Epiteloid Tip Renal Anjiyomiyolipom

Anjiyomyolipom (AML) böbrek, karaciğer ve diğer organları tutabilen ender görülen ve iyibilinen bir yumuşak doku tümörüdür. Epiteloid anjiyomyolipom değişik derecelerde nükleeratipi ve yoğun eozinofilik stoplazmalı poligonal hücrelerin varlığı ile karakterize yenitanımlanmış bir anjiyomyolipom türüdür. HMB-45 ve CD68 immünreaktivitesi tanıdayardımcıdır. Bu makalede 19 yaşında bir bayan hastadaki epiteloid tip AML olgusunu bildirdik

Epitheloid Type Renal Angiomyolipoma

Angiomyolipoma (AML) is a well-known rare soft tissue tumor involving the kidneys, liverand other organs. Epithelioid angiomyolipoma is a recently recognized variant ofangiomyolipoma, which is characterized by the presence of polygonal cells with denselyeosinophilic cytoplasm and varying degrees of nuclear atypia. Immunreactivity with HMB-45and CD68 are helpful for its identification. We report a case of epithelioid angiomyolipoma ofthe kidney that occurred in a 19-year-old woman

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