Kato Yoshifumi, Yamataka Atsuyuki, Okazaki Tadaharu, Yanai Toshihiro, Lane Geoffrey J, Kobayashi Hiroyuki, Someya Tomonosuke, Yamashiro Yuichiro, Miyano Takeshi
Department of Pediatric General and Urogenital Surgery, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.
Pediatr Surg Int. 2006 Nov;22(11):911-3. doi: 10.1007/s00383-006-1763-z.
To study the surgical treatment and outcome of hydronephrosis secondary to pelviureteric junction obstruction (PUJS) that is so massive that the renal pelvis crosses over the vertebral column [mega-hydronephrosis (MH)]. Of the 40 cases of PUJS we treated over the past 5 years, 6 cases had MH secondary to PUJS (MH-PUJS) in 6 renal units and were reviewed. Incidence of MH was 15.0%. All had Anderson-Hynes dismembered pyeloplasty to treat obstructive renal pattern on technetium-99m diethylenetriaminepentaacetic acid (DTPA) scans in five and gait disturbance due to MH in one. The contralateral kidney was normal in five and dysplastic in one. Three had nephrostomy before pyeloplasty. Preoperative DTPA scans showed good renal function in four and poor in two. Plication of the entire dilated, lax renal parenchyma ("nephroplication") was performed in three to decrease the intra-renal pelvic cavity. Prenatal diagnosis was performed in three cases. Mean age at pyeloplasty was 3.5 years and mean duration of follow-up was 1.5 years. Postoperatively, two of the three who did not have nephroplication had prolonged but not obstructed renal pattern on DTPA scans, and the other case who did not have nephroplication had nephrectomy for non-functioning kidney caused by recurrent pyelonephritis 2 years after pyeloplasty. In the three who had nephroplication, DTPA scans showed acceptable to relatively good passage in all cases. The surgical treatment of MH-PUJS is challenging with no fixed guidelines. However, nephroplication may be useful during pyeloplasty to decrease the size of MH-PUJS.
研究继发于肾盂输尿管连接部梗阻(PUJS)且肾盂越过脊柱的巨大肾积水([巨肾积水(MH)])的手术治疗及预后。在过去5年我们治疗的40例PUJS患者中,6例6个肾单位存在继发于PUJS的MH(MH-PUJS)并进行了回顾性分析。MH的发生率为15.0%。所有患者均接受Anderson-Hynes离断性肾盂成形术,5例用于治疗99m锝二乙三胺五乙酸(DTPA)扫描显示的梗阻性肾图,1例因MH导致步态障碍。5例对侧肾正常,1例发育异常。3例在肾盂成形术前进行了肾造瘘。术前DTPA扫描显示4例肾功能良好,2例较差。3例对整个扩张、松弛的肾实质进行了折叠术(“肾折叠术”)以减小肾盆腔内空间。3例进行了产前诊断。肾盂成形术时的平均年龄为3.5岁,平均随访时间为1.5年。术后,3例未进行肾折叠术的患者中,2例DTPA扫描显示肾图延长但无梗阻,另1例未进行肾折叠术的患者在肾盂成形术后2年因复发性肾盂肾炎导致肾无功能而接受了肾切除术。在3例进行了肾折叠术的患者中,DTPA扫描显示所有病例均有可接受至相对良好的通过情况。MH-PUJS的手术治疗具有挑战性且没有固定的指导原则。然而,肾折叠术在肾盂成形术中可能有助于减小MH-PUJS的大小。