A Rare Presentation of Herlyn Werner Wunderlich Disease in Young Female

Authors

  • Nicola Zampieri

Abstract

Background: Herlyn-Werner-Wunderlich syndrome is a rare urogenital anomaly consisted of renal agenesia, uterovaginal duplication and ipsilateral blind hemivagina. Usually it presents some months after menarche with pelvic pain, acute abdomen, intermenstrual bleeding.

Case report: A 13 year premenarchal female was transferred to our unit for acute abdomen and MR findings of left renal agenesis, blind hemivagina distended by ematic material, complete uterus duplication , dilated tuba and left ovarian mass with torsion. A diagnostic laparoscopy was performed during which detorsion of the ovarian tubal complex was performed with resection of ovarian cyst.

Summery and Conclusion: This is a rare syndrome and ovarian torsion is never reported as complication

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Published

2020-05-20

How to Cite

Zampieri, N. (2020). A Rare Presentation of Herlyn Werner Wunderlich Disease in Young Female. Archives of Clinical and Medical Case Reports, 4(3), 500–503. Retrieved from https://fortunejournals.org/ojs/index.php/acmcr/article/view/22338