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赫林-韦纳-温德利希综合征中的异位尿道开口:一项罕见发现。

Ectopic urethral opening in herlyn-werner-wunderlich syndrome: A rare finding.

作者信息

Akhlaque Eesha, Hassan Muhammad Faateh, Akhlaque Irum

机构信息

Department Of Radiology, Lahore Medical and Dental College, Tulspura, North Canal Rd, Lahore, Punjab, Pakistan.

Department of Radiology, Mayo Hospital, King Edward Medical College, Neela Gumbad Chowk, Lahore, Punjab, Pakistan.

出版信息

Radiol Case Rep. 2024 Sep 25;19(12):6339-6342. doi: 10.1016/j.radcr.2024.08.056. eCollection 2024 Dec.

Abstract

Recorded findings of Herlyn-Werner-Wunderlich Syndrome (HWWS) remain sparse due to low statistical incidence. Ours is also the first known case to present with an ectopic urethral opening, an even rarer complication. A 27-year-old nulliparous woman presented with complaints of cyclical hematuria, and burning micturition with intermittent episodes of urinary retention suprapubic and pelvic pain. After extensive radiological examination, the MRI findings concluded the presence of a uterine didelphys with 2 cervixes and vaginal duplication marked by the compression of the left hemivagina and dilation of the right hemivagina, pointing towards HWWS. The case strongly suggests that the presence of an ectopic urethral opening may be the cause of urinary incontinence and discomfort in an otherwise asymptomatic patient of HWWS.

摘要

由于统计发病率较低,关于赫林-韦纳-温德利希综合征(HWWS)的记录发现仍然很少。我们的病例也是已知首例出现异位尿道开口的情况,这是一种更为罕见的并发症。一名27岁未生育的女性,主诉周期性血尿、排尿烧灼感,伴有间歇性耻骨上和盆腔疼痛及尿潴留。经过广泛的影像学检查,MRI结果显示存在双子宫、双宫颈以及阴道重复畸形,表现为左半阴道受压、右半阴道扩张,提示为HWWS。该病例强烈表明,异位尿道开口的存在可能是HWWS无症状患者出现尿失禁和不适的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a4/11462045/906507d3599e/gr1.jpg

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