Anti-SOX1 Antibodies in a 3-Year-old Girl, Post-Varicella.

Child neurology open Pub Date : 2023-09-21 eCollection Date: 2023-01-01 DOI:10.1177/2329048X231200613
Aline Wijnand, Helene Verhelst
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Abstract

Anti-SRY-related HMG-box gene 1 (SOX1) antibodies were initially described in adults with paraneoplastic neurological disorders, where they are considered high-risk onconeural autoantibodies. Only two pediatric cases of anti-SOX1 antibodies have been reported: a 17-year-old adolescent presenting with paraneoplastic limbic encephalitis due to Hodgkin lymphoma and a 12-year-old girl presenting with non-paraneoplastic encephalitis. We present a unique case of anti-SOX1 antibodies in a 3-year-old girl, post-varicella infection. Initially, she presented with ataxia and dysmetria, with subsequent reports from parents of urinary incontinence and significant behavior changes. Additionally, reflexes in the lower limbs were absent. Anti-SOX1 antibodies tested positive in both serum and cerebrospinal fluid. Oncological screening at presentation and a seven-month follow-up showed no malignancies. The patient exhibited favorable clinical progress without requiring treatment. At the seven-month follow-up, serum antibodies tested negative. This case report broadens the known clinical spectrum, being the first description of post-varicella anti-SOX1 antibodies.

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水痘后3岁女孩体内的抗SOX1抗体。
抗SRY相关的HMG-box基因1(SOX1)抗体最初被描述为患有副肿瘤性神经系统疾病的成年人,在那里它们被认为是高风险的肿瘤神经自身抗体。只有两例抗SOX1抗体的儿科病例被报道:一名17岁的青少年因霍奇金淋巴瘤而出现副肿瘤性边缘脑炎,另一名12岁的女孩出现非副肿瘤性脑炎。我们报告了一例3岁女孩水痘后感染的抗SOX1抗体的独特病例。起初,她表现为共济失调和视障,随后父母报告她有尿失禁和明显的行为变化。此外,下肢没有反射。血清和脑脊液中的抗SOX1抗体均呈阳性。肿瘤筛查和七个月的随访显示没有恶性肿瘤。患者在无需治疗的情况下表现出良好的临床进展。在7个月的随访中,血清抗体检测呈阴性。该病例报告拓宽了已知的临床范围,是水痘后抗SOX1抗体的首次描述。
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