Sporadic perivascular epithelioid cell tumor of the wall of the jejunum: A case report


COD: 3076_206_06_2019_ep Categorie: , ,

Antonio Giuliani, Lucia Romano, Vincenzo Vicentini, Alessandra Di Sibio,
Giuseppe Calvisi, Virginia Ciuffetelli, Mario Schietroma, Francesco Carlei

Ann Ital Chir, Digital Edition 2019, 8
Epub, June 26

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BACKGROUND: Perivascular epithelioid cell tumors are rare mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. They are considered ubiquitous tumors and have been described in different organs, but gastro-intestinal PEComas are diseases of extreme rarity.
METHODS: We report a case of a 51-year-old woman, without a medical history of tuberous sclerosis complex, affected by abdominal PEComa, adhering tightly to the jejunal loop and to the spleen.
RESULTS: During the surgical operation, a large abdominal mass was found, and surgical resection was carried out.
Definitive histologic and ultrastructural findings were consistent with PEComa.
CONCLUSION: Given the rarity of GI-PEComas and the lack of cases reported in the literature, we want to emphasize the importance of conducting further studies in this regard, to better describe their biological behaviour.


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