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Miller-Fisher Syndrome: A Case Report and Review of the Literature
INTRODUCTION: Neurological complaints are a common presenting symptom seen by the emergency physician. However, the Miller-Fisher variant of Guillain-Barré syndrome is a rare cause of neurological complaints seen in the emergency department. CASE REPORT: A 26-year-old male presented with dysphonia a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676776/ https://www.ncbi.nlm.nih.gov/pubmed/33217300 http://dx.doi.org/10.5811/cpcem.2020.7.48507 |
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author | Truong, Justina Conley, Jeff Ashurst, John |
author_facet | Truong, Justina Conley, Jeff Ashurst, John |
author_sort | Truong, Justina |
collection | PubMed |
description | INTRODUCTION: Neurological complaints are a common presenting symptom seen by the emergency physician. However, the Miller-Fisher variant of Guillain-Barré syndrome is a rare cause of neurological complaints seen in the emergency department. CASE REPORT: A 26-year-old male presented with dysphonia and bilateral hand and feet paresthesia after a recent diarrheal illness. Examination revealed the absence of tricep, brachioradialis, patellar and Achilles tendon reflexes bilaterally, and difficulty with phonation. Lumbar puncture revealed the presence of anti-GQ1b antibodies, and the patient was diagnosed with Miller-Fisher variant of Guillain-Barré. DISCUSSION: Miller-Fisher syndrome is an acute, autoimmune response that typically follows either an upper respiratory or diarrheal illness. Typically associated with dysfunction of cranial nerves three, four, and six, Miller-Fisher syndrome may present with facial paralysis, opthalmoplegia, arefexia, or ataxia. Lumbar puncture with the presence of anti-GQ1b antibodies is indicative. Treatment could include supportive respiratory care, intravenous immunoglobulin therapy, or plasmapheresis. CONCLUSION: Miller-Fisher syndrome is a rare form of Guillain-Barré syndrome that the emergency provider should include in the differential when faced with a patient with cranial nerve dysfunction. |
format | Online Article Text |
id | pubmed-7676776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-76767762020-11-24 Miller-Fisher Syndrome: A Case Report and Review of the Literature Truong, Justina Conley, Jeff Ashurst, John Clin Pract Cases Emerg Med ACOEP Case Report INTRODUCTION: Neurological complaints are a common presenting symptom seen by the emergency physician. However, the Miller-Fisher variant of Guillain-Barré syndrome is a rare cause of neurological complaints seen in the emergency department. CASE REPORT: A 26-year-old male presented with dysphonia and bilateral hand and feet paresthesia after a recent diarrheal illness. Examination revealed the absence of tricep, brachioradialis, patellar and Achilles tendon reflexes bilaterally, and difficulty with phonation. Lumbar puncture revealed the presence of anti-GQ1b antibodies, and the patient was diagnosed with Miller-Fisher variant of Guillain-Barré. DISCUSSION: Miller-Fisher syndrome is an acute, autoimmune response that typically follows either an upper respiratory or diarrheal illness. Typically associated with dysfunction of cranial nerves three, four, and six, Miller-Fisher syndrome may present with facial paralysis, opthalmoplegia, arefexia, or ataxia. Lumbar puncture with the presence of anti-GQ1b antibodies is indicative. Treatment could include supportive respiratory care, intravenous immunoglobulin therapy, or plasmapheresis. CONCLUSION: Miller-Fisher syndrome is a rare form of Guillain-Barré syndrome that the emergency provider should include in the differential when faced with a patient with cranial nerve dysfunction. University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2020-09-09 /pmc/articles/PMC7676776/ /pubmed/33217300 http://dx.doi.org/10.5811/cpcem.2020.7.48507 Text en Copyright: © 2020 Truong et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) License. See: http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | ACOEP Case Report Truong, Justina Conley, Jeff Ashurst, John Miller-Fisher Syndrome: A Case Report and Review of the Literature |
title | Miller-Fisher Syndrome: A Case Report and Review of the Literature |
title_full | Miller-Fisher Syndrome: A Case Report and Review of the Literature |
title_fullStr | Miller-Fisher Syndrome: A Case Report and Review of the Literature |
title_full_unstemmed | Miller-Fisher Syndrome: A Case Report and Review of the Literature |
title_short | Miller-Fisher Syndrome: A Case Report and Review of the Literature |
title_sort | miller-fisher syndrome: a case report and review of the literature |
topic | ACOEP Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676776/ https://www.ncbi.nlm.nih.gov/pubmed/33217300 http://dx.doi.org/10.5811/cpcem.2020.7.48507 |
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