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Ann Clin Neurophysiol > Volume 17(2); 2015 > Article
Ann Clin Neurophysiol. 2015; 17(2): 76-79.
Published online December 31, 2015.
doi: https://doi.org/10.14253/kjcn.2015.17.2.76
Recurrent Myelopathy in a Patient with Klippel-Trenaunay Syndrome
Yue Kyung Kim, Young In Eom, and In Soo Joo
Department of Neurology, Ajou University School of Medicine, Suwon, Korea
Corresponding Author: In Soo Joo ,Tel: +82-31-219-5172, Fax: +82-31-219-5178, Email: isjoo@ajou.ac.kr
Received November 4, 2014    Accepted July 8, 2015
Copyright 2015 by The Korean Society of Clinical Neurophysiology
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Klippel-Trenaunay syndrome (KTS) is a rare congenital malformation syndrome involving blood and lymph vessels, which is characterized by triad of cutaneous hemangioma, venous varicosities, and overgrowth of the affected limbs. Because vascular malformation in KTS can be located anywhere except the face and brain, the clinical presentation could be extremely variable. But there are only rare case reports that KTS is associated with spinal cord lesion. We report a case of recurrent myelopathy in a patient with KTS.
Key words: Myelopathy, Klippel-Trenaunay syndrome, Vascular malformation
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