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先天性无阴道患者的泌尿生殖系统异常

Urologic and genital anomalies in patients with congenital absence of the vagina.

作者信息

Fore S R, Hammond C B, Parker R T, Anderson E E

出版信息

Obstet Gynecol. 1975 Oct;46(4):410-6.

PMID:1165875
Abstract

Forty-three patients with primary amenorrhea secondary to congenital absence of the vagina have been seen at this institution over the past 25 years. Associated urologic anomalies were present in 47% of patients in whom evaluation of the urinary tract was performed. Two patients recently presented with the rare combination of vaginal agenesis and solitary pelvic kidney, and one other such patient was found in a retrospective study of these records. A review of the literature concerning the associations of these conditions is presented with reference to frequency, embryology, pathophysiology, diagnostic methods, and various surgical procedures for correction of vaginal agenesis. The results of surgical correction using simple techniques in this institution have been comparable to those of other authors. The need for thorough preoperative evaluation of patients with genital malformations to include complete urologic studies is stressed.

摘要

在过去25年里,本机构共接诊了43例因先天性无阴道继发原发性闭经的患者。在接受泌尿系统评估的患者中,47%存在相关泌尿系统异常。最近有2例患者表现出阴道发育不全与孤立性盆腔肾这种罕见的组合,在对这些记录的回顾性研究中又发现了1例此类患者。本文参考了这些病症关联的发生频率、胚胎学、病理生理学、诊断方法以及矫正阴道发育不全的各种外科手术方法,对相关文献进行了综述。本机构采用简单技术进行手术矫正的结果与其他作者的结果相当。强调了对生殖器畸形患者进行全面术前评估的必要性,包括完整的泌尿系统检查。

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