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青少年巨大先天性膀胱憩室:通过一项特殊治疗挑战应对一种罕见临床病症——病例报告

Massive congenital bladder diverticulum in a teenager: Navigating an uncommon clinical entity through an exceptional therapeutic challenge - A case report.

作者信息

Salama W, Tetou M, Mrabti M, Sobhi M A, Elbahri A, Alami M, Ameur A

机构信息

Mohamed V University of Rabat, Faculty of Medicine, Morocco.

Hassan II University of Casablanca, Faculty of Medicine, Morocco.

出版信息

Urol Case Rep. 2025 Jul 21;62:103139. doi: 10.1016/j.eucr.2025.103139. eCollection 2025 Sep.

Abstract

Primary congenital bladder diverticula, rare in pediatric populations and particularly in females, often justify surgery for symptomatic cases. We report a 15-year-old girl with a giant bladder diverticulum, significant post-void residual urine, and preserved renal function without vesicoureteral reflux. Conservative care included antibiotic prophylaxis, surveillance imaging, and lifestyle modifications was adopted due to family refusal of surgery. Clinical stability (reduced infections, no complications) and anatomical stability were observed, supporting the hypothesis of residual muscular fibers as a stabilizing factor, suggesting potential nosological reclassification. This case underscores individualized therapeutic decisions integrating family preferences and rigorous monitoring.

摘要

原发性先天性膀胱憩室在儿科人群中罕见,在女性中尤为如此,有症状的病例通常需要手术治疗。我们报告了一名15岁女孩,患有巨大膀胱憩室、大量排尿后残余尿量,且肾功能正常,无膀胱输尿管反流。由于家属拒绝手术,采取了包括抗生素预防、监测成像和生活方式调整在内的保守治疗。观察到临床稳定(感染减少,无并发症)和解剖稳定,支持残余肌纤维作为稳定因素的假说,提示可能需要重新分类疾病。该病例强调了结合家庭偏好和严格监测的个体化治疗决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f94/12311440/c8d29da17e25/gr1.jpg

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