myofibroblastic tumours - Dermatofibrosarcoma protuberans - Desmoid-type fibromatosis - Desmoplastic fibroma of bone - Fibro-osseous tumour of bone NOS - Fibrosarcomatous dermatofibrosarcoma protuberans - Giant cell fibroblastoma - Infantile fibrosarcoma - Inflammatory myofibroblastic tumour - Intermediate risk solitary fibrous tumour - Lipofibromatosis - Low grade myofibroblastic sarcoma - Low risk solitary fibrous tumour - Myxoinflammatory fibroblastic sarcoma - NTRK-rearranged spindle cell neoplasm - Palmar/plantar fibromatosis - Superficial CD34-positive fibroblastic tumour - Intermediate fibrohistiocytic tumours - Giant cell tumour of soft tissues - Giant cell tumour of bone - Metastatic giant cell tumour of bone - Osseous tumour rich in giant cell NOS - Plexiform fibrohistiocytic tumour - Suspicion of giant cell tumour of bone - Intermediate osteogenic tumours - Osteoblastoma NOS - Osteogenic tumor of uncertain prognosis (osteoblastoma versus osteoblastoma-like osteosarcoma) - Intermediate peripheral nerve sheath tumour - Malignant melanotic neural tumour - Intermediate tumours of uncertain differentiation - Aneurysmal bone cyst - Angiomatoid fibrous histiocytoma - Atypical fibroxanthoma - Cutaneous pleomorphic sarcoma - Hemosiderotic fibrolipomatous tumour - Lymphangioleiomyoma/lymphangioleiomyomatosis - Malignant phosphaturic mesenchymal tumour - Melanotic neuroectodermal tumour of infancy - Mesenchymal tumor with GLI1 alteration - Mixed tumour - Myoepithelioma - Ossifying fibromyxoid tumour - PECOMA - NOS - Phosphaturic mesenchymal tumour NOS - Intermediate vascular tumours - Composite hemangioendothelioma - Epithelioid vascular tumour of bone NOS - Kaposi sarcoma - Kaposiform hemangioendothelioma - Papillary intralymphatic angioendothelioma - Pseudomyogenic hemangioendothelioma - Retiform hemangioendothelioma - Other tumours of intermediate malignancy - Atypical smooth muscle tumour - EBV-associated smooth muscle tumour (STUMP) - Endometrial stromal nodule - Endometrial stromal tumor low-grade - Inflammatory rhabdomyoblastic tumour - Metastatic leiomyoma - Smooth muscle tumour of uncertain malignant potential (STUMP) - Smooth muscle tumour of undetermined malignant potential (STUMP) - Uterine tumour resembling ovarian sex cord tumours (UTROSCT) - Other intermediate mesenchymal tumour of bone - Mesenchymoma NOS - Osteofibrous dysplasia-like adamantinoma |
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ID : 1062
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Grade reviewed by several experts pathologists during the national reviewing
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Possible values :
1, 2, 3, Not applicable, Not done |
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ID : 1063
Type : Free value Content : INTEGER Mandatory : No Multiple values : No Unique : No |
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Description : Mitotic count / 5mm² observed by the experts pathologists during the national reviewing
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ID : 1066
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : Tumour spillage confirmed by several experts pathologists during the national reviewing
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Possible values :
Yes, No, Unknown |
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ID : 1061
Type : Constrained Content : TEXT Mandatory : No Multiple values : No Unique : No |
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Description : AFIP classification calculated by several experts pathologists during the national reviewing
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Possible values :
Very low risk, Low risk, Intermediate risk, High risk |
| Version 5.4.1-SNAPSHOT |