» Articles » PMID: 38471709

Identical Anatomy, Different Symptoms: a Comparative Case Study of Median Arcuate Ligament Syndrome in Monozygotic Twins

Overview
Journal BMJ Case Rep
Specialty General Medicine
Date 2024 Mar 12
PMID 38471709
Authors
Affiliations
Soon will be listed here.
Abstract

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.

References
1.
Horton K, Talamini M, Fishman E . Median arcuate ligament syndrome: evaluation with CT angiography. Radiographics. 2005; 25(5):1177-82. DOI: 10.1148/rg.255055001. View

2.
Arazinska A, Polguj M, Wojciechowski A, Trebinski L, Stefanczyk L . Median arcuate ligament syndrome: Predictor of ischemic complications?. Clin Anat. 2016; 29(8):1025-1030. DOI: 10.1002/ca.22773. View

3.
Kim E, Lamb K, Relles D, Moudgill N, DiMuzio P, Eisenberg J . Median Arcuate Ligament Syndrome-Review of This Rare Disease. JAMA Surg. 2016; 151(5):471-7. DOI: 10.1001/jamasurg.2016.0002. View

4.
Zaqqa M, Massumi A . Neurally mediated syncope. Tex Heart Inst J. 2000; 27(3):268-72. PMC: 101078. View

5.
Goodall R, Langridge B, Onida S, Ellis M, Lane T, Davies A . Median arcuate ligament syndrome. J Vasc Surg. 2019; 71(6):2170-2176. DOI: 10.1016/j.jvs.2019.11.012. View