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肾自体移植治疗中主动脉综合征所致肾血管性高血压。

Renal autotransplantation for renovascular hypertension caused by midaortic syndrome.

作者信息

Bleacher J, Turner M E, Quivers E, Schwartz M Z

机构信息

Department of Surgery, Children's National Medical Center, Washington, DC, USA.

出版信息

J Pediatr Surg. 1997 Feb;32(2):248-50; discussion 250-1. doi: 10.1016/s0022-3468(97)90188-3.

Abstract

Midaortic syndrome (MAS) is a well-recognized but rare cause of renovascular hypertension (RVH). Several techniques have been described to treat RVH caused by MAS. The authors recently treated two children with MAS and RVH. In both patients the right kidney had two renal arteries. A 13-year-old boy presented with severe headaches, pain in his lower extremities with exertion, and marked hypertension (blood pressure, 170/110). An aortogram demonstrated 70% narrowing of his abdominal aorta from the suprarenal region to 5 cm above the iliac bifurcation. There was significant stenosis of the celiac axis, superior mesenteric artery, and left renal artery. The right kidney had two renal arteries, and the upper pole artery was stenotic at its origin. A 10-year-old girl, known to have hypertension for several years had an aortogram that demonstrated 70% narrowing of the abdominal aorta from the suprarenal region to 3 cm above the iliac bifurcation. There was involvement of the left renal artery at its orifice. She also had two renal arteries to the right kidney with the right upper pole artery being stenotic at its origin and in the mid-portion of the vessel. Aortic reconstruction was accomplished with a polytetrafluoroehtylene (PTFE) bypass graft in each case. The first case also involved patch angioplasty of the celiac axis. In both cases, the right kidney was autotransplanted. It was removed intraoperatively, cold perfused, and the two renal arteries reconstructed followed by transplantation to the right iliac vessels. In both cases the left renal artery was reimplanted into the PTFE graft. Both patients had uncomplicated postoperative courses. The 13-year-old boy had evidence of renal ischemia in a portion of the lower pole of the autotransplanted kidney by DTPA scan. He has mild hypertension controlled with antihypertensive medication. The 10-year-old girl has a normal DTPA scan and is normotensive. MAS is a rare and challenging congenital vascular anomaly that causes RVH. In the presence of double renal arteries the technique of autotransplantation with cold perfusion and "bench" vascular reconstruction reduces the warm ischemia time and should produce satisfactory results.

摘要

中段主动脉综合征(MAS)是一种已被充分认识但罕见的肾血管性高血压(RVH)病因。已有多种技术被描述用于治疗由MAS引起的RVH。作者最近治疗了两名患有MAS和RVH的儿童。两名患者的右肾均有两条肾动脉。一名13岁男孩出现严重头痛、运动时下肢疼痛以及明显高血压(血压170/110)。主动脉造影显示其腹主动脉从肾上腺区域至髂总动脉分叉上方5厘米处狭窄70%。腹腔干、肠系膜上动脉和左肾动脉存在明显狭窄。右肾有两条肾动脉,上极动脉在其起始处狭窄。一名10岁女孩,已知患有高血压数年,其主动脉造影显示腹主动脉从肾上腺区域至髂总动脉分叉上方3厘米处狭窄70%。左肾动脉开口处受累。她的右肾也有两条肾动脉,右上极动脉在其起始处及血管中段狭窄。两例均采用聚四氟乙烯(PTFE)旁路移植术完成主动脉重建。第一例还包括腹腔干的补片血管成形术。两例均对右肾进行了自体肾移植。术中将右肾取出,进行冷灌注,重建两条肾动脉后移植至右髂血管。两例均将左肾动脉重新植入PTFE移植物。两名患者术后病程均顺利。13岁男孩通过二巯基丁二酸(DTPA)扫描显示自体移植肾下极部分存在肾缺血证据。他患有轻度高血压,通过抗高血压药物得以控制。10岁女孩DTPA扫描结果正常,血压正常。MAS是一种罕见且具有挑战性的先天性血管异常,可导致RVH。在存在双肾动脉的情况下,采用冷灌注和“体外”血管重建的自体肾移植技术可减少热缺血时间,并应能产生满意的效果。

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