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Tumores retroperitoneales primitivos del adulto (página 3)

Enviado por pablo

Partes: 1, 2, 3

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    Anexo 1. Clasificación OMS / 2002, tumores partes blandas.

    Tejido adiposo

    • Benigno

    ICD-O (726)*





    Lipomatosis del nervio(nerviosa)








    Lipoma condroide


    Angiomyolipoma extrarenal


    Myelolipoma extra adrenal


    Células fusiformes - pleomorfico




    • Intermedio (localmente agresivo)

    Tumor lipomatoso atípico / liposarcoma bien diferenciado


    • Maligno

    Liposarcoma desdiferenciado


    Liposarcoma mixoide


    Liposarcoma células redondas


    Liposarcoma pleomorfico


    Liposarcoma tipo mixto


    Liposarcoma sin otra especificación


    Tumor fibroblastico - myofibroblastico

    • Benigno

    Fascitis nodular

    Fascitis proliferativa

    Myositis proliferativa

    Myositis osificante

    Fascitis isquémica



    Hamartoma fibroso de la infancia



    Fibromatosis colli

    Fibromatosis hialina juvenil

    Fibromatosis de cuerpos de inclusión

    Fibroma vaina tendinosa


    Fibroblastoma desmoplastico


    Myofibroblastoma tipo mamario


    Fibroma calcificante aponeurótico




    Angiofibroma celular


    Fibroma tipo nucal


    Fibroma Gardner


    Tumor fibroso calcificante

    Angiofibroma células gigantes


    • Intermedio (localmente agresivo)

    Fibromatosis superficial (plantar - palmar)


    Fibromatosis tipo desmoide


    • Intermedio (raramente metastizante)

    Tumor fibroso solitario y hemangiopericitoma

    8815/1 - 9150/1

    Tumor myofibroblastico inflamatorio


    Sarcoma myofibroblastico bajo grado


    Sarcoma fibroblastico mixoinflamatorio


    Fibrosarcoma infantil


    • Maligno

    Fibrosarcoma del adulto




    Sarcoma fibromixoide de bajo grado -

    Tumor de células redondas


    Fibrosarcoma epitelioide esclerosante


    Tumor tipo fibrohistocitario


    Tumor de la vaina tendinosa de células gigantes


    Células gigantes tipo difuso


    Histocitoma fibroso profundo benigno


    Intermedio (raramente metastatizante)

    Tumor fibrohistocitico plexiforme


    Tumor células gigantes



    Histocitoma fibroso maligno pleomorfico - sarcoma indiferenciado pleomorfico


    Histocitoma fibroso maligno células gigantes - sarcoma pleomorfico indiferenciado con células gigantes


    Histocitoma fibroso maligno inflamatorio - sarcoma pleomorfico indiferenciado con inflamación prominente.


    Tumores musculo liso



    Leiomioma profundo


    Leiomioma genital




    Tumores Pericitico (perivascular)

    Tumor glomus

    Tumor glomus maligno




    Tumores del musculo esquelético



    Tipo adulto

    Tipo fetal

    Tipo genital






    Rabdomiosarcoma embrionario (células redondas, botroide, anaplasico)




    Rabdomiosarcoma alveolar (solido, anaplasico)


    Rabdomiosarcoma pleomorfico


    Tumores vasculares



    • Capilar

    • Cavernoso

    • Arteriovenoso

    • Venoso

    • Intramuscular

    • Sinovial








    Hemangioma epitelioide





    Intermedio (localmente agresivo)

    hemangioendotelioma Kaposiforme


    Intermedio (raramente metastatizante)

    Hemangioendotelioma retiforme


    Angioendotelioma papilar intralinfatico


    Hemangioendotelioma compuesto


    Sarcoma de Kaposi



    Hemangioendotelioma epitelioide


    Angiosarcoma partes blandas


    Tumores condro- oseos

    Condroma partes blandas


    Condrosarcoma mesenquimatico


    Osteosarcoma extraesqueletico


    Tumores de diferenciación incierta


    Mixoma intramuscular (incluye variedad celular)


    Mixoma yuxta-articular


    Angiomixoma profundo (agresivo)


    Tumor angioestasico hialinizante pleomorfico

    Thimoma hamartomatoso ectópico


    Intermedio (raramente metastatizante)

    Histocitoma fibroso angiomatoide


    Tumor fibromixoide osificante (atípico-maligno)


    Tumor mixoide - mioepitelioma - paracondroma





    Sarcoma sinovial


    Sarcoma epitelioide


    Sarcoma partes blandas alveolar


    Sarcoma partes blandas células claras


    Condrosarcoma mixoide extraesqueletico


    PNET/Extraesqueletico Ewing tumor PNET



    Tumor desmoplasico de células redondas


    Tumor rabdoide extrarenal


    Mesenquimoma maligno


    PEComa. Neoplasma con diferenciación celular perivascular epitelioide - tumor miomelanocitico células claras

    Sarcoma intimal


    *Código de la clasificación internacional de enfermedades oncológicas.






    Dr Pablo Valsangiácomo

    Clínica Quirúrgica 3. Prof Dr Luis Ruso.

    Hospital Maciel. Facultad de Medicina.

    Montevideo. Uruguay

    Junio 2011

    Partes: 1, 2, 3

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