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Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature
BACKGROUND: Although dengue viral infections have emerged as one of the most important mosquito-borne diseases, neurological manifestations of dengue infections are uncommon. Guillain–Barré syndrome and Miller Fisher syndrome have been reported to occur as immune-mediated complications following den...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495497/ https://www.ncbi.nlm.nih.gov/pubmed/31043165 http://dx.doi.org/10.1186/s13256-019-2066-z |
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author | de Silva, Nipun Lakshitha Weeratunga, Praveen Umapathi, Thirugnanam Malavige, Neelika Chang, Thashi |
author_facet | de Silva, Nipun Lakshitha Weeratunga, Praveen Umapathi, Thirugnanam Malavige, Neelika Chang, Thashi |
author_sort | de Silva, Nipun Lakshitha |
collection | PubMed |
description | BACKGROUND: Although dengue viral infections have emerged as one of the most important mosquito-borne diseases, neurological manifestations of dengue infections are uncommon. Guillain–Barré syndrome and Miller Fisher syndrome have been reported to occur as immune-mediated complications following dengue infection. We report the case of a patient who developed Miller Fisher syndrome during the acute phase of dengue fever suggesting that Miller Fisher syndrome may arise as a result of direct neurotropism of the dengue virus. CASE PRESENTATION: A 70-year-old Sri Lankan man with well-controlled diabetes mellitus and hypertension presented with fever of 3 days’ duration, drooping of eyelids, dysarthria, and unsteady gait. He developed bilateral asymmetric partial ptosis, complete external ophthalmoplegia, bilateral palatal palsy, unilateral tongue weakness, ataxia, and areflexia from the second day of illness. He did not have limb weakness. He had evidence of acute dengue infection including progressive thrombocytopenia and leukopenia, positive dengue non-structural protein 1 antigen, dengue immunoglobulin M antibodies, and polymerase chain reaction detection of dengue virus genome in serum. Magnetic resonance imaging of his brain and cerebrospinal fluid analysis were normal. Polymerase chain reaction for dengue virus and immunoglobulin M antibodies in cerebrospinal fluid were negative. Nerve conduction studies showed axonal neuropathy. Antibodies (immunoglobulin G, immunoglobulin M, and immunoglobulin A) against GQ1b and GT1a were negative. He was treated with intravenously administered immunoglobulins and a recommended fluid regimen for dengue fever. He made a complete recovery from dengue fever in 7 days and Miller Fisher syndrome in 20 days. CONCLUSIONS: This case report highlights the rare occurrence of Miller Fisher syndrome during the acute phase of dengue fever. Neurological manifestations may occur as a consequence of direct neurotropism of dengue virus. |
format | Online Article Text |
id | pubmed-6495497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64954972019-05-08 Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature de Silva, Nipun Lakshitha Weeratunga, Praveen Umapathi, Thirugnanam Malavige, Neelika Chang, Thashi J Med Case Rep Case Report BACKGROUND: Although dengue viral infections have emerged as one of the most important mosquito-borne diseases, neurological manifestations of dengue infections are uncommon. Guillain–Barré syndrome and Miller Fisher syndrome have been reported to occur as immune-mediated complications following dengue infection. We report the case of a patient who developed Miller Fisher syndrome during the acute phase of dengue fever suggesting that Miller Fisher syndrome may arise as a result of direct neurotropism of the dengue virus. CASE PRESENTATION: A 70-year-old Sri Lankan man with well-controlled diabetes mellitus and hypertension presented with fever of 3 days’ duration, drooping of eyelids, dysarthria, and unsteady gait. He developed bilateral asymmetric partial ptosis, complete external ophthalmoplegia, bilateral palatal palsy, unilateral tongue weakness, ataxia, and areflexia from the second day of illness. He did not have limb weakness. He had evidence of acute dengue infection including progressive thrombocytopenia and leukopenia, positive dengue non-structural protein 1 antigen, dengue immunoglobulin M antibodies, and polymerase chain reaction detection of dengue virus genome in serum. Magnetic resonance imaging of his brain and cerebrospinal fluid analysis were normal. Polymerase chain reaction for dengue virus and immunoglobulin M antibodies in cerebrospinal fluid were negative. Nerve conduction studies showed axonal neuropathy. Antibodies (immunoglobulin G, immunoglobulin M, and immunoglobulin A) against GQ1b and GT1a were negative. He was treated with intravenously administered immunoglobulins and a recommended fluid regimen for dengue fever. He made a complete recovery from dengue fever in 7 days and Miller Fisher syndrome in 20 days. CONCLUSIONS: This case report highlights the rare occurrence of Miller Fisher syndrome during the acute phase of dengue fever. Neurological manifestations may occur as a consequence of direct neurotropism of dengue virus. BioMed Central 2019-05-02 /pmc/articles/PMC6495497/ /pubmed/31043165 http://dx.doi.org/10.1186/s13256-019-2066-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report de Silva, Nipun Lakshitha Weeratunga, Praveen Umapathi, Thirugnanam Malavige, Neelika Chang, Thashi Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
title | Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
title_full | Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
title_fullStr | Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
title_full_unstemmed | Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
title_short | Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
title_sort | miller fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495497/ https://www.ncbi.nlm.nih.gov/pubmed/31043165 http://dx.doi.org/10.1186/s13256-019-2066-z |
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