A rare case report on complete cervical agenesis with vaginal atresia and suspended didelphys uterus with hematometra and left haematosalpinx

Simple item page
dc.contributor.authorDwivedi, Divyaen_US
dc.contributor.authorJain, Madhuen_US
dc.contributor.authorJain, Shuchien_US
dc.contributor.authorJain, Shivien_US
dc.date.accessioned2020-10-16T08:03:12Z
dc.date.available2020-10-16T08:03:12Z
dc.date.issued2020-03
dc.description.abstractCongenital uterine malformations are deviations from normal anatomy resulting due to defective fusion of Mullerian ducts or the paramesonephric ducts in the developing embryo. These anomalies may be isolated or in combination with urological abnormalities. The mean prevalence of female congenital malformations in general population is up to ⁓ 7%. Patients with these anomalies usually present during pubertal age due to absence of onset of menses, cyclical abdominal pain, or in reproductive age group as infertility or recurrent pregnancy loss depending upon the degree of malformation. Cervical agenesis is a rare Mullerian anomaly with an incidence of 1 in 80,000 females. It represents 3% of all uterine anomalies. It is rarely associated with a functioning uterus (4.8%). Cervical agenesis is often associated with vaginal atresia (less than 50%). It is important to classify these anomalies for easy diagnosis and plan appropriate preoperative treatment.en_US
dc.identifier.affiliationsDepartment of Obstetrics and Gynecology, Trauma Centre, IMS, Banaras Hindu University, Varanasi, Uttar Pradesh, Indiaen_US
dc.identifier.affiliationsDepartment of Obstetrics and Gynecology, IMS, Banaras Hindu University, Varanasi, Uttar Pradesh, Indiaen_US
dc.identifier.affiliationsDepartment of Radiology, IMS, Banaras Hindu University, Varanasi, Uttar Pradesh, Indiaen_US
dc.identifier.citationDwivedi Divya, Jain Madhu, Jain Shuchi, Jain Shivi. A rare case report on complete cervical agenesis with vaginal atresia and suspended didelphys uterus with hematometra and left haematosalpinx. International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 2020 Mar; 9(3): 1274-1277en_US
dc.identifier.issn2320-1770
dc.identifier.issn2320-1789
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/207543
dc.languageenen_US
dc.publisherMedip Academyen_US
dc.relation.issuenumber3en_US
dc.relation.volume9en_US
dc.source.urihttps://dx.doi.org/10.18203/2320-1770.ijrcog20200914en_US
dc.subjectCervical agenesisen_US
dc.subjectCONUTA classificationsen_US
dc.subjectSuspensory uterusen_US
dc.subjectVaginal atresiaen_US
dc.titleA rare case report on complete cervical agenesis with vaginal atresia and suspended didelphys uterus with hematometra and left haematosalpinxen_US
dc.typeJournal Articleen_US
Files
Original bundle
Now showing 1 - 1 of 1
Thumbnail Image
Name:
ijrcog2020v9n3p1274.pdf
Size:
292.18 KB
Format:
Adobe Portable Document Format
Download
Collections
International Journal of Reproduction, Contraception, Obstetrics and Gynecology