Angiolipoleiomyóm maternice.
Kazuistika a prehľad literatúry

Czech version

Authors: K. Kajo ¹; P. Žúbor ²; Š. Krivuš ¹; J. Danko ²
Authors‘ workplace: Ústav patologickej anatómie Jesseniovej lekárskej fakulty Univerzity Komenského a Martinskej fakultnej nemocnice, Martin, vedúci prof. MUDr. L. Plank, CSc. ¹; Gynekologicko-pôrodnícka klinika Jesseniovej lekárskej fakulty Univerzity Komenského a Martinskej fakultnej nemocnice, Martin, vedúci prof. MUDr. J. Danko, CSc. ²
Published in: Ceska Gynekol 2010; 75(1): 54-56

Overview

Objective:
The rare case presentation of angiolipoleiomyoma (ALLM) of the uterus with review of diagnostic and discriminative information for this entity.

Subject:
Case report with review of the literature.

Setting:
Department of Pathology and Obstetrics and Gynecology at Jessenius Medical Faculty in Martin.

Conclusion:
The ALLM of the uterus is rare benign mixed mesenchyme tumor consisting of smooth muscle bundles, foci of mature fat tissue and abnormal vessels.

The presented case is describing a 53-year-old women hysterectomized for multiple uterine myoma of which two showed the histological signs of ALLM. On imunohistochemical profile are these tumors negative for melanocytic features, e.g. HMB-45, what distinguishes them from angiomyolipomas, which are currently categorized into so called PEComas –⁠ tumors originating from perivascular epithelial cells.

Key words:
uterus, leiomyoma, angiolipoleiomyoma, angiomyolipoma, PEComa.

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