ArticleIndian journal of surgical oncology2022
Perivascular Epithelioid Cell Tumor (PEComa) of Vulva: a Rare Occurrence.
Article in Indian journal of surgical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Sclerosing Perivascular Epithelioid Cell Tumor of the Uterus: A Rare Entity Posing Diagnostic Challenge.Journal of mid-life healthArticle
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6 authors.
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Abstract
Perivascular epithelioid cell tumor (PEComa) is a tumor of mesenchymal origin, with features of perivascular epithelioid cells. The primary sites of PEComa reported are the uterus, vulva, rectum, heart, breast, urinary bladder, abdominal wall, pancreas, retroperitoneum, liver, and uterus. But what is unique is that PEComa of the gynecological tract is very rare. Uterus is the most common location of PEComa reported from female genital tract. PEComa of vulva is extremely rare. A 36-year-old woman presented with vulvar mass. Her final histopathological report came as PECOMA. Ours is the third case of PEComa vulva reported in English literature. After extensive literature search, we found only two previous cases reported of PEComa of vulva. One case was of primary PEcoma of vulva reported from Japan and other from China. Distinguishing among mesenchymal neoplasms, including PEComas, endometrial stromal sarcomas, and leiomyosarcomas, can be difficult. Careful analysis of morphologic and immunohistochemical features is of the utmost importance. Ours is the third such case of PEComa of vulva reported in English literature.
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