Identical anatomy, different symptoms: a comparative case study of median arcuate ligament syndrome in monozygotic twins

被引:0
|
作者
Anthony, Lakmali [1 ]
Gillies, Madeline [2 ]
Bayat, Iman [3 ]
机构
[1] Vasc Surg, Northern Hlth NCHER, Epping, Vic, Australia
[2] Western Hlth, Footscray, Vic, Australia
[3] Northern Hosp, Vasc Surg, Epping, Vic, Australia
关键词
Gastrointestinal system; General surgery; Vascular surgery;
D O I
10.1136/bcr-2024-259684
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Median arcuate ligament syndrome (MALS) is a rare clinical entity arising from the extrinsic compression of the coeliac axis by the median arcuate ligament. In this report, we detail a unique presentation involving monozygotic twins, both of whom demonstrated anatomical extrinsic compression of the coeliac axis by the median arcuate ligament. Intriguingly, only one twin manifested clinical symptoms consistent with MALS, despite comparable anatomical compression of the coeliac axis observed in both. This case highlights the potential interplay of a genetic or anatomical predisposition to coeliac axis compression and secondary, possibly environmental, factors that lead to the development of clinical symptoms. In this report, we explore various determinants potentially influencing symptomatology in MALS and advocate for the publication of similar case studies to further elucidate this rare condition.
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页数:4
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