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    Soft-tissue extrarenal rhabdoid tumor with a unique long-term survival.

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    Authors
    Fabre, A
    Eyden, Brian P
    Ali, H H
    Affiliation
    Histopathology Department, St Mary's Hospital, London, UK.
    Issue Date
    2004
    
    Metadata
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    Abstract
    Rhabdoid tumors of kidney and extrarenal rhabdoid tumors are identified by a round-epithelioid cell morphology and a bland immunophenotype, but a distinctive ultrastructure dominated by paranuclear whorls of intermediate filaments, most usually of vimentin. These tumors are also known to be highly aggressive malignancies, which, typically, bear a poor prognosis, frequently measured in months following initial presentation. The authors record the case a soft-tissue rhabdoid tumor in a 12-year-old boy with a unique long-term survival in excess of 16 years. The features of this case are documented, with a brief summary of histological, immunohistochemical, ultrastructural, and genetic characteristics of this entity.
    Citation
    Soft-tissue extrarenal rhabdoid tumor with a unique long-term survival. 2004, 28 (1):49-52 Ultrastruct Pathol
    Journal
    Ultrastructural Pathology
    URI
    http://hdl.handle.net/10541/84406
    PubMed ID
    14967599
    Type
    Article
    Language
    en
    ISSN
    0191-3123
    Collections
    All Christie Publications

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