Case report: Urachal perivascular epithelioid cell tumor

ConclusionsUrachal PEComa is a rare mesenchymal tumor that presents challenges in diagnosis through imaging and clinical symptoms. Definitive diagnosis relies on pathological and immunohistochemical analysis. Due to the rarity of urachal PEComa, prognosis assessment necessitates long-term follow-up and evaluation of more cases.
Source: Frontiers in Oncology - Category: Cancer & Oncology Source Type: research