| Literature DB >> 32595801 |
Yuki Orimoto1, Hiroki Mitsuoka1, Yusuke Imaeda1, Takahiro Arima1, Yuki Maruyama1, Tetsuya Yamada1, Hiroyuki Ishibashi1.
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.Entities:
Keywords: familial occurrence; hereditary disorder; popliteal artery entrapment syndrome
Year: 2020 PMID: 32595801 PMCID: PMC7315233 DOI: 10.3400/avd.cr.20-00031
Source DB: PubMed Journal: Ann Vasc Dis ISSN: 1881-641X