A case of communicating uteri, i.e., two separate uterus bodies, double cervix, double vagina unilaterally blind, with the characteristic feature of a short communication between the two uterine cavities as well as the two vaginae is reported. This condition arises from the arrest of fusion and canalization of the Müllerian ducts. It is manifested by irregular bleeding and potential dystocia in case of pregnancy. Unilateral renal agenesis is a concomitant feature of this rare genital malformation.
报道了一例交通性子宫病例，即两个独立的子宫体、双宫颈、单侧盲端双阴道，其特征是两个子宫腔以及两个阴道之间存在短的交通。这种情况源于苗勒管融合和管道化的停滞。其表现为不规则出血，妊娠时可能出现难产。单侧肾缺如是这种罕见生殖器畸形的伴随特征。
