Spinal Hemangioblastoma of Cauda Equina Origin Not Associated With Von Hippel-Lindau Syndrome -Case Report-
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- KUNIHIRO Noritsugu
- Department of Neurosurgery, Osaka City University Graduate School of Medicine
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- TAKAMI Toshihiro
- Department of Neurosurgery, Osaka City University Graduate School of Medicine
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- YAMAGATA Toru
- Department of Neurosurgery, Osaka City University Graduate School of Medicine
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- TSUYUGUCHI Naohiro
- Department of Neurosurgery, Osaka City University Graduate School of Medicine
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- OHATA Kenji
- Department of Neurosurgery, Osaka City University Graduate School of Medicine
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- タイトル別名
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- —Case Report—
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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
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- Neurologia medico-chirurgica
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Neurologia medico-chirurgica 51 (10), 732-735, 2011
一般社団法人 日本脳神経外科学会
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詳細情報 詳細情報について
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- CRID
- 1390282680033026304
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- NII論文ID
- 10029479363
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- NII書誌ID
- AN00358613
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- ISSN
- 13498029
- 04708105
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- 使用不可