Anti-SOX1 Antibody-Positive Paraneoplastic Syndrome Presenting with Subacute Cerebellar Degeneration and Lambert-Eaton Myasthenic Syndrome: A Case Report.

Q3 Medicine Acta neurologica Taiwanica Pub Date : 2021-06-01
Yung-Chun Cheng, Anna Chang, Wei-Chih Hsu
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引用次数: 0

Abstract

Purpose: Paraneoplastic neurological disorders associated with autoantibodies are rare diseases, causing abnormal manifestations in the central or peripheral nervous system separately or simultaneously. Early recognizing the occurrence of paraneoplastic syndrome can lead to prompt and effective management.

Case report: We presented a patient of subacute cerebellar degeneration with cachectic and bed-ridden status, who was proven to have positive SOX1 antibody. A coexisting Lambert-Eaton myasthenic syndrome was also documented by electrophysiological study.

Conclusion: Intensive and regular follow up for an occult malignancy is crucial in patients with SOX1 antibody. Coadministration of therapies for underlying malignancy and LEMS improve the functional disability.

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抗sox1抗体阳性副肿瘤综合征表现为亚急性小脑变性和兰伯特-伊顿肌无力综合征1例报告。
目的:伴随自身抗体的副肿瘤神经系统疾病是一种少见的疾病,可单独或同时在中枢或周围神经系统出现异常表现。早期认识到副肿瘤综合征的发生可以导致及时和有效的管理。病例报告:我们提出了一个亚急性小脑变性与恶病质和卧床状态,谁被证明有SOX1抗体阳性。电生理研究也证实了一种共存的兰伯特-伊顿肌无力综合征。结论:对隐匿性恶性肿瘤进行强化和定期随访对SOX1抗体患者至关重要。联合治疗潜在恶性肿瘤和LEMS可改善功能性残疾。
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来源期刊
Acta neurologica Taiwanica
Acta neurologica Taiwanica Medicine-Neurology (clinical)
CiteScore
1.30
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0.00%
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0
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