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Atypical presentation of extraspinal neurofibroma presenting with acute-onset monoparesis and Horner's syndrome: Case report and review of literature

机译:急性发病单一性和霍尔综合征呈上升神经纤维瘤的非典型介绍:案例报告和文学综述

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The clinical presentation of spinal or extraspinal neurofibroma is radiculopathy or myelopathy, pain, and motor weakness. Extraspinal neurofibroma presenting with acute-onset monoparesis and Horner's syndrome is very rare. We report the case of a 55-year-old female who presented with acute-onset monoparesis of the left upper limb along with left-side drooping of the eyelid. Imaging revealed C6–D2 extraspinal solitary mass lesion lateral to spinous process with bleed without intraspinal component. The patient underwent an anterior cervical approach and excision of the tumor. Final biopsy report was a neurofibroma. At 3-year follow-up, she recovered from motor weakness, and Horner's syndrome subsided. Extraspinal neurofibroma can present with acute bleed, and surgical outcome is superior in early intervention.
机译:脊柱或附着神经纤维瘤的临床介绍是放射性的或肌钙病,疼痛和电动机的弱点。患有急性发作的术语和角氏综合征的海拔神经纤维瘤非常罕见。我们举报了55岁女性的案例,左上肢的急性发作,以及眼睑的左侧下垂。成像揭示了C6-D2中间孤立物质病变横向于棘突的伴随而不具有脊柱组分。患者接受了颈部宫颈近处和肿瘤的切除。最终的活组织检查报告是一种神经纤维瘤。她在3年的随访中,她从电机弱点恢复过来,霍尔综合征消退。隐藏性神经纤维瘤可以呈急性出血,并且早期干预的外科结果优于优异。

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