无腹腔动脉压迫静态图像表现的正中弓状韧带综合征:可能存在纯神经源性亚型。

Atsushi Okita, Nobuji Yokoyama
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引用次数: 0

摘要

症状性正中弓状韧带综合征(MALS)被认为是一种排除性诊断,其诊断标准尚无共识。我们提出的情况下,一个39岁的妇女,谁提出了持续的上腹部疼痛。计算机断层扫描未显示腹腔外动脉(CA)狭窄。超声检查显示,吸气和呼气位置CA的收缩血流速度峰值分别为1.13 m/sec和2.16 m/sec。最大吸气与最大呼气主动脉与CA夹角差约50°。只有患者的身体表现提示MALS,因为超声检查结果显示正常流动,没有压缩通过腹腔轴。患者行腹腔镜下正中弓韧带(MAL)切开术,术后症状消失。肌萎缩侧索硬化症的病理生理机制尚不清楚,本病例提示肌萎缩侧索硬化症可能存在神经源性亚型,其中肌萎缩侧索硬化症压迫乳糜丛,但不压迫CA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Median Arcuate Ligament Syndrome Without Static Image Findings of Celiac Artery Compression: The Potential Existence of a Pure Neurogenic Subtype.

Symptomatic median arcuate ligament syndrome (MALS) is considered to be a diagnosis of exclusion, and there is no consensus about its diagnostic criteria. We present the case of a 39-year-old woman, who presented with persistent epigastric pain. A computed tomography scan did not show external celiac artery (CA) stenosis. Ultrasonography showed that the peak systolic blood flow velocity of the CA in inspiration and expiration position was 1.13 m/sec and 2.16 m/sec, respectively. The difference in the angle between the aorta and CA between maximum inspiration and maximum expiration was >50°. Only the patient's physical findings were suggestive of MALS, as the ultrasonographic findings demonstrated normal flow without compression through the celiac axis. The patient underwent laparoscopic division of the median arcuate ligament (MAL), and her symptoms disappeared postoperatively. The pathophysiology of MALS remains unclear, and our case suggests the potential existence of a neurogenic subtype in which MAL compresses the celiac plexus, but not the CA.

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