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首页> 外文期刊>Female pelvic medicine & reconstructive surgery >Subpubic cartilaginous cyst presenting as acute urinary retention: A report and review of the literature
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Subpubic cartilaginous cyst presenting as acute urinary retention: A report and review of the literature

机译:表现为急性尿retention留的耻骨下软骨囊肿:报告和文献复习

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摘要

Introduction: A subpubic cartilaginous cyst is a rare and therefore poorly understood pathologic process involving the symphysis pubis. We describe a case of a postmenopausal female with acute urinary retention secondary to a periurethral cyst, and provide a literature review of previously reported cases of women with presenting complaints of a vulvar mass or pain. The differential diagnoses of a subpubic cartilaginous cyst, as well as management options, are discussed. Case: A 68-year-old woman presented with acute urinary retention. Physical examination revealed a 4-cm tender cystic mass palpated along the anterior vaginal wall traversing toward the posterior pubic ramus. A pelvic magnetic resonance imaging showed a 4.4 × 3.5 × 4.2-cm3 wellcircumscribed, cystic lesion at the anterior aspect of the lower urethra with no intrinsic contrast enhancement. The cyst was surgically excised through a transvaginal approach with no recurrence to date. Conclusions: A subpubic cartilaginous cyst is an uncommon lesion thought to originate from the symphysis pubis and to be a result of degenerative changes. Patients have presented with pain, a vulvar/vaginal mass, or both. This case describes a patient who presented with acute urinary retention. In patients with suspected subpubic cartilaginous cyst, the lesion may be excised in symptomatic patient or observed in those who are asymptomatic. Standard of care has not yet been determined regarding management due to the rarity of the lesion.
机译:简介:耻骨下软骨囊肿是罕见的,因此涉及耻骨联合的病理过程了解甚少。我们描述了绝经后女性继发于尿道周围囊肿并伴有急性尿retention留的病例,并提供了对先前报道的女性患者外阴肿块或疼痛的报道的文献综述。讨论了耻骨下软骨囊肿的鉴别诊断以及治疗方案。病例:一名68岁的女性出现急性尿retention留。体格检查发现,沿着前阴道壁触及耻骨后壁的部位触诊了一个4厘米长的嫩囊性肿块。骨盆磁共振成像显示在下尿道的前部有4.4×3.5×4.2-cm3的界限分明的囊性病变,没有内在的对比增强。囊肿经阴道手术切除,至今未复发。结论:耻骨下软骨囊肿是一种罕见的病变,被认为起源于耻骨联合,并且是变性改变的结果。患者出现疼痛,外阴/阴道肿块或两者兼有。该病例描述了出现急性尿retention留的患者。在怀疑患有耻骨下软骨囊肿的患者中,病变可在有症状的患者中切除或在无症状的患者中观察到。由于病变的稀有性,尚未确定治疗的护理标准。

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