Results 1 to 10 of about 3,414 (117)

Surgical management of an obstructive Müllerian Anomaly in a patient with anorectal malformation [PDF]

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Müllerian duct anomalies are rare in the general population, occurring in less than 3% of women, but much more prevalent in female patients with anorectal malformation, occurring in up to 30% of these patients.
Christina M. Theodorou   +4 more
doaj   +2 more sources

Ovarian dysgerminoma with Müllerian anomaly: a case report [PDF]

open access: yesObstetrics & Gynecology Science, 2020
Müllerian anomalies are rare deformities in women, and only a few cases concerning gynecologic malignancies arising in patients with congenital uterine malformations have been reported. Herein, we present the case of a 34-year-old woman with dysgerminoma
Ha Na Kim   +8 more
doaj   +2 more sources

Incidental discovery of persistent Müllerian duct syndrome with transverse testicular ectopia during adult inguinal hernia repair: A case report [PDF]

open access: yesUrology Case Reports
Transverse testicular ectopia (TTE) associated with persistent Müllerian duct syndrome (PMDS) is a rare congenital anomaly that may remain undiagnosed until adulthood.
Zubair Mohamed Dahir Sed   +4 more
doaj   +2 more sources

A novel AMHR2 gene mutation causing transverse testicular ectopia: A rare case report and literature review [PDF]

open access: yesUrology Case Reports
Transverse testicular ectopia (TTE) is a rare anomaly often associated with persistent Müllerian duct syndrome and infertility. We report a 34-year-old man with primary infertility, a vacant right hemiscrotum, and a left scrotal mass.
Tien Dung Mai Ba   +5 more
doaj   +2 more sources

Delayed diagnosis of a non-communicating right uterine horn: A case report and literature review

open access: yesCase Reports in Women's Health, 2023
Background: Accurate diagnosis of a müllerian anomaly is essential for appropriate management and prevention of complications. However, diagnosis is often missed or delayed.
Lindsay A. Hartup   +2 more
doaj   +1 more source

Complete Uterine Septum with Duplicate Cervix, Longitudinal Vaginal Septum and Unilateral Vaginal Obstruction (Herlyn-Werner-Wunderlich Syndrome): A Case Report of a Mullerian Duct Anomaly [PDF]

open access: yesWomen’s Health Bulletin, 2021
Introduction:Herlyn-Werner-Wunderlich Syndrome (HWWs) is a rare variant of Mullerian duct anomalies. It is associated with a wide range of gynecological and obstetric complications, such as urinary incontinence, urinary retention, endometriosis, pelvic ...
Leili Hafizi   +2 more
doaj   +1 more source

Rare presentation of hematometrocolpos with didelphys uterus in a teenager

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Hematometrocolpos is one of the rare Mullerian anomaly presenting as abdominal pain during the age of menarche. We present a case of 14 year old girl presenting with amenorrhea to our hospital with imperforate hymen who on examination and investigation ...
P. Vedak, D.B. Bhusare, P. Patil
doaj   +1 more source

An atypical Müllerian duct anomaly: Duplicated cervices and vaginas with a single uterine cavity

open access: yesRadiology Case Reports, 2023
Müllerian duct anomalies include a wide variety of developmental abnormalities involving the female reproductive system, many of which are not adequately represented by the current classification system used in the United States.
Ryan Narbutas, MD   +4 more
doaj   +1 more source

Juvenile cystic adenomyoma, a rare diagnostic challenge: Case Reports and literature review

open access: yesF&S Reports, 2021
Objective: To report 2 very rare cases of young women who presented with severe dysmenorrhea and a large cystic lesion in the myometrium, which presented a diagnostic dilemma because they were confused with a Müllerian anomaly. Design: Case reports and a
Sushila Arya, M.D., M.S.   +1 more
doaj   +1 more source

Complex mullerian malformation: A rare case of hypoplastic noncavitated uterus in the middle with two rudimentary horns on either side

open access: yesJournal of Human Reproductive Sciences, 2020
Mullerian anomalies which cause infertility in women were described by different classification systems. We report a rare case of uterine anomaly in a 16-year-old patient presented with primary amenorrhea. Her diagnostic laparoscopy findings revealed two
Kamala Selvaraj   +2 more
doaj   +1 more source

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