EPITHELOID TYPE RENAL ANGIOMYOLIPOMA

被引：0

作者：

Faydaci, Gokhan ^{[1
]}

Uruc, Fatih ^{[1
]}

Murtazaoglu, Medine ^{[2
]}

Tarhan, Fatih ^{[1
]}

Eryildirim, Bilal ^{[1
]}

Kuyumcuoglu, Ugur ^{[1
]}

机构：

[1] Dr Lutfi Kirdar Kartal Egitim & Arastirma Hastane, Urol Klin, Istanbul, Turkey

[2] Dr Lutfi Kirdar Kartal Egitim & Arastirma Hastane, Patol Klin, Istanbul, Turkey

来源：

TURKISH JOURNAL OF UROLOGY | 2007年 / 33卷 / 03期

关键词：

Angiomyolipoma; Epitheloid angiomyolipoma; Renal cell carcinoma;

D O I：

暂无

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Introduction: Angiomyolipoma (AML) is a well-known rare soft tissue tumor involving the kidneys, liver and other organs. For a long time believed to be a benign hamartoma, angiomyolipoma is now considered a neoplasm that arises from perivascular epitheloid cell. Epitheloid angiomyolipoma is a rare variant of angiomyolipoma characterized by epitheloid cells that mimic renal cell carcinoma and it is potentially malignant. Immunreactivity with HMB45 and CD68 are helpful for its identification. We report a multifocal epitheloid angiomyolipoma case with prominent pleomorphism and necrosis and reviewed literature.

引用

页码：357 / 359

页数：3

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