ArticleRadiology case reports2026
Epithelioid PEComa coexisting with angiomyolipoma in the kidney.
Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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
2 citing papers in PubMed.
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4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Renal epithelioid perivascular epithelioid cell tumors (PEComas) are rare neoplasms with potential for aggressive clinical behaviour that present a significant diagnostic challenge due to imaging features that overlap with renal cell carcinoma (RCC). We present the case of a 51-year-old female with the coexistence of a typical fat-containing renal angiomyolipoma (AML) and an adjacent large, fat-poor renal mass on computed tomography (CT), confirmed on histopathology as an epithelioid PEComa, with high-risk features including large size and necrosis. Despite complete resection, a local recurrence of the PEComa was detected in the surgical bed 14 months postoperatively. This case serves as a clinical example of the rare but recognized association between classic AML and epithelioid PEComa. Furthermore, the recurrence also reinforces the necessity of diligent long-term surveillance following the resection of such tumors, especially in cases with high risk features.
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