Year: 2025
Type: article
Study design: Case Report
Abstract: Background: gene. It is characterized by developmental delay, hair abnormalities, hypotonia, and organ dysfunction. Bladder diverticula are a rare but recognized urological complication, and its rupture can lead to severe clinical consequences. Methods: We report a case of a 3-year-old boy diagnosed with Menkes syndrome, presenting with multiple bladder diverticula and diverticular rupture, resulting in acute abdominal effusion. The patient underwent excision of multiple bladder diverticula guided by imaging and urodynamic evaluation. Postoperative functional recovery was assessed through follow-up imaging and urodynamic studies. Results: Postoperative urodynamic parameters showed significant improvement. Follow-up revealed satisfactory voiding function without evidence of recurrence or increased residual urine. Imaging and urodynamic studies were instrumental in both preoperative localization and postoperative functional assessment. Conclusions: Early diagnosis and surgical excision of bladder diverticula in patients with Menkes syndrome can significantly improve prognosis. Imaging and urodynamic studies provide reliable support for comprehensive management and are invaluable for long-term postoperative follow-up.
Source: Frontiers in Pediatrics
Authors: Guoxing Wu, Pengfei Gao, Wenbin Zhang, Honghui Li, Zhaoying Li, Zhaoying Li, Ruifa Wu, Zuoqing Li, Zuoqing Li, Mingchuan Huang, Zhe Xu
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,801
OpenAlex ID: W4412041742