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Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review
Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital malformation characterized by uterus didelphys, unilateral blind hemivagina, and ipsilateral renal agenesis. The obstructed vagina affects menstrual flow, leading to related clinical symptoms after menarche. However, the age of onset, ini...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237300/ https://www.ncbi.nlm.nih.gov/pubmed/34194598 http://dx.doi.org/10.1016/j.radcr.2021.05.055 |
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author | Li, Xiaodan Liu, Tianzhu Li, Lina |
author_facet | Li, Xiaodan Liu, Tianzhu Li, Lina |
author_sort | Li, Xiaodan |
collection | PubMed |
description | Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital malformation characterized by uterus didelphys, unilateral blind hemivagina, and ipsilateral renal agenesis. The obstructed vagina affects menstrual flow, leading to related clinical symptoms after menarche. However, the age of onset, initial symptoms, and clinical complications differ among patients owing to the different types of vaginal septum. Herein, we report 2 cases. The first case is of a 20-year-old woman who presented with fever; she was diagnosed with vaginitis and pelvic inflammation due to the vaginal septum with ostiole. The second case is of a 12-year-old girl who complained of abdominal pain; she was diagnosed as having pelvic inflammation, omentitis, and suppurative appendicitis due to the atretic vaginal septum. |
format | Online Article Text |
id | pubmed-8237300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82373002021-06-29 Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review Li, Xiaodan Liu, Tianzhu Li, Lina Radiol Case Rep Case Report Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital malformation characterized by uterus didelphys, unilateral blind hemivagina, and ipsilateral renal agenesis. The obstructed vagina affects menstrual flow, leading to related clinical symptoms after menarche. However, the age of onset, initial symptoms, and clinical complications differ among patients owing to the different types of vaginal septum. Herein, we report 2 cases. The first case is of a 20-year-old woman who presented with fever; she was diagnosed with vaginitis and pelvic inflammation due to the vaginal septum with ostiole. The second case is of a 12-year-old girl who complained of abdominal pain; she was diagnosed as having pelvic inflammation, omentitis, and suppurative appendicitis due to the atretic vaginal septum. Elsevier 2021-06-20 /pmc/articles/PMC8237300/ /pubmed/34194598 http://dx.doi.org/10.1016/j.radcr.2021.05.055 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Li, Xiaodan Liu, Tianzhu Li, Lina Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review |
title | Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review |
title_full | Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review |
title_fullStr | Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review |
title_full_unstemmed | Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review |
title_short | Herlyn–Werner–Wunderlich syndrome and its complications: A report of two cases and literature review |
title_sort | herlyn–werner–wunderlich syndrome and its complications: a report of two cases and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237300/ https://www.ncbi.nlm.nih.gov/pubmed/34194598 http://dx.doi.org/10.1016/j.radcr.2021.05.055 |
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