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pubmed-article:11100813pubmed:abstractTextMalignant rhabdoid tumors are morphologically defined as sheets of loosely cohesive cells with eccentric nuclei and hyaline, paranuclear inclusions. Although originally described as a distinctive renal neoplasm of childhood, these tumors have since been described in all age groups and in a variety of extrarenal sites. In the latter setting, it is thought that the rhabdoid phenotype is comprised of histogenetically unrelated tumors, that regardless of histogenesis, pursue a biologically aggressive behavior.lld:pubmed
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pubmed-article:11100813pubmed:monthNovlld:pubmed
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pubmed-article:11100813pubmed:authorpubmed-author:StevensLLlld:pubmed
pubmed-article:11100813pubmed:authorpubmed-author:PattersonJJlld:pubmed
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pubmed-article:11100813pubmed:volume27lld:pubmed
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pubmed-article:11100813pubmed:pagination529-34lld:pubmed
pubmed-article:11100813pubmed:dateRevised2005-11-17lld:pubmed
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pubmed-article:11100813pubmed:articleTitleCutaneous epithelioid malignant nerve sheath tumor with rhabdoid features: a histologic, immunohistochemical, and ultrastructural study of three cases.lld:pubmed
pubmed-article:11100813pubmed:affiliationDepartment of Pathology, James Haley Veteran's Administration Hospital, Tampa, Florida, USA.lld:pubmed
pubmed-article:11100813pubmed:publicationTypeJournal Articlelld:pubmed
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