Multinucleated Giants: Unveiling Pediatric Renal Epithelioid PEComa

Perivascular epithelioid cell tumors (PEComas) of the kidney are rare mesenchymal tumors that rarely occur in children. Individuals with tuberous sclerosis (TS) are at increased risk for these tumors. While classic PEComas are benign, the epithelioid variant could have malignant potential and metastasis capacity. We report a case of right kidney epithelioid PEComa with uncertain malignant potential in a 3-year-old girl who had no personal or family history of tuberous sclerosis. The tumor was found through ultrasound imaging. Sections from the radical nephrectomy specimen showed epithelioid and spindle cells with abundant granular eosinophilic or clear cytoplasm, mildly pleomorphic vesicular nuclei and distinctive perivascular arrangement. Abundant multinucleated giant cells were seen. No further therapy was suggested by the oncologist. The patient is doing well ten months post-surgery. We reviewed the literature and analyzed the features of pediatric renal PEComas reported so far.

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Publication Details

Journal
Fetal and Pediatric Pathology
Published
2025-02-21
DOI
https://doi.org/10.1080/15513815.2025.2458677
Primary Topic
Tuberous Sclerosis Complex Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Multinucleated Giants: Unveiling Pediatric Renal Epithelioid PEComa

Mohammad Vasei, Aileen Azari-Yam, Moeinadin Safavi
Fetal and Pediatric Pathology
Tuberous Sclerosis Complex Research
article

Multinucleated Giants: Unveiling Pediatric Renal Epithelioid PEComa

Mohammad Vasei, Aileen Azari-Yam, Moeinadin Safavi
article en

Abstract

Perivascular epithelioid cell tumors (PEComas) of the kidney are rare mesenchymal tumors that rarely occur in children. Individuals with tuberous sclerosis (TS) are at increased risk for these tumors. While classic PEComas are benign, the epithelioid variant could have malignant potential and metastasis capacity. We report a case of right kidney epithelioid PEComa with uncertain malignant potential in a 3-year-old girl who had no personal or family history of tuberous sclerosis. The tumor was found through ultrasound imaging. Sections from the radical nephrectomy specimen showed epithelioid and spindle cells with abundant granular eosinophilic or clear cytoplasm, mildly pleomorphic vesicular nuclei and distinctive perivascular arrangement. Abundant multinucleated giant cells were seen. No further therapy was suggested by the oncologist. The patient is doing well ten months post-surgery. We reviewed the literature and analyzed the features of pediatric renal PEComas reported so far.

Fetal and Pediatric PathologyVol. 44(2)
Shariati Hospital (IR), Children's Medical Center (IR), Tehran University of Medical Sciences (IR)
Zero hunger
Openalex Percentile: Top 96%
Tuberous Sclerosis Complex Research
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