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Nonoperative management of isolated celiac and superior mesenteric artery dissection: case report and review of the literature.

机译:孤立性腹腔和肠系膜上动脉夹层的非手术治疗:病例报告和文献复习。

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摘要

Isolated dissection of the origin of both celiac and superior mesenteric arteries is a rare vascular pathology with limited management guidelines. The presentation is generally nonspecific, most often manifesting with epigastric pain radiating to the back. A high diagnostic index of suspicion and stepwise management are essential for a successful outcome. This case report details the clinical course of a 57-year-male who presented with a 2-week history of epigastric discomfort with back pain and was found to have focal celiac artery dissection with aneurysmal dilation of 1.2 cm. His vital signs were stable, and the physical examination was unremarkable. At this time, he was placed on antiplatelet medication and was scheduled for endovascular repair of his celiac aneurysm with a covered stent graft. Two weeks later, recurrent abdominal pain prompted a repeat computed tomographic scan that revealed sequential superior mesenteric artery (SMA) dissection. The patient was admitted and anticoagulated. A complete workup ruled out underlying collagen vascular and autoimmune pathology. He remained stable, with significant symptomatic improvement. After 6 months, anticoagulation was discontinued and antiplatelet therapy was instituted for long-term management. Subsequent operative or endovascular intervention was not required. The patient was continuing to do well on his 18-month clinical follow-up. There are 71 cases of SMA and 12 cases of celiac artery dissection in the literature. This report outlines this rare presentation of isolated, proximal sequential celiac artery and SMA dissection. This case illustrates that conservative management may be warranted in uncomplicated, isolated visceral arterial dissection.
机译:仅对腹腔和肠系膜上动脉的起源进行解剖是一种罕见的血管病理,管理指南有限。表现通常是非特异性的,最常见的表现为上腹部疼痛辐射到背部。高度怀疑的诊断指数和分阶段处理对成功取得成功至关重要。该病例报告详细介绍了一位57岁男性的临床历程,该男性患者出现了2周的上腹不适并伴有背痛病史,并被发现患有乳糜泻,伴有1.2 cm的动脉瘤扩张。他的生命体征稳定,身体检查无异常。这时,他接受了抗血小板药物治疗,并计划使用覆盖的覆膜支架进行腹腔动脉瘤的血管内修复。两周后,复发性腹痛提示进行重复的计算机体层摄影扫描,显示顺序性肠系膜上动脉(SMA)解剖。该患者入院并进行了抗凝治疗。完整的检查排除了潜在的胶原血管和自身免疫病理。他保持稳定,症状明显改善。 6个月后,停止抗凝治疗,并开始长期治疗抗血小板治疗。不需要随后的手术或血管内干预。该患者在18个月的临床随访中一直表现良好。文献中有71例SMA和12例腹腔动脉夹层。该报告概述了这种罕见的孤立性,近端连续性腹腔动脉和SMA解剖的表现。这种情况说明,在简单,孤立的内脏动脉解剖中可能需要保守治疗。

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