From the spectrum of PEComa: a renal angiomyolipoma

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Authors: Shuvi V Kamble, Muhammad Umar Younis, Hemant J Vadeyar
Cited by: 1
References: 10

Abstract

PEComas or Perivascular Epithelioid Cell neoplasms are uncommon mesenchymal origin neoplasms composed of perivascular epithelioid cells. They affect various anatomic sites, kidneys being one of them. Renal PEComas are further rare, posing a challenge to include them in the differential diagnoses. We present a case of a type of renal PEComa in a 54-year old post-menopausal female with vague abdominal pain. Imaging revealed a large left perinephric mass initially suspected to be a liposarcoma. Surgical excision and subsequent histopathological evaluation confirmed a benign, fat predominant renal angiomyolipoma. This case depicts the mimicking and heterogenous nature of PEComas and the importance of early detection followed by appropriate treatment.

Fields of Study & Subjects

Tuberous Sclerosis Complex Research Renal cell carcinoma treatment Vascular Tumors and Angiosarcomas

Publication details

Journal / source
Journal of Surgical Case Reports
Publisher
Oxford University Press (OUP)
Volume
2026
Issue
4
Pages
rjag215–rjag215
Publication date
17 March 2026
Language
EN