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Miller-Fisher syndrome after first dose of Oxford/AstraZeneca coronavirus disease 2019 vaccine: a case report.
Pirola, Fernanda Junqueira Cesar; Santos, Bruno Antônio Müzel; Sapienza, Gabriela Feres; Cetrangolo, Lucas Yuri; Geranutti, Caio Henrique Wthen Gambacorta; de Aguiar, Paulo Henrique Pires.
  • Pirola FJC; Department of Medical Science, Medical School, Catholic Pontifical University of Sao Paulo, Sorocaba, Brazil. fernandajcp@gmail.com.
  • Santos BAM; Department of Medical Science, Medical School, Catholic Pontifical University of Sao Paulo, Sorocaba, Brazil.
  • Sapienza GF; Department of Medical Science, Medical School, Catholic Pontifical University of Sao Paulo, Sorocaba, Brazil.
  • Cetrangolo LY; Department of Neurology, Division of Clinical Medicine, Catholic Pontifical University of Sao Paulo, Sorocaba, Brazil.
  • Geranutti CHWG; Department of Neurology, Division of Clinical Medicine, Catholic Pontifical University of Sao Paulo, Sorocaba, Brazil.
  • de Aguiar PHP; Department of Neurology, Division of Neurology, Catholic Pontifical University of Sao Paulo, Sorocaba, Brazil.
J Med Case Rep ; 16(1): 437, 2022 Nov 16.
Article in English | MEDLINE | ID: covidwho-2113828
ABSTRACT

INTRODUCTION:

Miller-Fisher Syndrome (MFS) is a variant of Guillain-Barré syndrome (GBS), an acute immune-mediated neuropathy, which manifests as a rapidly evolving areflex motor paralysis. This syndrome presents as a classic triad ophthalmoplegia, areflexia, and ataxia. MFS is usually benign and self-limited. CASE REPORT A Caucasian patient was admitted to our hospital with the flu, loss of bilateral strength in the lower limbs and upper limbs and sudden-onset ataxia 7 days after receiving a first dose of the Oxford/AstraZeneca COVID-19 vaccine. On neurological examination, the patient had Glasgow Coma Scale score of 15, with absence of meningeal signs; negative Babinski sign; grade 2 strength in the lower limbs and grade 4 strength in the upper limbs; axial and appendicular cerebellar ataxia; and peripheral facial diparesis predominantly on the right, without conjugate gaze deviation. Cerebrospinal fluid (CSF) was collected on admission, and analysis revealed albuminocytological dissociation with CSF protein of 148.9 mg/dL; leukocytes, 1; chlorine, 122; glucose, 65 mg/mL; red cells, 2; and non-reactive venereal disease research laboratory test result. The COVID-19 IgG/IgM rapid immunological test was negative. Electroneuromyography revealed a recent moderate-grade and primarily sensory and motor demyelinating polyneuropathy with associated proximal motor block. DISCUSSION AND

CONCLUSION:

Miller-Fisher Syndrome may be related to events other than infections prior to neuropathy, as in the case reported here. The patient presented strong correlations with findings for MFS reported in the literature, such as the clinical condition, the results of electroneuromyography, and results of the CSF analysis typical for MFS. When treatment was provided as proposed in the literature, the disease evolved with improvement. Ultimately, the diagnosis of incomplete MFS was made, including acute ataxic neuropathy (without ophthalmoplegia).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ophthalmoplegia / Miller Fisher Syndrome / COVID-19 Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid / Vaccines / Variants Limits: Humans Language: English Journal: J Med Case Rep Year: 2022 Document Type: Article Affiliation country: S13256-022-03592-4

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Ophthalmoplegia / Miller Fisher Syndrome / COVID-19 Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid / Vaccines / Variants Limits: Humans Language: English Journal: J Med Case Rep Year: 2022 Document Type: Article Affiliation country: S13256-022-03592-4