Ljubić A, Sulović V, Stanković A, Cvetković A
Clinique de Gynécologie et d'Obstétrique, Centre Clinique Universitaire, Belgrade, Yougoslavie.
J Gynecol Obstet Biol Reprod (Paris). 1993;22(4):417-8.
The failure of urorectal septum to form and divide the cloaca into rectum dorsally, and urogenital sinus ventrally, results in a cloacal dysgenesis. It is an extremely rare anatomic malformation of the genito-urinary tract and alimentary tract. A case of pregnancy and vaginal delivery in a patient with cloacal dysgenesis type II and previous heart operation is presented. Both mother and newborn were in good condition. The way of treatment of such patients is discussed.
尿直肠隔未能形成并将泄殖腔背侧分隔为直肠、腹侧分隔为泌尿生殖窦,会导致泄殖腔发育不全。这是一种极其罕见的泌尿生殖道和消化道解剖畸形。本文报道了一例患有II型泄殖腔发育不全且曾接受心脏手术的患者怀孕及阴道分娩的病例。母婴情况均良好。文中讨论了此类患者的治疗方式。