后尿道瓣膜与前尿道瓣膜、前尿道大憩室及尿道下裂的罕见关联。

Q4 Medicine Journal of Endourology Case Reports Pub Date : 2020-12-29 eCollection Date: 2020-01-01 DOI:10.1089/cren.2020.0138
Prashant Jain, Ashish Prasad, Sarika Jain
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引用次数: 0

摘要

背景:多发性尿道异常是一种罕见的疾病,在诊断和治疗方面具有挑战性。由于近端梗阻掩盖了远端梗阻的早期诊断,双尿道梗阻常被漏诊。我们报告一例罕见的后尿道瓣膜(PUV)和前尿道瓣膜(AUV)合并前尿道憩室(AUD)和尿道下裂的病例。病例介绍:一个11个月大的男婴在puv电灼后持续出现泌尿系统症状。他随后被发现有远端尿道梗阻,原因是AUV和尿道前球憩室大。他还伴有腺状尿道下裂。他接受了内镜下AUV消融和憩室切除术。结论:尿道下裂合并PUV、AUV、AUD是罕见的。在这种多发性异常的情况下,诊断和治疗可能具有挑战性。为了避免误诊,需要高度的怀疑,适当的尿道造影评估和详细的膀胱尿道镜检查。
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A Rare Association of Posterior Urethral Valve with Anterior Urethral Valve, Large Anterior Urethral Diverticula, and Glanular Hypospadias.

Background: Multiple urethral anomalies are rare with its own challenges in diagnosis and management. The double urethral obstructions are often missed as proximal obstruction can mask the early diagnosis of distal obstruction. We present a rare case of concomitant posterior urethral valve (PUV) and anterior urethral valve (AUV) with a large anterior urethral diverticula (AUD) and hypospadias. Case Presentation: An 11-month-old male child after fulguration of PUVs continued to have urinary symptoms. He was subsequently found to have distal urethral obstruction because of AUV and large anterior urethral bulbar diverticula. He also had associated glanular hypospadias. He was managed with endoscopic ablation of AUV and diverticulectomy. Conclusion: Concomitant PUV, AUV, AUD, and hypospadias is a rare occurrence. The diagnosis and management can be challenging in such cases with multiple anomalies. To avoid a misdiagnosis, a high index of suspicion, proper assessment of urethrogram, and detailed cystourethroscopy is required.

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