Idiopathic Spinal Epidural Lipomatosis: A Case Report
Spinal epidural lipomatosis (SEDL) is a rare disorder and is usually associated with long-term steroid administration. SEDL develops in some patients in the absence of elevated steroid levels. Limited information on idiopathic SEDL comes predominantly from isolated case reports. We report a case of...
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Published in | Orthopedics & Traumatology Vol. 58; no. 3; pp. 411 - 414 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | Japanese English |
Published |
West-Japanese Society of Orthopedics & Traumatology
25.09.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Spinal epidural lipomatosis (SEDL) is a rare disorder and is usually associated with long-term steroid administration. SEDL develops in some patients in the absence of elevated steroid levels. Limited information on idiopathic SEDL comes predominantly from isolated case reports. We report a case of SEDL in a 70-year-old man presented with intermitted claudication. He was evaluated by myelography, computed tomography, and magnetic resonance imaging. Surgical treatment was performed by laminectomies and fat debulking. After surgery, he showed gradual improvement in symptoms and neurological conditions. |
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ISSN: | 0037-1033 1349-4333 |
DOI: | 10.5035/nishiseisai.58.411 |