Matsui Futoshi, Shimada Kenji, Matsumoto Fumi, Obara Takashi
Department of Urology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
J Pediatr Surg. 2008 Dec;43(12):2285-7. doi: 10.1016/j.jpedsurg.2008.08.004.
We report herein a case of resolution of severe megacystis, possibly caused by spontaneous rupture of posterior urethral valves during follow-up on a prenatal ultrasound. A 32-year-old woman presented at gestational week 15 for evaluation of fetal bladder enlargement. Prenatal ultrasonography revealed megacystis and posterior urethral dilatation. The longitudinal diameter of the bladder was 25 mm. Megacystis spontaneously resolved at gestational week 16. No association with urinary ascites was observed, and amniotic fluid volume remained normal throughout gestation. A boy was delivered vaginally at week 37. Apgar scores were 8 at 1 minute and 9 at 5 minutes. The neonate voided smoothly. Ultrasonography revealed a thickened bladder wall and normal kidneys and upper urinary tracts. Voiding cystourethrography showed dilatation of the posterior urethra but confirmed normal bladder capacity with smooth voiding and no vesicoureteral reflux. On day 57, remnant valves were incised. Postoperatively, filling cystometry showed a compliant bladder with no involuntary phasic contraction. At 7 months follow-up, the infant was asymptomatic, and ultrasonography showed some improvement of bladder wall thickness. Resolution of megacystis in utero appears to have resulted from spontaneous rupture of the posterior urethral valves. To the best of our knowledge, no similar cases have been previously reported.
我们在此报告一例严重巨膀胱症消退的病例,可能是由于产前超声随访期间后尿道瓣膜自发破裂所致。一名32岁女性在妊娠15周时因胎儿膀胱增大前来评估。产前超声检查发现巨膀胱和后尿道扩张。膀胱纵径为25毫米。巨膀胱症在妊娠16周时自发消退。未观察到与尿腹水相关,且整个孕期羊水量保持正常。一名男婴在37周时经阴道分娩。阿氏评分1分钟时为8分,5分钟时为9分。新生儿排尿顺利。超声检查显示膀胱壁增厚,肾脏和上尿路正常。排尿性膀胱尿道造影显示后尿道扩张,但证实膀胱容量正常,排尿顺畅且无膀胱输尿管反流。在第57天时,切开残余瓣膜。术后,充盈性膀胱测压显示膀胱顺应性良好,无自主性节律性收缩。在7个月的随访中,婴儿无症状,超声检查显示膀胱壁厚度有所改善。子宫内巨膀胱症的消退似乎是由于后尿道瓣膜自发破裂所致。据我们所知,此前尚无类似病例报道。