Neurology Unit, Department of Biomedical, Metabolic and Neural Science, University of Modena and Reggio Emilia, Modena, Italy.
Neurology Unit, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.
Neurol Sci. 2022 Jun;43(6):3979-3982. doi: 10.1007/s10072-022-06055-2. Epub 2022 Apr 7.
Antibodies against SOX1 (or anti-glial nuclear antibody, AGNA) are partially characterized onconeural antibodies, firstly described in association with small cell lung cancer (SCLC). Lambert-Eaton myasthenic syndrome is the most frequent paraneoplastic syndrome (PNS) found in patients with anti-SOX1-antibody positivity. Other associations are chronic axonal polyneuropathy, paraneoplastic limbic encephalitis, and paraneoplastic cerebellar degeneration.
We describe a case of Guillain-Barré syndrome (GBS) with classical demyelinating phenotype associated with a positivity for anti-SOX1-antibodies.
A therapy with intravenous immunoglobulin led to progressive clinical improvement. After 12 months, clinical and neurophysiological pictures showed complete recovery. A thorough paraneoplastic screening was negative for underlying tumors.
This is the first case of GBS associated with anti-SOX1-antibodies described in literature. Although the concept of paraneoplastic GBS is controversial, different cases have been reported and GBS is considered a non-classical paraneoplastic syndrome. Our case expands the anti-SOX1-antibody clinical spectrum with relevant implications for the clinical practice.
针对 SOX1 的抗体(或抗神经胶质核抗体,AGNA)是部分特征性的肿瘤相关抗体,最初与小细胞肺癌(SCLC)相关联被描述。Lambert-Eaton 肌无力综合征是抗 SOX1 抗体阳性患者中最常见的副肿瘤综合征(PNS)。其他相关疾病还有慢性轴索性多发性神经病、副肿瘤性边缘叶脑炎和副肿瘤性小脑变性。
我们描述了一例与抗 SOX1 抗体阳性相关的典型脱髓鞘表现的格林-巴利综合征(GBS)病例。
静脉注射免疫球蛋白治疗后,临床症状逐渐改善。12 个月后,临床和神经生理学表现完全恢复。彻底的副肿瘤筛查未发现潜在肿瘤。
这是文献中首例报道的与抗 SOX1 抗体相关的 GBS 病例。尽管副肿瘤性 GBS 的概念存在争议,但已有不同病例的报道,并且 GBS 被认为是非典型的副肿瘤综合征。我们的病例扩展了抗 SOX1 抗体的临床表现谱,对临床实践具有重要意义。