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Japanese

Spinal Arteriovenous Malformations in Klippel-Trenaunay-Weber Syndrome: Case report En-Chow TAN 1 , Takuji TAKAGI 2 , Hajime NAGAI 1 1Department of Neurosurgery, Nagoya City University Medical School 2Department of Neurosurgery, Nagoya City Higashi General Hospital Keyword: Klippel-Trénaunay-Weber Syndrome , Spinal arteriovenous malformation pp.877-881
Published Date 1990/9/10
DOI https://doi.org/10.11477/mf.1436900142
  • Abstract
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A 19-year-old man was admitted with the chief com-plaint of a sudden onset of thoracic pain and paraple-gia. His right lower limb had progressively enlarged since he was 3 months old. Transient paraparesis had occurred recurrently since the age of 3. Physical ex-amination on admission revealed that there were multi-ple warts on his face, trunk and right extremities. The right lower limb was thicker and longer than the left one, and the temperature was 1°C higher in the right side.


Copyright © 1990, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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