García González P, Meana Morís A R, Gracía Chapullé A, Matesanz Pérez J L
Servicio de Radiodiagnóstico, Hospital de Cabueñes, Gijón, España.
Radiologia. 2009 Mar-Apr;51(2):194-7. doi: 10.1016/j.rx.2009.01.001. Epub 2009 Mar 9.
We report a case of uterus didelphys with blind hemivagina and ipsilateral renal agenesis. This is an uncommon anomaly of the development of the Mullerian ducts in which a defect in one of the Wolffian ducts leads to failed induction in kidney formation and in the fusion of the Mullerian ducts. MRI plays a decisive role in the diagnosis and characterization of the malformation.
我们报告一例双子宫伴盲端半阴道及同侧肾缺如的病例。这是中肾管发育的一种罕见异常,其中一条沃尔夫管的缺陷导致肾脏形成及中肾管融合诱导失败。MRI在该畸形的诊断和特征描述中起决定性作用。