Open AccessPencitraan Radiologis Uterus Didelphys
Author(s) -
Estherolita Dewi,
Wawan Kustiawan
Publication year - 2019
Publication title -
jurnal radiologi indonesia (indonesian journal of radiology)
Language(s) - English
Resource type - Journals
eISSN - 2656-5803
pISSN - 2443-1745
DOI - 10.33748/jradidn.v3i2.66
Subject(s) - uterus didelphys , mullerian ducts , hysterosalpingography , müllerian mimicry , uterus , cervix , medicine , vagina , magnetic resonance imaging , duct (anatomy) , gynecology , mesonephric duct , anatomy , radiology , infertility , biology , pathology , pregnancy , kidney , cancer , genetics
Uterus didelphys is a congenital disorder in which there is a failure of merging of the Müllerian duct, during formation of uterine, cervix, and vagina at 6-11 weeks of gestation, which belongs to type III müllerian duct abnormalities, where there is unconnected duplication of the uterus, cervix and vagina. Incidence of uterine didelphys in 2012 is estimated 1: 3000 women. Müllerian duct abnormalities can be observed by imaging such as Ultrasonography (USG), Magnetic Resonance Imaging (MRI) and hysterosalpingography (HSG). The HSG can show the müllerian duct abnormalities, but cannot distinguish the type of the müllerian duct abnormalities themselves, whereas those on USG and MRI are shown to be able to see antomic in more detail