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Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease?
West Nile virus (WNV) is a mosquito-borne RNA Flavivirus which emerged in North America in 1999. Most patients present with a febrile illness but a few develop WNV neuroinvasive disease. Myopathy is an uncommon manifestation. We describe a case of a 42-year-old male from Los Angeles who presented wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826924/ https://www.ncbi.nlm.nih.gov/pubmed/27119037 http://dx.doi.org/10.1155/2016/5395249 |
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author | Kiran, Aneeta R. Lau, Richard A. Wu, Kim M. Wong, Andrew L. Clements, Philip J. Heinze, Emil R. |
author_facet | Kiran, Aneeta R. Lau, Richard A. Wu, Kim M. Wong, Andrew L. Clements, Philip J. Heinze, Emil R. |
author_sort | Kiran, Aneeta R. |
collection | PubMed |
description | West Nile virus (WNV) is a mosquito-borne RNA Flavivirus which emerged in North America in 1999. Most patients present with a febrile illness but a few develop WNV neuroinvasive disease. Myopathy is an uncommon manifestation. We describe a case of a 42-year-old male from Los Angeles who presented with 8 days of fever and muscle pain. Initial physical exam was normal except for 4/5 muscle strength testing in his extremity proximal muscles. Laboratory revealed a creatine kinase of 45,000 and a urinalysis with large blood but no red blood cells, suggesting rhabdomyolysis. The patient's condition declined despite aggressive supportive care and hydration, and on hospital day #6 he developed severe altered mental status and progressed to complete right arm paralysis and 2/5 muscle strength in bilateral legs. EMG/NCS showed sensorimotor axonal polyneuropathy and the cerebrospinal fluid was positive for IgM and IgG WNV antibodies. The patient was diagnosed with WNV neuroinvasive disease, poliomyelitis (and encephalitis) type with myopathy/muscle involvement. He was treated supportively and his muscle and neurologic disease gradually improved. At 12-month follow-up his muscle enzymes had normalized and his weakness had improved to 5/5 strength in bilateral legs and 3/5 strength in the right arm. |
format | Online Article Text |
id | pubmed-4826924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48269242016-04-26 Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? Kiran, Aneeta R. Lau, Richard A. Wu, Kim M. Wong, Andrew L. Clements, Philip J. Heinze, Emil R. Case Rep Rheumatol Case Report West Nile virus (WNV) is a mosquito-borne RNA Flavivirus which emerged in North America in 1999. Most patients present with a febrile illness but a few develop WNV neuroinvasive disease. Myopathy is an uncommon manifestation. We describe a case of a 42-year-old male from Los Angeles who presented with 8 days of fever and muscle pain. Initial physical exam was normal except for 4/5 muscle strength testing in his extremity proximal muscles. Laboratory revealed a creatine kinase of 45,000 and a urinalysis with large blood but no red blood cells, suggesting rhabdomyolysis. The patient's condition declined despite aggressive supportive care and hydration, and on hospital day #6 he developed severe altered mental status and progressed to complete right arm paralysis and 2/5 muscle strength in bilateral legs. EMG/NCS showed sensorimotor axonal polyneuropathy and the cerebrospinal fluid was positive for IgM and IgG WNV antibodies. The patient was diagnosed with WNV neuroinvasive disease, poliomyelitis (and encephalitis) type with myopathy/muscle involvement. He was treated supportively and his muscle and neurologic disease gradually improved. At 12-month follow-up his muscle enzymes had normalized and his weakness had improved to 5/5 strength in bilateral legs and 3/5 strength in the right arm. Hindawi Publishing Corporation 2016 2016-03-28 /pmc/articles/PMC4826924/ /pubmed/27119037 http://dx.doi.org/10.1155/2016/5395249 Text en Copyright © 2016 Aneeta R. Kiran et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kiran, Aneeta R. Lau, Richard A. Wu, Kim M. Wong, Andrew L. Clements, Philip J. Heinze, Emil R. Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? |
title | Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? |
title_full | Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? |
title_fullStr | Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? |
title_full_unstemmed | Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? |
title_short | Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease? |
title_sort | fever, myositis, and paralysis: is this inflammatory myopathy or neuroinvasive disease? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826924/ https://www.ncbi.nlm.nih.gov/pubmed/27119037 http://dx.doi.org/10.1155/2016/5395249 |
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