Spinal Hemangioblastoma of Cauda Equina Origin Not Associated With Von Hippel-Lindau Syndrome -Case Report-

  • KUNIHIRO Noritsugu
    Department of Neurosurgery, Osaka City University Graduate School of Medicine
  • TAKAMI Toshihiro
    Department of Neurosurgery, Osaka City University Graduate School of Medicine
  • YAMAGATA Toru
    Department of Neurosurgery, Osaka City University Graduate School of Medicine
  • TSUYUGUCHI Naohiro
    Department of Neurosurgery, Osaka City University Graduate School of Medicine
  • OHATA Kenji
    Department of Neurosurgery, Osaka City University Graduate School of Medicine

書誌事項

タイトル別名
  • —Case Report—

この論文をさがす

抄録

A 50-year-old male presented with a rare case of hemangioblastoma of cauda equina origin, without clinical signs of von Hippel-Lindau syndrome, manifesting as pain radiating from the back to the left thigh. Magnetic resonance imaging before surgery revealed an intradural spinal tumor at the L3-L4 levels with serpentine flow voids of tortuous and convoluted vessels, which appeared to be continuous with the left L5 nerve root. Surgical removal of the tumor was successfully accomplished via the posterior unilateral approach, and the histological diagnosis was hemangioblastoma. Clinical symptoms resolved dramatically after surgery, although the patient developed mild dysesthesia of the left L5 area early after surgery which was gradually improved late after surgery.<br>

収録刊行物

被引用文献 (2)*注記

もっと見る

参考文献 (38)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ