Results 11 to 20 of about 613 (115)

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

open access: yesClin Case Rep
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 used for the accumulation of menstrual blood in the vagina.
Mohammed TN, Elgadi A, Nuri GME.
europepmc   +2 more sources

Routine 36-week scan: diagnosis of fetal abnormalities. [PDF]

open access: yesUltrasound Obstet Gynecol
ABSTRACT Objectives To investigate further the incidence and types of fetal abnormality identified at a routine 36‐week ultrasound examination, which had not been diagnosed in previous scans at 20 weeks and 12 weeks' gestation, and to report the fetal abnormalities that are diagnosed only postnatally.
Syngelaki A   +5 more
europepmc   +2 more sources

Hematocolpos due to lower vaginal agenesis in an adolescent girl

open access: yesAcute Medicine &Surgery, Volume 10, Issue 1, January/December 2023., 2023
Hematocolpos due to vaginal agenesis with a functional uterus are particularly rare and are sometimes misdiagnosed in adolescent females because of the diversity in symptoms. Major complaints in cases diagnosed during adolescence are often lower abdominal pain, back pain, cancelation dysfunction, and primary amenorrhea.
Kazunori Imai   +8 more
wiley   +1 more source

Forty‐two normomenstruating adolescents with Müllerian obstructive anomalies: Presentation, pitfalls in the dagnosis and surgical management

open access: yesActa Obstetricia et Gynecologica Scandinavica, Volume 102, Issue 1, Page 92-98, January 2023., 2023
Unilateral obstructive Müllerian anomalies are not uncommon in adolescents and pose a diagnostic and surgical challenge. Abstract Introduction We analyzed the frequency, presentation and pitfalls in the diagnosis and surgical management of a large group of normomenstruating adolescents with obstructive reproductive tract anomalies.
Eleonora Fontana   +5 more
wiley   +1 more source

Atypical phenotype of a patient with Bardet–Biedl syndrome type 4

open access: yesMolecular Genetics &Genomic Medicine, Volume 10, Issue 5, May 2022., 2022
Here, we report a patient with polydactyly, renal particularities, anal imperforation, and malformation of genitals in the context of 46,XY karyotype. Complex genital malformation and anal imperforation are not reported in male BBS4 patient to date.
Natacha Sloboda   +14 more
wiley   +1 more source

Primary amenorrhea secondary to imperforate hymen

open access: yesClinical Case Reports, Volume 10, Issue 4, April 2022., 2022
Hymen imperforation is uncommon. Symptoms include primary amenorrhea, a bulging perineal mass, cyclical abdominal pain, and urinary retention or infections. Clinical awareness allows an opportune diagnosis, thus preventing complications. Abstract Hymen imperforation is uncommon.
Hanae Ramdani   +6 more
wiley   +1 more source

Hymen and virginity: What every paediatrician should know

open access: yesJournal of Paediatrics and Child Health, Volume 58, Issue 3, Page 382-387, March 2022., 2022
Paediatricians may face the notion of ‘virginity’ in various situations while caring for children and adolescents, but are often poorly prepared to address this sensitive topic. Virginity is a social construct. Despite medical evidence that there is no scientifically reliable way to determine virginity, misconceptions about the hymen and its supposed ...
Dehlia Moussaoui   +2 more
wiley   +1 more source

Age‐dependent phenotypes of ovarian endometriomas

open access: yesReproductive Medicine and Biology, Volume 21, Issue 1, January/December 2022., 2022
Abstract Purpose To analyze the characteristics of the ovarian endometrioma (OE) across the life span of a woman. In the past, the OE has traditionally been viewed as a single, monolithic disease. Today, there are emerging data indicating that OE phenotypes differ according to the age of the woman.
Giuseppe Benagiano, Sun‐Wei Guo
wiley   +1 more source

Obstetrical Challenges in Robinow Syndrome

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2022, Issue 1, 2022., 2022
Robinow syndrome is a genetically heterogenous syndrome that exhibits great pleiotropy, involving skeletal genital, cardiac, and craniofacial developmental anomalies. Fertility is not always compromised, and many individuals may be able to have a healthy pregnancy.
Yingao Zhang   +5 more
wiley   +1 more source

Pitfalls and challenges in managing neuroendocrine carcinoma of gynecological origin: A case series and brief review

open access: yesClinical Case Reports, Volume 9, Issue 5, May 2021., 2021
Due to gynecologic tract (gNET) rarity, gynecologists may not have a strong index of suspicion for which to diagnose these tumors ultimately causing misdiagnoses and potential mismanagement. Gynecologists should be wary of diagnostic pitfalls. Abstract Due to gynecologic tract (gNET) rarity, gynecologists may not have a strong index of suspicion for ...
Lauren E. Farmer   +2 more
wiley   +1 more source

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