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CASE REPORT

Epithelioid angiomyolipoma associated with a classic angiomyolipoma

Seiichi Kato1, Kensaku Seike1, Takako Masue2, Naoki Yamamoto3, Shinichi Maeda1

1 Department of Urology, Toyota Memorial Hospital, Toyota, Japan
2 Department of Urology, Gifu University Hospital, Gifu, Japan
3 Department of Primary Care, Shinsei Hospital, Nagano, Japan
Address correspondence to Dr. Naoki Yamamoto, Department of Primary Care, Shinsei Hospital, 851 Obuse, Obuse-chou, Kamitakaigun, Nagano, Japan 381-0295

Canadian Journal of Urology 2009, 16(5), 4857-4859.

Abstract

We report a case of renal epithelioid angiomyolipoma that arose in association with a classic angiomyolipoma in a 54-year-old Japanese man without tuberous sclerosis. Histologically, the tumor was composed of polygonal cells exhibiting diffuse hemorrhage, multifocal necroses, and vascular invasion. Immunohistochemical staining was positive for melanoma specifi c antibody and focally positive for smooth muscle actin. On the basis of a review of the literature, we suggest that large epithelioid angiomyolipoma may have malignant potential and therefore requires close follow up.

Keywords

epithelioid angiomyolipoma, malignant potential

Cite This Article

APA Style
Kato, S., Seike, K., Masue, T., Yamamoto, N., Maeda, S. (2009). Epithelioid angiomyolipoma associated with a classic angiomyolipoma. Canadian Journal of Urology, 16(5), 4857–4859.
Vancouver Style
Kato S, Seike K, Masue T, Yamamoto N, Maeda S. Epithelioid angiomyolipoma associated with a classic angiomyolipoma. Can J Urology. 2009;16(5):4857–4859.
IEEE Style
S. Kato, K. Seike, T. Masue, N. Yamamoto, and S. Maeda, “Epithelioid angiomyolipoma associated with a classic angiomyolipoma,” Can. J. Urology, vol. 16, no. 5, pp. 4857–4859, 2009.



cc Copyright © 2009 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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