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I.はじめに
脊髄動静脈奇形のnidusは胸腰髄レベルに多く,仙髄レベルでは非常に稀である9,12).
今回著者らは,直腸肛門機能障害にて発症し,L2レベルまで上行する脊髄症状を呈したが,実際にはnidusはS1レベルの硬膜外にあった動静脈奇形の1例を経験した,この動静脈奇形は,両側内腸骨動脈より導入血管を受けていた.本例の症状発現機序に考察を加え報告する.
A rare case of a spinal epidural AVM fed by bilateral internal iliac arteries is reported. The patient was a 50 years old female with symptoms of slowly progressive paraparesis and sensory disturb-ance below L-2 associated with sphincter disorders. Myelography disclosed a serpiginous filling defect at the lumbar region. Selective internal iliac arterio-grams disclosed an AVM fed by bilateral lateral sacral arteries. The nidus was excised totally, then a gradual improvement of those symptoms followed.
Reviewing the literature, only 9 cases of spinal AVM of this type have been reported.
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