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A Case of Malignant PEComa of the Uterus Associated with Intramural Leiomyoma and Endometrial Carcinoma

Authors
Choi, Yoo JinHong, Jin HwaKim, AereeKim, HankyeomChang, Hyeyoon
Issue Date
11월-2016
Publisher
KOREAN SOCIETY PATHOLOGISTS
Keywords
Immunihistochemistry; Perivascular epithelioid cell neoplasms; Uterus
Citation
JOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE, v.50, no.6, pp.469 - 473
Indexed
SCOPUS
KCI
Journal Title
JOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE
Volume
50
Number
6
Start Page
469
End Page
473
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/86946
DOI
10.4132/jptm.2016.04.20
ISSN
2383-7837
Abstract
Perivascular epithelioid cell tumors (PEComas) refers to a family of mesenchymal neoplasms composed of angiomyolipomas, clear cell "sugar" tumors of the lung, and lymphangioleiomyomatoses. These tumors have a distinctive and common component of perivascular epithelioid cells that show an association with blood vessel walls and immunohistochemically display myomelanocytic differentiation. The unique neoplasms have been shown to have an expanded range through a variety of case reports, including visceral, intra-abdominal, soft tissue, and bone tumors. The retroperitoneum, abdominopelvic region, and uterus have been reported to be the most common sites. Most PEComas follow a benign course. However, reports of malignant PEComas are increasing. Many papers have described uterine PEComas, but to our knowledge, there have not yet been any reports of a malignant PEComa arising concomitant with another epithelial tumor and mesenchymal tumor. We report herein the case of a 67-year-old woman who experienced a malignant uterine PEComa infiltrating a preexisting intramural leiomyoma with synchronous well differentiated endometrial carcinoma and multiple liver and lung metastases.
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