Pencitraan Radiologis Uterus Didelphys

Estherolita Dewi, Wawan Kustiawan
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Abstract

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
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子宫放射成像
子宫双侧畸形是指妊娠6-11周子宫、宫颈和阴道形成过程中出现的勒氏管合并失败的先天性疾病,属于III型勒氏管异常,即子宫、宫颈和阴道存在不相连的重复。2012年子宫白喉的发病率估计为1:3000名妇女。胆管异常可通过超声(USG)、磁共振成像(MRI)和子宫输卵管造影(HSG)等影像学检查观察。HSG可以显示勒氏管异常,但不能区分勒氏管异常本身的类型,而USG和MRI显示能够更详细地看到解剖
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