An interesting case of Herlyn–Werner–Wunderlich syndrome

Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital anomaly characterized by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Usually, such patients present with dysmenorrhea shortly after menarche, increasing pelvic pain and a palpable mass due to the obstructed hemi...

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Main Author: Maureen P Tigga
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Tzu-Chi Medical Journal
Subjects:
Online Access:http://www.tcmjmed.com/article.asp?issn=1016-3190;year=2020;volume=32;issue=2;spage=216;epage=218;aulast=Tigga
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author Maureen P Tigga
author_facet Maureen P Tigga
author_sort Maureen P Tigga
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description Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital anomaly characterized by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Usually, such patients present with dysmenorrhea shortly after menarche, increasing pelvic pain and a palpable mass due to the obstructed hemivagina. Interestingly in the present case, the patient had her menarche seven years ago, but dysmenorrhea started only 1-year back. She never sought medical help previously as she was mostly asymptomatic all through the years. It was only after she conceived and got investigated for antenatal concerns that she was found to have HWWS. A tortuous history and an unusual clinical presentation made this case an interesting one.
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spelling doaj.art-b3c3d39f9b324b11b70bdfad2b9e242d2022-12-21T23:31:41ZengWolters Kluwer Medknow PublicationsTzu-Chi Medical Journal1016-31902223-89562020-01-0132221621810.4103/tcmj.tcmj_13_19An interesting case of Herlyn–Werner–Wunderlich syndromeMaureen P TiggaHerlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital anomaly characterized by uterus didelphys with blind hemivagina and ipsilateral renal agenesis. Usually, such patients present with dysmenorrhea shortly after menarche, increasing pelvic pain and a palpable mass due to the obstructed hemivagina. Interestingly in the present case, the patient had her menarche seven years ago, but dysmenorrhea started only 1-year back. She never sought medical help previously as she was mostly asymptomatic all through the years. It was only after she conceived and got investigated for antenatal concerns that she was found to have HWWS. A tortuous history and an unusual clinical presentation made this case an interesting one.http://www.tcmjmed.com/article.asp?issn=1016-3190;year=2020;volume=32;issue=2;spage=216;epage=218;aulast=Tiggaherlyn–werner–wunderlich syndromemullerian duct anomalypandora's box
spellingShingle Maureen P Tigga
An interesting case of Herlyn–Werner–Wunderlich syndrome
Tzu-Chi Medical Journal
herlyn–werner–wunderlich syndrome
mullerian duct anomaly
pandora's box
title An interesting case of Herlyn–Werner–Wunderlich syndrome
title_full An interesting case of Herlyn–Werner–Wunderlich syndrome
title_fullStr An interesting case of Herlyn–Werner–Wunderlich syndrome
title_full_unstemmed An interesting case of Herlyn–Werner–Wunderlich syndrome
title_short An interesting case of Herlyn–Werner–Wunderlich syndrome
title_sort interesting case of herlyn werner wunderlich syndrome
topic herlyn–werner–wunderlich syndrome
mullerian duct anomaly
pandora's box
url http://www.tcmjmed.com/article.asp?issn=1016-3190;year=2020;volume=32;issue=2;spage=216;epage=218;aulast=Tigga
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