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Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature
RATIONALE: Miller Fisher syndrome (MFS) is a rare variant of Guillain-Barre syndrome, classically diagnosed based on the clinical triad of ataxia, areflexia, and ophthalmoplegia. MFS is usually preceded by viral infections and febrile illness; however, only a few cases have been reported after vacci...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276158/ https://www.ncbi.nlm.nih.gov/pubmed/35608434 http://dx.doi.org/10.1097/MD.0000000000029333 |
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author | Siddiqi, Ahsun Rizwan Khan, Tehrim Tahir, Muhammad Junaid Asghar, Muhammad Sohaib Islam, Md. Saiful Yousaf, Zohaib |
author_facet | Siddiqi, Ahsun Rizwan Khan, Tehrim Tahir, Muhammad Junaid Asghar, Muhammad Sohaib Islam, Md. Saiful Yousaf, Zohaib |
author_sort | Siddiqi, Ahsun Rizwan |
collection | PubMed |
description | RATIONALE: Miller Fisher syndrome (MFS) is a rare variant of Guillain-Barre syndrome, classically diagnosed based on the clinical triad of ataxia, areflexia, and ophthalmoplegia. MFS is usually preceded by viral infections and febrile illness; however, only a few cases have been reported after vaccinations. PATIENT CONCERNS: A 53-year-old hypertensive male presented with a 2-day history of progressive ascending paralysis of the lower limbs along with diplopia and ataxia, 8 days after the first dose of the Sinovac–Coronavac coronavirus disease 2019 (COVID-19) vaccination, with no prior history of any predisposing infections or triggers. DIAGNOSES: Physical examination showed moderate motor and sensory loss with areflexia in the lower limbs bilaterally. Routine blood investigations and radiological investigations were unremarkable. Cerebrospinal fluid analysis showed albuminocytologic dissociation and nerve conduction studies revealed prolonged latencies with reduced conduction velocities. The diagnosis of MFS was established based on the findings of physical examination, cerebrospinal fluid analysis, and nerve conduction studies. INTERVENTIONS: A management plan was devised based on intravenous immunoglobulins, pregabalin, and physiotherapy. However, due to certain socioeconomic factors, the patient was managed conservatively with regular physiotherapy sessions. OUTCOMES: Follow-up after 6 weeks showed remarkable improvement, with complete resolution of symptoms 10 weeks after the discharge. LESSONS: This case suggests that MFS is a rare adverse effect after COVID-19 vaccination and additional research is required to substantiate a temporal association. Further studies are needed to understand the pathophysiology behind such complications to enhance the safety of COVID-19 vaccinations in the future. |
format | Online Article Text |
id | pubmed-9276158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-92761582022-07-13 Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature Siddiqi, Ahsun Rizwan Khan, Tehrim Tahir, Muhammad Junaid Asghar, Muhammad Sohaib Islam, Md. Saiful Yousaf, Zohaib Medicine (Baltimore) 5300 RATIONALE: Miller Fisher syndrome (MFS) is a rare variant of Guillain-Barre syndrome, classically diagnosed based on the clinical triad of ataxia, areflexia, and ophthalmoplegia. MFS is usually preceded by viral infections and febrile illness; however, only a few cases have been reported after vaccinations. PATIENT CONCERNS: A 53-year-old hypertensive male presented with a 2-day history of progressive ascending paralysis of the lower limbs along with diplopia and ataxia, 8 days after the first dose of the Sinovac–Coronavac coronavirus disease 2019 (COVID-19) vaccination, with no prior history of any predisposing infections or triggers. DIAGNOSES: Physical examination showed moderate motor and sensory loss with areflexia in the lower limbs bilaterally. Routine blood investigations and radiological investigations were unremarkable. Cerebrospinal fluid analysis showed albuminocytologic dissociation and nerve conduction studies revealed prolonged latencies with reduced conduction velocities. The diagnosis of MFS was established based on the findings of physical examination, cerebrospinal fluid analysis, and nerve conduction studies. INTERVENTIONS: A management plan was devised based on intravenous immunoglobulins, pregabalin, and physiotherapy. However, due to certain socioeconomic factors, the patient was managed conservatively with regular physiotherapy sessions. OUTCOMES: Follow-up after 6 weeks showed remarkable improvement, with complete resolution of symptoms 10 weeks after the discharge. LESSONS: This case suggests that MFS is a rare adverse effect after COVID-19 vaccination and additional research is required to substantiate a temporal association. Further studies are needed to understand the pathophysiology behind such complications to enhance the safety of COVID-19 vaccinations in the future. Lippincott Williams & Wilkins 2022-05-27 /pmc/articles/PMC9276158/ /pubmed/35608434 http://dx.doi.org/10.1097/MD.0000000000029333 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections. |
spellingShingle | 5300 Siddiqi, Ahsun Rizwan Khan, Tehrim Tahir, Muhammad Junaid Asghar, Muhammad Sohaib Islam, Md. Saiful Yousaf, Zohaib Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature |
title | Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature |
title_full | Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature |
title_fullStr | Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature |
title_full_unstemmed | Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature |
title_short | Miller Fisher syndrome after COVID-19 vaccination: Case report and review of literature |
title_sort | miller fisher syndrome after covid-19 vaccination: case report and review of literature |
topic | 5300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276158/ https://www.ncbi.nlm.nih.gov/pubmed/35608434 http://dx.doi.org/10.1097/MD.0000000000029333 |
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