Cytomegalovirus-Associated Parainfectious Miller Fisher Syndrome Without Anti-GQ1b Antibodies: A Case Report.

IF 0.7 Q4 CLINICAL NEUROLOGY
Alexandros Giannakis, Christos Papanicolaou, Spiridon Konitsiotis, Vasiliki Kostadima
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引用次数: 0

Abstract

Miller Fisher Syndrome (MFS) is a rare neurological disorder characterized by ataxia, areflexia, and ophthalmoplegia. It is considered a variant of Guillain-Barré syndrome (GBS). Infections frequently precede the onset of MFS. A 44-year-old patient was referred to our Neurology Department due to rapidly progressive bilateral limb ataxia, areflexia, and external ophthalmoplegia following acute tonsillitis with fever and oral mucosal lesions. Initial extensive diagnostic work-up, including immunoglobulin M (IgM) serum antibodies against cytomegalovirus (CMV), was negative. However, due to clinical suspicion, anti-CMV IgM was tested again and subsequently found to be positive. Interestingly, antibodies against Q1B ganglioside, which are specific for MFS, were also negative. Our patient gradually improved after intravenous immunoglobulin administration and symptomatic treatment. No underlying cause of immunocompromise was identified. This case underscores the importance of persistent testing for CMV antibodies in immunocompetent patients, even in rare cases of GBS like MFS, to ensure accurate diagnosis and optimize treatment plans.

无抗gq1b抗体的巨细胞病毒相关副感染性米勒费雪综合征1例报告
Miller Fisher综合征(MFS)是一种罕见的神经系统疾病,以共济失调、反射性松弛和眼麻痹为特征。它被认为是格林-巴- 综合征(GBS)的一种变体。感染通常先于MFS发病。一例44岁患者因急性扁桃体炎伴发热及口腔黏膜病变后出现双侧肢体共济失调、反射松弛及眼外麻痹而转介至我科。最初的广泛诊断检查,包括抗巨细胞病毒(CMV)的免疫球蛋白M (IgM)血清抗体,均为阴性。然而,由于临床怀疑,再次检测抗巨细胞病毒IgM,随后发现阳性。有趣的是,针对MFS特异性的Q1B神经节苷脂的抗体也呈阴性。患者经静脉注射免疫球蛋白及对症治疗后病情逐渐好转。没有确定免疫功能低下的潜在原因。该病例强调了在免疫功能正常的患者中持续检测巨细胞病毒抗体的重要性,即使是在罕见的GBS病例(如MFS)中,也要确保准确诊断和优化治疗计划。
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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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