Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report.


Journal

JNMA; journal of the Nepal Medical Association
ISSN: 1815-672X
Titre abrégé: JNMA J Nepal Med Assoc
Pays: Nepal
ID NLM: 0045233

Informations de publication

Date de publication:
29 Feb 2024
Historique:
received: 28 02 2024
medline: 2 10 2024
pubmed: 2 10 2024
entrez: 2 10 2024
Statut: epublish

Résumé

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.

Identifiants

pubmed: 39356778
doi: 10.31729/jnma.8520
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

214-216

Auteurs

Saurav Sen Oli (SS)

Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal.

Shova Sapkota (S)

Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal.

Rupa Bajagain (R)

Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal.

Rachana Saha (R)

Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal.

Suman Paudel (S)

Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal.

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Classifications MeSH