A rare presentation of bilateral synchronous renal tumours misdiagnosed as tuberculosis

A 32-year-old woman with dialysis-requiring kidney failure presented with constitutional symptoms and bilateral kidney masses and was initially diagnosed with renal tuberculosis (TB). However, despite TB treatment, her condition deteriorated, leading to a right nephrectomy. Histopathological examina...

Full description

Saved in:
Bibliographic Details
Main Authors: Debi M. Moagi, Busiswa F. Bisiwe
Format: Article
Language:English
Published: AOSIS 2025-02-01
Series:South African Journal of Oncology
Subjects:
Online Access:https://sajo.org.za/index.php/sajo/article/view/311
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:A 32-year-old woman with dialysis-requiring kidney failure presented with constitutional symptoms and bilateral kidney masses and was initially diagnosed with renal tuberculosis (TB). However, despite TB treatment, her condition deteriorated, leading to a right nephrectomy. Histopathological examination revealed the presence of embryonal rhabdomyosarcoma (ERMS), a rare malignancy typically seen in paediatric populations. Alternative diagnoses, even rare ones like ERMS, should be considered when dealing with bilateral kidney masses. Radical nephrectomy remains the primary treatment for ERMS, but adjuvant therapies may also be beneficial. Contribution: This case highlights the diagnostic challenges of bilateral kidney masses and the importance of considering rare malignancies in the differential diagnosis. Prompt histopathological evaluation is crucial for accurate diagnosis and timely management.
ISSN:2518-8704
2523-0646