一个青少年的巨大先天性膀胱憩室:通过一个特殊的治疗挑战来导航一个不寻常的临床实体-一个病例报告

IF 0.4 Q4 UROLOGY & NEPHROLOGY
W. Salama , M. Tetou , M. Mrabti , M.A. Sobhi , A. Elbahri , M. Alami , A. Ameur
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引用次数: 0

摘要

原发性先天性膀胱憩室,罕见的儿科人群,特别是在女性,往往证明手术的症状病例。我们报告一个15岁的女孩,她有巨大的膀胱憩室,明显的空后残余尿,肾功能保留,无膀胱输尿管反流。由于家庭拒绝手术,保守治疗包括抗生素预防、监测成像和生活方式改变。观察到临床稳定性(减少感染,无并发症)和解剖稳定性,支持残留肌肉纤维作为稳定因素的假设,提示可能的疾病重新分类。这个病例强调了个性化的治疗决定,包括家庭偏好和严格的监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Massive congenital bladder diverticulum in a teenager: Navigating an uncommon clinical entity through an exceptional therapeutic challenge – A case report
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.
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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