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A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis
INTRODUCTION: We present here a case of West Nile Virus (WNV) encephalitis that initially presented with diabetic ketoacidosis and rhabdomyolysis. CASE PRESENTATION: A 35-year-old male with no past medical history presented to the emergency department complaining of polydipsia, generalized weakness,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378900/ https://www.ncbi.nlm.nih.gov/pubmed/30815360 http://dx.doi.org/10.1016/j.idcr.2019.e00505 |
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author | Burden, Zachary Fasen, Madeline Judkins, Benjamin L. Isache, Carmen |
author_facet | Burden, Zachary Fasen, Madeline Judkins, Benjamin L. Isache, Carmen |
author_sort | Burden, Zachary |
collection | PubMed |
description | INTRODUCTION: We present here a case of West Nile Virus (WNV) encephalitis that initially presented with diabetic ketoacidosis and rhabdomyolysis. CASE PRESENTATION: A 35-year-old male with no past medical history presented to the emergency department complaining of polydipsia, generalized weakness, lightheadedness, and visual disturbances of one week duration. He was found to be in diabetic ketoacidosis. His hemoglobin A1c was 11%. The patient was appropriately treated for diabetic ketoacidosis and it resolved on hospital day 1. On hospital day 2, the patient developed a fever of 101.6 °F and his mental status became severely altered. He developed auditory and visual hallucinations. IgM and IgG antibodies to West Nile Virus were positive in the cerebral spinal fluid (CSF). The patient's creatine kinase level rose to 118,400 U/L during his hospitalization and eventually returned to baseline. The patient made a full recovery with no residual neurologic deficits after an 11 day hospital course. DISCUSSION: In this patient, neuroinvasive WNV was confirmed with positive CSF IgM. The patient’s newly diagnosed diabetes likely contributed to his susceptibility to neuroinvasive disease. Furthermore, WNV encephalitis in a background of DKA has not been previously described in the literature and this case demonstrates WNV neuroinvasive disease should be in the differential diagnosis for patients presenting with unexplained neurological symptoms. CONCLUSION: Diagnosis of neuroinvasive WNV is imperative to stop unnecessary therapies, limit further diagnostic evaluation, help predict patient outcomes, direct public health prevention measures, and further provide investigations into the clinical conditions that define the spectrum of WNV disease. |
format | Online Article Text |
id | pubmed-6378900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-63789002019-02-27 A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis Burden, Zachary Fasen, Madeline Judkins, Benjamin L. Isache, Carmen IDCases Article INTRODUCTION: We present here a case of West Nile Virus (WNV) encephalitis that initially presented with diabetic ketoacidosis and rhabdomyolysis. CASE PRESENTATION: A 35-year-old male with no past medical history presented to the emergency department complaining of polydipsia, generalized weakness, lightheadedness, and visual disturbances of one week duration. He was found to be in diabetic ketoacidosis. His hemoglobin A1c was 11%. The patient was appropriately treated for diabetic ketoacidosis and it resolved on hospital day 1. On hospital day 2, the patient developed a fever of 101.6 °F and his mental status became severely altered. He developed auditory and visual hallucinations. IgM and IgG antibodies to West Nile Virus were positive in the cerebral spinal fluid (CSF). The patient's creatine kinase level rose to 118,400 U/L during his hospitalization and eventually returned to baseline. The patient made a full recovery with no residual neurologic deficits after an 11 day hospital course. DISCUSSION: In this patient, neuroinvasive WNV was confirmed with positive CSF IgM. The patient’s newly diagnosed diabetes likely contributed to his susceptibility to neuroinvasive disease. Furthermore, WNV encephalitis in a background of DKA has not been previously described in the literature and this case demonstrates WNV neuroinvasive disease should be in the differential diagnosis for patients presenting with unexplained neurological symptoms. CONCLUSION: Diagnosis of neuroinvasive WNV is imperative to stop unnecessary therapies, limit further diagnostic evaluation, help predict patient outcomes, direct public health prevention measures, and further provide investigations into the clinical conditions that define the spectrum of WNV disease. Elsevier 2019-02-13 /pmc/articles/PMC6378900/ /pubmed/30815360 http://dx.doi.org/10.1016/j.idcr.2019.e00505 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Burden, Zachary Fasen, Madeline Judkins, Benjamin L. Isache, Carmen A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
title | A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
title_full | A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
title_fullStr | A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
title_full_unstemmed | A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
title_short | A case of West Nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
title_sort | case of west nile virus encephalitis accompanied by diabetic ketoacidosis and rhabdomyolysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378900/ https://www.ncbi.nlm.nih.gov/pubmed/30815360 http://dx.doi.org/10.1016/j.idcr.2019.e00505 |
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