An Abnormal Presentation of a Popliteal Artery Mass and a Unique Cause of Claudication.

IF 0.6 Q4 ORTHOPEDICS
Case Reports in Orthopedics Pub Date : 2026-04-21 eCollection Date: 2026-01-01 DOI:10.1155/cro/9960715
Jamil Haddad, Majed Alzahabi, Saif L Juma, Nicholas David Cominos, Shariff K Bishai
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引用次数: 0

Abstract

Multiple hereditary exostosis (MHE) is a rare autosomal-dominant disorder marked by multiple osteochondromas arising from the metaphyses of long bones. Parameniscal cysts, often linked to meniscal tears, can also expand and compress nearby vessels, posing a potential vascular risk. We present a 28-year-old male with MHE and a parameniscal cyst causing popliteal artery compression. The patient's intermittent claudication resolved completely following surgical cyst decompression and meniscal repair. This case report highlights the importance of considering vascular compression in patients with MHE who present with lower extremity symptoms.

腘动脉肿块的异常表现和跛行的独特原因。
多发性遗传性外生骨病(MHE)是一种罕见的常染色体显性疾病,其特征是长骨的骨软骨瘤。腹膜旁囊肿通常与半月板撕裂有关,也会扩张和压迫附近的血管,造成潜在的血管风险。我们报告一位28岁的男性MHE合并腹膜旁囊肿导致腘动脉受压。经手术囊肿减压及半月板修复后,患者的间歇性跛行完全消失。本病例报告强调了在MHE患者出现下肢症状时考虑血管压迫的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
14 weeks
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