Shah Sarth, Patel Niket, Spitzer Laurence
Radiology, Drexel University College of Medicine, Philadelphia, USA.
Radiology, University of Pennsylvania, Philadelphia, USA.
Cureus. 2025 Apr 29;17(4):e83177. doi: 10.7759/cureus.83177. eCollection 2025 Apr.
Median arcuate ligament syndrome (MALS) is a rare vascular disorder caused by the compression of the celiac artery by the median arcuate ligament, leading to symptoms such as postprandial abdominal pain, weight loss, and nausea. While MALS typically affects the celiac artery, it can also result in downstream vascular complications, including dilatation of the superior mesenteric artery (SMA) to compensate for impaired blood flow, which can compress the left renal vein and cause nutcracker syndrome (NCS). This cascade may lead to secondary varicocele, characterized by dilatation of the pampiniform venous plexus. We present a case of a 21-year-old male with abdominal pain, nausea, weight loss, and heaviness in his scrotum who was found to have a large left-sided varicocele on physical examination. Diagnostic imaging revealed MALS with celiac artery compression, SMA dilatation, and compression of the left renal vein, indicative of NCS. These findings suggest a unique vascular interplay, where SMA dilatation caused by collateral flow compensating for celiac artery obstruction contributed to secondary varicocele formation. The patient was informed of his diagnosis but ultimately declined surgical treatment. This case underscores the importance of thorough diagnostic imaging and clinical evaluation in patients with rare overlapping vascular compression syndromes. It highlights the potential for a hemodynamic relationship between MALS, SMA dilatation, and NCS, contributing to the development of a varicocele. Further research is warranted to explore shared mechanisms and refine management strategies for such rare vascular presentations.
正中弓状韧带综合征(MALS)是一种罕见的血管疾病,由正中弓状韧带压迫腹腔干动脉引起,导致餐后腹痛、体重减轻和恶心等症状。虽然MALS通常影响腹腔干动脉,但它也可导致下游血管并发症,包括肠系膜上动脉(SMA)扩张以补偿血流受损,这可能压迫左肾静脉并导致胡桃夹综合征(NCS)。这种连锁反应可能导致继发性精索静脉曲张,其特征为蔓状静脉丛扩张。我们报告一例21岁男性,有腹痛、恶心、体重减轻和阴囊坠胀感,体格检查发现左侧有大的精索静脉曲张。诊断性影像学检查显示存在MALS伴腹腔干动脉受压、SMA扩张和左肾静脉受压,提示NCS。这些发现提示了一种独特的血管相互作用,即由侧支血流补偿腹腔干动脉阻塞引起的SMA扩张导致了继发性精索静脉曲张的形成。患者被告知诊断结果,但最终拒绝手术治疗。该病例强调了对罕见的重叠血管压迫综合征患者进行全面诊断性影像学检查和临床评估的重要性。它突出了MALS、SMA扩张和NCS之间血流动力学关系的可能性,这有助于精索静脉曲张的发展。有必要进行进一步研究以探索共同机制并完善对此类罕见血管表现的管理策略。