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罕见的苗勒管异常:完全纵隔子宫合并阴道纵膈与横膈

Rare Müllerian Anomaly: Complete Septate Uterus with Simultaneous Longitudinal and Transverse Vaginal Septa.

作者信息

Louden Erica D, Awonuga Awoniyi O, Gago Laura A, Singh Manvinder

机构信息

Wayne State University School of Medicine/Detroit Medical Center, Detroit, Michigan.

Wayne State University School of Medicine/Detroit Medical Center, Detroit, Michigan.

出版信息

J Pediatr Adolesc Gynecol. 2015 Dec;28(6):e189-91. doi: 10.1016/j.jpag.2015.04.012. Epub 2015 May 9.

Abstract

BACKGROUND

We present a patient with primary amenorrhea and a rare combination of anomalies. She was found to have a septate uterus, double cervix, and a longitudinal and a low transverse vaginal septum.

CASE

An 18-year-old girl with primary amenorrhea presented with severe monthly pelvic pain. Examination and imaging revealed a thin transverse vaginal septum, complete septate uterus, double cervix, and a longitudinal vaginal septum. The transverse and longitudinal vaginal septa were excised and repaired.

SUMMARY AND CONCLUSION

Although repetitive pregnancy loss and preterm birth are associated with various Müllerian duct anomalies, clinicians should also be suspicious of the presented anomaly in cases of primary amenorrhea and cyclic pelvic pain. To our knowledge, this is the only case of simultaneous septate uterus with longitudinal and transverse vaginal septum and the second case of combined longitudinal and transverse septum, which caused primary amenorrhea. This rare anomaly further supports the bidirectional regression theory of Müllerian development.

摘要

背景

我们报告一名患有原发性闭经且伴有罕见异常组合的患者。她被发现有纵隔子宫、双宫颈以及纵向和低位横向阴道纵隔。

病例

一名18岁原发性闭经女孩,每月出现严重盆腔疼痛。检查和影像学显示有薄的横向阴道纵隔、完全纵隔子宫、双宫颈以及纵向阴道纵隔。切除并修复了横向和纵向阴道纵隔。

总结与结论

虽然反复流产和早产与各种苗勒管异常有关,但对于原发性闭经和周期性盆腔疼痛的病例,临床医生也应怀疑存在本文所述的异常情况。据我们所知,这是唯一一例同时存在纵隔子宫与纵向和横向阴道纵隔的病例,也是第二例由纵向和横向纵隔联合导致原发性闭经的病例。这种罕见的异常情况进一步支持了苗勒管发育的双向退化理论。

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