Back to Search Start Over

A rare case of perivascular epithelioid cell tumor (PEComa) of the greater omentum

Authors :
Koichi Okamoto
Yuka Okada
Kohei Ohno
Takahiro Yagi
Mitsuo Tsukamoto
Takuya Akahane
Ryu Shimada
Tamuro Hayama
Takeshi Tsuchiya
Keijiro Nozawa
Keiji Matsuda
Tsuyoshi Ishida
Fukuo Kondo
Yojiro Hashiguchi
Source :
World Journal of Surgical Oncology, Vol 16, Iss 1, Pp 1-5 (2018)
Publication Year :
2018
Publisher :
BMC, 2018.

Abstract

Abstract Background A tumor composed exclusively or predominantly of human melanin black 45 (HMB45)-positive epithelioid cells is called a perivascular epithelioid cell tumor (PEComa). We report a very rare case of a PEComa of the greater omentum. Case presentation MRI conducted to examine the orthopedic disease of the patients, a 49-year-old Japanese woman, also identified a tumor in her pelvis. A CT scan revealed a tumor mass on the right side of the pelvic floor and clear nutrient vessels originating from the splenic and celiac arteries. An omental primary tumor or accessory spleen was thus suspected, and tumor resection was performed. The tumor was a light brown solid tumor with a smooth margin, measuring 5.2 × 3.8 × 3.5 cm. Histopathologically, the tumor was composed mainly of spindle and epithelioid cells, and large and small blood vessel formation was observed. In the immunohistochemical staining, tumor cells were positive for human melanin black 45 (HMB-45) and Melan-A and partially positive for alpha-smooth muscle actin. The final diagnosis was PEComa of the greater omentum. Conclusions Although omental PEComa is very rare, it should be considered as a differential disease of an omental primary tumor.

Details

Language :
English
ISSN :
14777819
Volume :
16
Issue :
1
Database :
Directory of Open Access Journals
Journal :
World Journal of Surgical Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.5ba83bc7f87e4601864e1144ed3a5394
Document Type :
article
Full Text :
https://doi.org/10.1186/s12957-018-1407-5