A Challenging Case of Miller Fisher Syndrome: The Importance of Clinical Recognition

Authors

  • Inês Almeida Serviço de Reumatologia, Unidade Local de Saúde Viseu Dão- Lafões, Viseu, Viseu, Portugal https://orcid.org/0009-0002-1825-209X
  • José Miguel Alves Serviço de Neurologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal https://orcid.org/0000-0003-2873-4121
  • Ana Morgadinho Serviço de Neurologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal
  • Inês Antunes Cunha Serviço de Neurologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal
  • Joana Andrade Serviço de Neurologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal https://orcid.org/0000-0001-5087-1355

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https://doi.org/10.60591/crspmi.42

Keywords:

Guillain-Barré syndrome, Miller Fisher Syndrome, Polyradiculoneuropathy

Abstract

Guillain-Barré syndrome (GBS) is an immune-mediated
polyradiculoneuropathy with several forms of presentation
being the sensory-motor the most frequent. Miller Fisher
syndrome (MFS) is a rare variant of GBS that is characterized by ophthalmoplegia, decreased osteotendinous reflexes and ataxia. We describe a twenty-five-years-old young man with subacute double vision, difficulty articulating words, muscle weakness and altered sensitivity. On neurological examination, he presented limitation of binocular abduction, peripheral facial dysparesis, dysphonia, dysarthria, dysphagia, decreased cervical strength, proximal-distal tetraparesis, hypo-reflexia and axial ataxia. Complementary diagnostic tests showed results within normal limits. He underwent five days of intravenous human Immunoglobulin and functional rehabilitation program, with excellent therapeutic
response and progressive improvement of neurological
deficits. In short, the clinical overlap between variants of GBS is a reality and, therefore, the early establishment of
the diagnosis and its therapeutic orientation are of vital importance in the prognosis of patients.

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Published

2024-06-24

How to Cite

Almeida, I., Alves, J. M., Morgadinho, A., Cunha, I. A., & Andrade, J. (2024). A Challenging Case of Miller Fisher Syndrome: The Importance of Clinical Recognition. SPMI Case Reports, 2(Edição Especial), 40–44. https://doi.org/10.60591/crspmi.42