Uterovaginal duplication with blind hemivagina and ipsilateral renal agenesis: Review of unusual presentation

被引:12
|
作者
Takagi, H. [2 ]
Matsunami, K. [2 ]
Imai, A. [1 ]
机构
[1] Matsunami Gen Hosp, Inst Endocrine Related Canc, Gifu 5016062, Japan
[2] Matsunami Gen Hosp, Dept Obstet & Gynaecol, Gifu 5016062, Japan
关键词
Herlyn-Werner-Wunderlich syndrome; Mullerian anomaly; pyometrocolpos; renal agenesis; WERNER-WUNDERLICH-SYNDROME; UTERUS DIDELPHYS; OBSTRUCTED HEMIVAGINA; MALFORMATIONS; HEMATOCOLPOS; HEMATOMETRA; MANAGEMENT; ANOMALIES;
D O I
10.3109/01443611003763416
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Congenital abnormalities of the Mullerian duct system can result in various urogenital anomalies, including uterus didelphys with blind hemivagina and ipsilateral renal agenesis (Herlyn-Werner-Wunderlich syndrome). It usually presents after the menarche with progressive pelvic pain during periods secondary to haematocolpos. However, rarely presentation is unusual with consequent diagnostic delay. This paper attempts to review the medical literature for rare presentations that make diagnosis and treatment difficult, including our cases. Clinicians must be aware of the importance of this rare congenital anomaly of the female genital tract, especially many years after the menarche. This condition should be considered to prevent misdiagnosis or suboptimal treatment.
引用
收藏
页码:350 / 353
页数:4
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