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Int J Angiol 2002; 11(1): 7-8
DOI: 10.1007/s00547-001-0045-9
Original Articles

© Georg Thieme Verlag KG Stuttgart · New York

Klippel-Trenaunay syndrome: A rare cause of severe headache

Abraham J. Sorom, David Driscoll, Anthony Stanson
  • Department of Pediatric and Adolescent Medicine, Division of Pediatric Cardiology and the Department of Vascular and Interventional Radiology, Mayo Clinic and Mayo Medical School, Rochester, Minnesota
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Publikationsdatum:
25. April 2011 (online)

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Abstract

Klippel-Trenaunay Syndrome (KTS) is a rare condition characterized by the triad of capillary malformations (port-wine stains), venous malformations, and soft tissue and/or bony hypertrophy. Many patients with KTS have pain of the affected area of the body. We report a unique KTS patient with multiple intraosseous calvarial venous malformations producing severe chronic headaches.

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