Primary bladder perivascular epithelioid cell tumour in an early adolescent

Francesca Gigola1,2, Charlotte Mussini3, Geraldine Héry4

  • 1Paediatric Surgery Unit, Université Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Hopital Bicetre, Le Kremlin-Bicetre, Île-de-France, France francesca.gigola@unifi.it.

BMJ Case Reports
|December 8, 2025
PubMed

Insights

Primary bladder perivascular epithelioid cell tumours (PEComas) are rare. This study highlights a PEComa case in an adolescent male with unusual symptoms, emphasizing PEComa diagnosis in pediatric patients.

Area of Science:

  • Urology
  • Oncology
  • Pathology

Background:

  • Primary bladder perivascular epithelioid cell tumours (PEComas) are rare neoplasms.
  • PEComas typically affect individuals in their third or fourth decade of life.
  • Diagnosis relies on radiological and histopathological findings, with surgical excision as the primary treatment.

Purpose of the Study:

  • To report a rare case of primary bladder PEComa in an adolescent male.
  • To highlight the importance of considering PEComa in pediatric patients with specific symptoms.
  • To discuss the diagnostic and clinical implications of this rare tumor presentation.

Main Methods:

  • Case report presentation.
  • Review of clinical presentation, radiological imaging, and histopathological findings.
  • Discussion of diagnostic considerations and treatment approaches.

Main Results:

  • A primary bladder PEComa was diagnosed in an early adolescent male.
  • The patient presented with macroscopic haematuria and a hypervascular bladder mass.
  • This presentation is atypical given the typical age demographic for PEComas.

Conclusions:

  • Primary bladder PEComa can occur in pediatric patients.
  • Macroscopic haematuria and hypervascular bladder mass are key indicators for considering PEComa.
  • Early consideration of PEComa is crucial for timely diagnosis and management in younger populations.