Chelli H, Mazlout N, Abed A, Marzouki M M, Fadhlaoui A, Hendaoui L, Horchani A
Service de Gynécologie Obstétrique A, Centre de Maternité et de Néonatalogie, La Rabta, Tunis, Tunisie.
J Urol (Paris). 1996;102(5-6):240-2.
We report an exceptional case of pyeloureteral malformation which occurred on a single kidney. The malformation was discovered at 32 week of gestation when ultrasonography showed hydronephrosis. Initial treatment consisted in echoguided drainage. The patient gave birth to a live infant via normal vaginal delivery and then underwent resection of the pyeloureteral malformation with anastomotic reconstruction of the upper urinary tract.
我们报告了一例罕见的肾盂输尿管畸形病例,该畸形发生在单侧肾脏。畸形在妊娠32周时通过超声检查发现肾积水而被诊断。初始治疗为超声引导下引流。患者经正常阴道分娩产下一名活婴,随后接受了肾盂输尿管畸形切除术及上尿路吻合重建术。