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伴有腹腔干自发性夹层动脉瘤的正中弓状韧带综合征

Median Arcuate Ligament Syndrome (MALS) With a Spontaneous Dissecting Aneurysm of the Celiac Axis.

作者信息

Ward Ryan, Naidoo Devin, Shikhrakar Shreeja, Chaudhary Ranjit

机构信息

Radiology, Brown University, Providence, USA.

Radiology, Frank H. Netter MD School of Medicine, Quinnipiac University, North Haven, USA.

出版信息

Cureus. 2025 Jul 25;17(7):e88766. doi: 10.7759/cureus.88766. eCollection 2025 Jul.

Abstract

We present the fifth documented case, out of a total of four reported in the literature to date, of concurrent median arcuate ligament syndrome (MALS) and celiac artery dissecting aneurysm. A 42-year-old male arrived at the emergency department with acute-onset epigastric and left upper quadrant pain radiating to the left flank, accompanied by nausea without vomiting. Imaging with computed tomography angiography (CTA) confirmed a 1.3 cm dissecting aneurysm of the celiac axis with significant proximal stenosis caused by compression from the median arcuate ligament, consistent with MALS. The diagnosis was based solely on imaging findings; no specific clinical diagnostic criteria were applied. The patient was managed conservatively due to hemodynamic stability, absence of rupture, and stable aneurysmal size on serial imaging. He was discharged with antihypertensives and close outpatient follow-up, with a scheduled vascular surgery consultation in two weeks. We also discuss in this report the previously documented cases of the same or similar occurrences. Across these cases, treatment varied from conservative management to surgical intervention, often influenced by aneurysm stability and rupture risk. Our case adds to the limited literature on this rare presentation and highlights the potential for safe conservative management in select patients. It also underscores the need for diagnostic vigilance and follow-up protocols to better stratify management strategies in MALS-associated vascular complications. These cases emphasize the clinical importance of recognizing the rare coexistence of MALS and celiac artery dissection. Reporting such cases enhances awareness, facilitates early diagnosis, and may inform the development of standardized management approaches.

摘要

我们报告了第五例并发正中弓状韧带综合征(MALS)和腹腔动脉夹层动脉瘤的病例,这是迄今为止文献中总共报道的四例此类病例中的一例。一名42岁男性因急性发作的上腹部和左上腹疼痛放射至左胁腹而抵达急诊科,伴有恶心但无呕吐。计算机断层扫描血管造影(CTA)成像证实腹腔干有一个1.3厘米的夹层动脉瘤,伴有由正中弓状韧带压迫引起的明显近端狭窄,符合MALS。诊断仅基于影像学表现;未应用特定的临床诊断标准。由于血流动力学稳定、未破裂且系列成像显示动脉瘤大小稳定,该患者接受了保守治疗。他出院时服用了降压药并进行密切的门诊随访,计划在两周后进行血管外科会诊。我们还在本报告中讨论了先前记录的相同或类似情况的病例。在这些病例中,治疗方法从保守治疗到手术干预各不相同,这通常受动脉瘤稳定性和破裂风险的影响。我们的病例补充了关于这种罕见表现的有限文献,并强调了在特定患者中进行安全保守治疗的可能性。它还强调了对MALS相关血管并发症进行诊断警惕和随访方案以更好地分层管理策略的必要性。这些病例强调了认识到MALS和腹腔动脉夹层罕见共存的临床重要性。报告此类病例可提高认识、促进早期诊断,并可能为标准化管理方法的制定提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa4e/12296889/d2f6dafcf9a7/cureus-0017-00000088766-i01.jpg

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