Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report.
Humans
Female
Adolescent
Hydrocolpos
/ diagnosis
Vagina
/ abnormalities
Mullerian Ducts
/ abnormalities
Syndrome
Uterus
/ abnormalities
Abnormalities, Multiple
Ultrasonography
/ methods
Urogenital Abnormalities
/ complications
Wolffian Ducts
/ abnormalities
Drainage
/ methods
Flank Pain
/ etiology
Kidney
/ abnormalities
Gitelman syndrome
case reports
diabetes insipidus
hypokalemia nephrogenic.
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
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.
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM