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Korean J Spine Search

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DOI: https://doi.org/10.14245/kjs.2011.8.2.125   
Solitary Hemangioblastoma at the Filum Terminale: A Case Report and Review of Literature.
Jung Hoon Lee, Jin Uk Kim, Sung Suk Paeng, Jee Soo Jang, Sang Ho Lee
1Department of Neurosurgery, Seoul Wooridul Hospital, Seoul, Korea.
2Department of Orthopaedic Surgery, Seoul Wooridul Hospital, Seoul, Korea. ultralex@wooridul.co.kr
3Department of Pathology, Seoul Wooridul Hospital, Seoul, Korea.
Abstract
Spinal hemangioblastomas at the filum terminale are rare. Only a few reports present immunohistopathological features of spinal hemangioblastomas. A 55-year-old woman presented with sustained low back pain and intermittent numbness in both lower extremities. She already had a decompressive surgery for a left L5-S1 extraforaminal lesion 7 months ago. Her incidental mass lesion had been slightly enlarged for 7 months and concordant symptoms had also been prolonged. Her tumor was removed en bloc with a unilateral hemilaminotomy and bilateral decompression technique. The patient's symptoms improved immediately after the surgery. In immunohistochemical stains, the stromal cells were positive for inhibin-alpha, neuron specific enolase (NSE), and the endothelial cells were positive for CD31, CD34, and factor VIII related antigen in confirming the diagnosis of hemangioblastoma. We report a rare case of intradural extramedullary spinal hemangioblastoma at the filum terminale. Complete en bloc resection was achieved with no morbidity. The immunohistopathological staining include inhibin-alpha confirmed an accurate diagnosis of the hemangioblastoma distinguishing from other vascular tumors.
Keywords: Spinal hemangioblastoma;Filum terminale;Immunohistopathological stain


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