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Case Reports
Spontaneous dissection of the popliteal artery in a young man. A rare cause of the blue toe syndrome.
- C F A Kügler, M Poser, F Mosel, S Ruehm, and G Rudofsky.
- Department and Clinic of Angiology, University of Essen, Essen, Germany. c.kuegler@hgz-bb.de
- Int Angiol. 2006 Mar 1; 25 (1): 93-7.
AbstractSpontaneous arterial dissection in peripheral arteries of the extremities is an extremely rare event. We report a case of a spontaneous dissection of a nonaneurysmal popliteal artery in an otherwise healthy 36-year-old man that came to clinical attention as an acute blue toe syndrome. The diagnosis was primarily made by high-resolution duplex ultrasound that revealed a dissection flap (length: 15.5 mm; thickness: 0.4 mm) together with the partially thrombosed false lumen at the dorsal wall of the left popliteal artery (degree of local diameter reduction: 56%). Further work-up by means of contrast-enhanced MR-A and conventional DSA confirmed a moderate stenosis of the popliteal artery compatible with focal dissection and excluded other causes such as popliteal artery entrapment syndrome. Under full-dose intravenous anticoagulation with unfractionated heparin that was switched to oral anticoagulation with vitamin K antagonists (target INR: 2-3) and conservative management of the blue toe the patient made a gradual, but eventually complete clinical recovery over 8 weeks.
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