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内脏动脉孤立性自发性夹层

Isolated spontaneous dissection of the splanchnic arteries.

作者信息

Takayama Toshio, Miyata Tetsuro, Shirakawa Motoaki, Nagawa Hirokazu

机构信息

Division of Vascular Surgery, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

J Vasc Surg. 2008 Aug;48(2):329-33. doi: 10.1016/j.jvs.2008.03.002. Epub 2008 May 23.

Abstract

OBJECTIVES

Isolated dissection of a splanchnic artery, including the celiac artery, superior mesenteric artery (SMA), and inferior mesenteric artery, and their branches, is a relatively rare condition. This study was conducted to define the characteristics of patients with splanchnic artery dissection and the clinical course of isolated splanchnic artery dissection.

METHODS

The records of 19 patients were reviewed to survey demographic data, the location of dissection, symptoms, diagnostic modalities, treatment, and long-term outcome.

RESULTS

The locations of dissection were the superior mesenteric artery (SMA) in 11 patients, celiac artery in 3, both celiac artery and SMA in 2, and common hepatic artery, celiac artery to splenic artery, and celiac artery to proper hepatic artery in 1 each. In all but one with systemic sclerosis and Sjögren syndrome, the underlying cause of dissection was unclear. There were 12 asymptomatic and seven symptomatic patients. All cases were diagnosed by computed tomography. Surgical treatment was performed in one patient with a large aneurysm of the common hepatic artery, and the remaining 18 patients were followed-up conservatively. The mean follow-up duration was 20.9 +/- 25.4 months (range, 2-116 months). No expansion or progression of the false lumen was observed in these patients.

CONCLUSION

Patients with spontaneous dissection of the splanchnic arteries are often asymptomatic, and in this series, none developed significant end organ ischemia. Most patients with this rare condition can be managed expectantly with clinical follow-up including computed tomography imaging to assess aneurysm formation.

摘要

目的

内脏动脉孤立性夹层,包括腹腔干动脉、肠系膜上动脉(SMA)和肠系膜下动脉及其分支,是一种相对罕见的病症。本研究旨在明确内脏动脉夹层患者的特征以及孤立性内脏动脉夹层的临床病程。

方法

回顾19例患者的记录,以调查人口统计学数据、夹层位置、症状、诊断方式、治疗及长期预后。

结果

夹层位置为肠系膜上动脉(SMA)11例、腹腔干动脉3例、腹腔干动脉和肠系膜上动脉均受累2例、肝总动脉、腹腔干动脉至脾动脉、腹腔干动脉至肝固有动脉各1例。除1例患有系统性硬化症和干燥综合征外,其余患者夹层的潜在病因均不明确。无症状患者12例,有症状患者7例。所有病例均通过计算机断层扫描确诊。1例肝总动脉巨大动脉瘤患者接受了手术治疗,其余18例患者接受保守随访。平均随访时间为20.9±25.4个月(范围2 - 116个月)。这些患者中未观察到假腔扩张或进展。

结论

内脏动脉自发性夹层患者通常无症状,在本系列研究中,无一例发生严重的终末器官缺血。大多数患有这种罕见病症的患者可通过临床随访(包括计算机断层扫描成像以评估动脉瘤形成)进行观察处理。

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