Results 1 to 10 of about 1,436 (213)

Hematocolpos due to lower vaginal agenesis in an adolescent girl

open access: yesAcute Medicine & Surgery, 2023
Background Hematocolpos due to imperforate hymen is an important differential diagnosis of abdominal pain in early adolescent stage. However, hematocolpos due to lower vaginal agenesis must be considered because the management differs.
Kazunori Imai   +2 more
exaly   +3 more sources

A rare cause of amenorrhea: Hematocolpos in a post‐cystocele repair patient [PDF]

open access: yesClinical Case Reports
Key Clinical Message Secondary hematocolpos is a rare but serious complication after cystocele repair. This warrants multidisciplinary management (gynecology and urology) to optimize outcomes & minimize iatrogenic risks. Abstract Hematocolpos is the term
Tibyan Noorallah Mohammed   +2 more
doaj   +3 more sources

Incidental diagnosis of genital tuberculosis in a prepubertal girl presenting with acute urinary retention: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Genital tuberculosis affecting prepubertal girls is extremely uncommon, posing a great diagnostic challenge. It is a form of extrapulmonary tuberculosis usually seen in the reproductive age group.
Priyanka Garg   +2 more
doaj   +2 more sources

Complete transverse vaginal septum complicated by pyocolpos, primary vesicoureteral reflux and ectopic ureter with renal loss: a case report [PDF]

open access: yesUrology Case Reports
A transverse vaginal septum is a rare Müllerian anomaly caused by incomplete fusion between the Müllerian ducts and the urogenital sinus. It can obstruct menstrual flow, leading to hematocolpos, hydrocolpos, or pyocolpos.
Izadora Gabriela Coutinho   +5 more
doaj   +2 more sources

Congenital Abnormalities Causing Hematocolpos: A Pictorial Essay [PDF]

open access: yesJournal of the Belgian Society of Radiology
Hematocolpos, characterized by the accumulation of menstrual blood in the vagina, is a rare condition often misdiagnosed due to its uncommon occurrence and non-specific symptoms.
Louise Dorthu, Denis Danthine
doaj   +2 more sources

Rare Presentation of Imperforate Hymen in a 16‐Year‐Old: A Case Report From Nepal [PDF]

open access: yesClinical Case Reports
Imperforate hymen should be suspected in adolescent girls presenting with primary amenorrhea and cyclic abdominal or pelvic pain. Early genital examination is essential for timely diagnosis.
Dipendra Jung Shahi   +4 more
doaj   +2 more sources

Herlyn Werner Wunderlich Syndrome with Hematocolpos Symptom [PDF]

open access: yesOpen Access Macedonian Journal of Medical Sciences, 2019
BACKGROUND: Uterodidelphys with obstructed hemivagina and ipsilateral renal agenesis is referred to as the Herlyn Werner Wunderlich (HWW) syndrome.
Rambe, Andrina Yunita Murni   +2 more
core   +5 more sources

Severe Abdominal Pain Mimicking Appendicitis Caused by Imperforate Hymen: Case Report and Narrative Review [PDF]

open access: yesPediatric Reports
An imperforate hymen is a rare congenital genital anomaly causing menstrual blood retention during puberty. Treatment consists of a simple surgical incision of the hymenal membrane.
Julia Kleina   +5 more
doaj   +2 more sources

Delayed diagnosis of Herlyn-Werner-Wunderlich syndrome with diffuse adenomyosis in bilateral horns [PDF]

open access: yesRadiology Case Reports
The Herlyn-Werner-Wunderlich syndrome is a rare congenital disorder with uterus didelphys, unilateral obstructed hemivagina and ipsilateral renal agenesis, more common on right side. HWW syndrome usually presents at puberty with symptoms like pelvic pain,
Roshna Adhikari   +4 more
doaj   +2 more sources

Successful pregnancy in a woman with Herlyn-Werner-Wunderlich syndrome: A case report and literature review [PDF]

open access: yesCase Reports in Women's Health
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital condition characterized by renal agenesis, uterine didelphys, and obstructed hemivagina. This report presents the case of a 19-year-old woman who reported lower abdominal pain and offensive ...
Anas R. Tuqan   +6 more
doaj   +2 more sources

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