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Sudden onset of paraplegia caused by hemorrhagic spinal epidural angiolipoma. A case report

机译:出血性脊髓硬膜外血管脂肪瘤引起的截瘫突然发作。病例报告

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摘要

Spinal epidural angiolipoma is a rare benign tumor containing vascular and mature adipose elements. A slow progressive clinical course was mostly presented and rarely a fluctuating course during pregnancy. The authors report the original case of spontaneous spinal epidural bleeding resulting from thoracic epidural angiolipoma who presented with hyperacute onset of paraplegia, simulating an extradural hematoma. The patient was admitted with sudden non-traumatic hyperacute paraplegia during a prolonged walk. Neurologic examination showed sensory loss below T6 and bladder disturbances. Spinal MRI revealed a non-enhanced heterogeneous thoracic epidural lesion, extending from T2 to T3. A bilateral T2–T4 laminectomy was performed to achieve resection of a lipomatous tumor containing area of spontaneous hemorrhage. The postoperative course was uneventful with complete neurologic recovery. Histologic examination revealed the tumor as an angiolipoma. Because the prognosis after rapid surgical management of this lesion is favorable, the diagnosis of spinal angiolipoma with bleeding should be considered in the differential diagnosis of hyperacute spinal cord compression.
机译:脊髓硬膜外血管脂肪瘤是一种罕见的良性肿瘤,含有血管和成熟的脂肪成分。缓慢进展的临床过程主要表现在怀孕期间,很少出现波动。作者报告了由胸膜硬膜外血管脂肪瘤引起的自发性脊柱硬膜外出血的原始病例,其表现为截瘫的超急性发作,模拟了硬膜外血肿。该患者在长时间的行走过程中突然出现非创伤性超急性截瘫。神经系统检查显示低于T6的感觉丧失和膀胱障碍。脊柱MRI显示未增强的异质胸膜硬膜外病变,从T2延伸至T3。进行了双侧T2-T4椎板切除术,以切除包含自发性出血区域的脂肪瘤。术后过程平稳,神经系统完全恢复。组织学检查显示该肿瘤为血管脂肪瘤。由于对该病进行快速外科治疗后的预后良好,因此在对超急性脊髓压迫进行鉴别诊断时,应考虑诊断伴有出血的脊髓血管脂瘤。

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