兄弟姐妹中的腘动脉压迫综合征

Popliteal Artery Entrapment Syndrome in Siblings.

作者信息

Orimoto Yuki, Mitsuoka Hiroki, Imaeda Yusuke, Arima Takahiro, Maruyama Yuki, Yamada Tetsuya, Ishibashi Hiroyuki

机构信息

Department of Vascular Surgery, Aichi Medical University, Nagakute, Aichi, Japan.

出版信息

Ann Vasc Dis. 2020 Jun 25;13(2):198-201. doi: 10.3400/avd.cr.20-00031.

DOI:10.3400/avd.cr.20-00031

PMID:32595801

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7315233/

Abstract

Popliteal artery entrapment syndrome (PAES) is a rare disease. We treated siblings with this disease. An 18-year-old male consulted our hospital for intermittent claudication of the left lower limb. Contrast-enhanced computed tomography led to a diagnosis of type II PAES. After transection of the medial head of the gastrocnemius muscle, popliteal artery bypass was performed. His younger brother (6 years younger) was also diagnosed with type II PAES, and similar surgery was performed at the age of 19. These cases suggested the involvement of genetic factors in PAES in addition to embryological factors.

摘要

腘动脉压迫综合征（PAES）是一种罕见疾病。我们治疗了患有这种疾病的兄弟姐妹。一名18岁男性因左下肢间歇性跛行前来我院就诊。增强计算机断层扫描诊断为II型PAES。在切断腓肠肌内侧头后，进行了腘动脉搭桥手术。他6岁的弟弟也被诊断为II型PAES，并在19岁时进行了类似手术。这些病例表明，除胚胎学因素外，遗传因素也与PAES有关。