A case report demonstrates the challenge of diagnosing renal PEComa in a post-menopausal female, highlighting the importance of early detection.
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.
No takes yet. Share an insight, caveat, or question.
Kamble et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: