Literature DB >> 26025488

Spontaneous Ruptured Uterus in an Adolescent With Polycystic Ovarian Syndrome and Endometrial Hyperplasia.

Mary Anne Baquing1, Joy Brotherton2.   

Abstract

Uterine diverticula and rudimentary horns are rare forms of uterine anomalies that occur during embryogenesis. They can communicate with the endometrial cavity and may have the potential to develop pathology. This case report presents an obese, anovulatory adolescent with polycystic ovarian syndrome who was admitted with acute abdominal pain and found to have radiological findings that were concerning for a ruptured mass contiguous with the uterine cavity, which was likely a uterine horn or diverticulum. Further evaluation revealed simple hyperplasia without atypia on endometrial sampling, supporting the surgical resection and subsequent medical management of this young patient.
Copyright © 2015 AAGL. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adolescent; Endometrial hyperplasia; Polycystic Ovary Syndrome; Uterine diverticula; Uterine horn; Uterine rupture

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Year:  2015        PMID: 26025488     DOI: 10.1016/j.jmig.2015.05.014

Source DB:  PubMed          Journal:  J Minim Invasive Gynecol        ISSN: 1553-4650            Impact factor:   4.137


  1 in total

1.  Successful pregnancy and vaginal delivery after laparoscopic excision of a congenital uterine cervical diverticulum: A case report.

Authors:  Keiko Tanaka; Naomi Shiga; Takashi Kuno; Zen Watanabe; Masahito Tachibana; Nobuo Yaegashi
Journal:  J Obstet Gynaecol Res       Date:  2020-04-12       Impact factor: 1.730

  1 in total

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