Literature DB >> 20219272

[Hereditary multiple exostosis revealed by deep vein and arterial popliteal thrombosis].

S Toumi1, H Ghnaya, A Essid, A Braham, S Jerbi, K Mrad-Daly, C Laouani-Kechrid.   

Abstract

We report a 38-year-old man who presented successively a thrombosis of the right popliteal vein and the right popliteal artery, responsible of a painful edema of the leg. There was no known thrombophilic predisposing condition. Radiologic assessment, guided by clinical findings, evidenced bilateral femoral and tibial exostosis resulting in a diagnosis of hereditary multiples exostosis. Although anticoagulant treatment with unfractioned heparin was instituted, distal ischemia of the right lower limb developed. Resection of the compressive osteochondroma and an arterial femorotibial bypass venous graft were performed in addition to prolonged anticoagulant therapy. Outcome was eventually favorable. Hereditary multiple exostosis may be asymptomatic for long time. Compression of adjacent vascular structures by an osteochondroma is a rare and potentially serious complication. Copyright 2009. Published by Elsevier SAS.

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Year:  2010        PMID: 20219272     DOI: 10.1016/j.revmed.2009.03.359

Source DB:  PubMed          Journal:  Rev Med Interne        ISSN: 0248-8663            Impact factor:   0.728


  1 in total

1.  Small sharp exostosis tip in solitary osteochondroma causing intermittent knee pain due to pseudoaneurysm.

Authors:  Wiebke K Guder; Arne Streitbürger; Georg Gosheger; Michael Köhler; Dagmar Bachhuber; Marcel-Philipp Henrichs; Jendrik Hardes
Journal:  BMC Res Notes       Date:  2013-04-10
  1 in total

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