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多发性内脏动脉动脉瘤合并正中弓状韧带综合征的治疗:病例研究及文献复习。

Combined Treatment of Multiple Splanchnic Artery Aneurysms Secondary to Median Arcuate Ligament Syndrome: A Case Study and Review of the Literature.

机构信息

Department of General, Endocrine and Vascular Surgery, Medical University of Warsaw, Warsaw, Poland.

II Division of Radiology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Am J Case Rep. 2020 Aug 11;21:e926074. doi: 10.12659/AJCR.926074.

Abstract

BACKGROUND Median arcuate ligament syndrome (MALS) is a rare and often misdiagnosed condition affecting about 0.4% of the population, typically ages 20-50 years old, and more frequently females. Caused by the compression of the celiac artery and adjacent nervous structures by the median arcuate ligament, it is typically manifested by postprandial abdominal pain, nausea or vomiting, and loss of weight. This condition also results in compensatory increased blood flow in peripancreatic arcades, facilitating formation of true aneurysms of the visceral vessels. CASE REPORT A 45-year-old woman with hypertension and left inferior renal pole cysts was referred to our department due to chronic, recurrent postprandial abdominal pains, nausea, and weight loss of approximately 15 kg in 1 year. A computed tomography (CT) scan demonstrated complete occlusion of the celiac trunk, significant stenosis of the superior mesenteric artery, and multiple aneurysms up to 17 mm in collateral circulatory vessels. Surgical decompression of the median arcuate ligament was performed and venous bypass was implanted between the aorta and the common hepatic artery, resulting in restoration of proper blood in the visceral circulation. Subsequently, 2 endovascular embolizations of visceral aneurysms were successfully performed. In the 48-month follow-up period, there was resolution of symptoms and no aneurysm formation was observed. CONCLUSIONS Endovascular methods should be the treatment of choice in patients with splanchnic artery aneurysms. However, in patients with multiple aneurysms secondary to MALS, arterial reconstruction may be considered prior to performing an endovascular procedure to restore physiological blood flow in the visceral circulation.

摘要

背景

中位弓状韧带综合征(MALS)是一种罕见且常被误诊的疾病,影响约 0.4%的人群,典型发病年龄为 20-50 岁,女性更为多见。由于中位弓状韧带压迫腹腔动脉和邻近的神经结构,常表现为餐后腹痛、恶心或呕吐以及体重减轻。这种情况还会导致胰周环流的代偿性血流增加,促进内脏血管真性动脉瘤的形成。

病例报告

一名 45 岁女性,患有高血压和左肾下极囊肿,因慢性、复发性餐后腹痛、恶心和体重减轻约 15 公斤,于 1 年前就诊于我院。计算机断层扫描(CT)显示腹腔干完全闭塞,肠系膜上动脉严重狭窄,侧支循环血管中存在多个 17 毫米的动脉瘤。行中位弓状韧带松解术,在主动脉和肝总动脉之间植入静脉旁路,恢复内脏循环的适当血流。随后成功进行了 2 次内脏动脉瘤的血管内栓塞术。在 48 个月的随访期间,症状缓解,未观察到动脉瘤形成。

结论

对于内脏动脉动脉瘤患者,血管内方法应是首选治疗方法。然而,对于 MALS 引起的多发动脉瘤患者,在进行血管内操作之前,可能需要考虑动脉重建以恢复内脏循环的生理血流。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/418f/7440745/e3a6e1352693/amjcaserep-21-e926074-g001.jpg

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