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[腘动脉压迫综合征]

[Popliteal artery entrapment syndrome].

作者信息

Sepa G, Dzsinich C, Szabó A, Nemes A, Szeberin Z

机构信息

Semmelweis Orvostudományi Egyetem Er- és Szívsebészeti Klinika.

出版信息

Magy Seb. 2000 Feb;53(1):17-20.

PMID:11299586
Abstract

Popliteal Artery Entrapment Syndrome (PAES) is an uncommon congenital anomaly. It arises due to compression of the popliteal artery by tendomuscular structures often combined with an anomalous position of the artery. Mostly young men are suffering of this disease. There are four common variations of this anomaly. We report on a 14 year old patient who had an acute 24 hours duration right leg ischemia caused by PAES. Using a posterior approach to the popliteal artery, following division of the accessory slip of gastrocnemius muscle we performed an arteriotomy and a floating thrombus was removed. The artery was reconstructed by direct continuous suture. One year postoperatively the boy has no complaints, peripheral pulse is palpable.

摘要

腘动脉压迫综合征(PAES)是一种罕见的先天性异常。它是由于肌腱肌肉结构对腘动脉的压迫,常伴有动脉位置异常而引起的。该病多见于年轻男性。这种异常有四种常见类型。我们报告一例14岁患者,因PAES导致急性右下肢缺血24小时。采用腘动脉后入路,在切断腓肠肌副腱后,我们进行了动脉切开术并清除了漂浮血栓。动脉通过直接连续缝合进行重建。术后一年,该男孩无不适,可触及外周脉搏。

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