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小儿内脏动脉闭塞性疾病:临床相关性及手术治疗

Pediatric splanchnic arterial occlusive disease: clinical relevance and operative treatment.

作者信息

Upchurch Gilbert R, Henke Peter K, Eagleton Matthew J, Grigoryants Vladimir, Sullivan Vita V, Wakefield Thomas W, Jacobs Lloyd A, Greenfield Lazar J, Stanley James C

机构信息

Section of Vascular Surgery, Department of Surgery, University of Michigan Hospital, 1500 E. Medical Center Drive, 2210THCC, Ann Arbor, MI 48109-0329, USA.

出版信息

J Vasc Surg. 2002 May;35(5):860-7. doi: 10.1067/mva.2002.123086.

Abstract

OBJECTIVE

Splanchnic arterial occlusive disease is rare in childhood. The purpose of this study was to review the clinical relevance and operative treatment of these lesions in a unique experience from a single institution.

METHODS

Seventeen children (11 boys and 6 girls) from 2 years to 17 years in age with critical narrowings of the celiac artery (CA) and superior mesenteric artery (SMA) underwent treatment at the University of Michigan from 1974 to 2000. Etiologic factors included embryologic fusion abnormalities of the fetal aortae during formation of the splanchnic arteries (n = 15), inflammatory aortoarteritis (n = 1), and radiation-induced arterial fibrosis (n = 1). Individual lesions included CA occlusions (n = 6) and stenoses (n = 7), SMA occlusions (n = 3) and stenoses (n = 11), and inferior mesenteric artery stenosis (n = 1). Fourteen children had abdominal aortic coarctations, and 15 had renal artery stenoses. Two patients had postprandial abdominal discomfort and food aversion, consistent with intestinal angina. Small stature affected five others, perhaps attributable to severe renovascular hypertension and failure to thrive. Ten children underwent intestinal revascularization, at the time of an aortoplasty or thoracoabdominal bypass for aortic coarctation (n = 7) or at the time of renal artery revascularization (n = 8). Primary splanchnic revascularization procedures included SMA-aortic implantation (n = 3), aorto-SMA and CA bypass with an internal iliac artery graft (n = 3) or a saphenous vein graft (n = 1), CA-aortic implantation at a stenotic SMA origin (n = 2), and CA and SMA intimectomy (n = 1). Secondary operations included SMA-aortic implantation (n = 2).

RESULTS

All 10 children who underwent splanchnic revascularization have thrived, gained weight, and are free of abdominal pain, with follow-up periods averaging 9 years. No intestinal ischemic manifestations occurred in the seven children who did not undergo operation.

CONCLUSION

Pediatric splanchnic arterial occlusive disease is a rare illness appropriately treated with operation in properly selected children.

摘要

目的

内脏动脉闭塞性疾病在儿童时期较为罕见。本研究的目的是通过单一机构的独特经验,回顾这些病变的临床相关性及手术治疗方法。

方法

1974年至2000年期间,17名年龄在2岁至17岁之间、患有腹腔干(CA)和肠系膜上动脉(SMA)严重狭窄的儿童在密歇根大学接受了治疗。病因包括内脏动脉形成过程中胎儿主动脉的胚胎融合异常(n = 15)、炎性主动脉动脉炎(n = 1)以及辐射诱导的动脉纤维化(n = 1)。具体病变包括CA闭塞(n = 6)和狭窄(n = 7)、SMA闭塞(n = 3)和狭窄(n = 11)以及肠系膜下动脉狭窄(n = 1)。14名儿童患有腹主动脉缩窄,15名患有肾动脉狭窄。两名患者有餐后腹部不适和厌食物,符合肠绞痛表现。身材矮小影响了另外五名儿童,这可能归因于严重的肾血管性高血压和发育不良。10名儿童在进行主动脉缩窄的主动脉成形术或胸腹旁路手术时(n = 7)或肾动脉血运重建时(n = 8)接受了肠道血运重建。原发性内脏血运重建手术包括SMA - 主动脉植入(n = 3)、使用髂内动脉移植物(n = 3)或大隐静脉移植物(n = 1)进行主动脉 - SMA和CA旁路、在狭窄的SMA起始处进行CA - 主动脉植入(n = 2)以及CA和SMA内膜切除术(n = 1)。二次手术包括SMA - 主动脉植入(n = 2)。

结果

所有10名接受内脏血运重建的儿童均茁壮成长、体重增加且无腹痛,平均随访期为9年。7名未接受手术的儿童未出现肠道缺血表现。

结论

小儿内脏动脉闭塞性疾病是一种罕见疾病,在适当选择的儿童中通过手术治疗是合适的。

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