Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report
Herlyn-Werner-Wunderlich Syndrome is a very rare congenital malformation of the urogenital tract involving both the Mullerian and Wolffian ducts characterized by the triad uterine diadelphys, obstructed vagina, and unilateral renal agenesis. If not diagnosed on time it may progress to adverse gynec...
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Format: | Article |
Language: | English |
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Nepal Medical Association
2024-02-01
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Series: | Journal of Nepal Medical Association |
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Online Access: | https://jnma.com.np/jnma/index.php/jnma/article/view/8520 |
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author | Saurav Sen Oli Shova Sapkota Rupa Bajagain Rachana Saha Suman Paudel |
author_facet | Saurav Sen Oli Shova Sapkota Rupa Bajagain Rachana Saha Suman Paudel |
author_sort | Saurav Sen Oli |
collection | DOAJ |
description |
Herlyn-Werner-Wunderlich Syndrome is a very rare congenital malformation of the urogenital
tract involving both the Mullerian and Wolffian ducts characterized by the triad uterine diadelphys,
obstructed vagina, and unilateral renal agenesis. If not diagnosed on time it may progress to adverse
gynecological complications making timely diagnosis and treatment crucial. We hereby present a
14-year girl with right flank pain diagnosed as Herlyn-Werner-Wunderlich Syndrome by ultrasound
scan which was managed surgically with drainage of hydrocolpos and marsupialization of vaginal
septum. On two weeks follow up patient had symptomatic improvement with no any complications.
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first_indexed | 2024-03-07T19:08:52Z |
format | Article |
id | doaj.art-e5f39e769c8449969a8945c2654004ac |
institution | Directory Open Access Journal |
issn | 0028-2715 1815-672X |
language | English |
last_indexed | 2024-03-07T19:08:52Z |
publishDate | 2024-02-01 |
publisher | Nepal Medical Association |
record_format | Article |
series | Journal of Nepal Medical Association |
spelling | doaj.art-e5f39e769c8449969a8945c2654004ac2024-03-01T06:09:40ZengNepal Medical AssociationJournal of Nepal Medical Association0028-27151815-672X2024-02-016227110.31729/jnma.8520Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case ReportSaurav Sen Oli0Shova Sapkota1Rupa Bajagain2Rachana Saha3Suman Paudel4Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, NepalKathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, NepalKathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, NepalKathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal Herlyn-Werner-Wunderlich Syndrome is a very rare congenital malformation of the urogenital tract involving both the Mullerian and Wolffian ducts characterized by the triad uterine diadelphys, obstructed vagina, and unilateral renal agenesis. If not diagnosed on time it may progress to adverse gynecological complications making timely diagnosis and treatment crucial. We hereby present a 14-year girl with right flank pain diagnosed as Herlyn-Werner-Wunderlich Syndrome by ultrasound scan which was managed surgically with drainage of hydrocolpos and marsupialization of vaginal septum. On two weeks follow up patient had symptomatic improvement with no any complications. https://jnma.com.np/jnma/index.php/jnma/article/view/8520case reports; hydrocolpos; mullerian ducts; uterine didelphys. |
spellingShingle | Saurav Sen Oli Shova Sapkota Rupa Bajagain Rachana Saha Suman Paudel Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report Journal of Nepal Medical Association case reports; hydrocolpos; mullerian ducts; uterine didelphys. |
title | Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report |
title_full | Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report |
title_fullStr | Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report |
title_full_unstemmed | Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report |
title_short | Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report |
title_sort | herlyn werner wunderlich syndrome with hydrocolpos a case report |
topic | case reports; hydrocolpos; mullerian ducts; uterine didelphys. |
url | https://jnma.com.np/jnma/index.php/jnma/article/view/8520 |
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