West Nile Encephalitis Differential Diagnoses

  • Author: Burke A Cunha, MD; Chief Editor: Michael Stuart Bronze, MD   more...
 
Updated: Jun 17, 2011
 
 

Diagnostic Considerations

The most important infection to exclude in the differential is herpes simplex virus type 1 (HSV-1) encephalitis, because it is the only treatable viral encephalitis. HSV-1 encephalitis is suggested by temporal lobe abnormalities on electroencephalograms and later on computed tomography (CT) and magnetic resonance imaging (MRI) scans.

Early in the course of HSV-1 encephalitis, cerebrospinal fluid (CSF) may initially show a polymorphonuclear predominance, frequently has red blood cells (RBCs), and may be associated with a decreased CSF glucose level in contrast to the CSF in WNE, which does not have any of these features.

HSV-1 encephalitis is the most common cause of non–arthropod-borne (nonseasonal) encephalitis in the United States. HSV-1 infection usually manifests as encephalitis, uncommonly as meningoencephalitis, or rarely as aseptic meningitis. Differential diagnoses of meningoencephalitis, including the HSV-1 type, are listed in the chart below.

Differential diagnoses of meningoencephalitis. Differential diagnoses of meningoencephalitis.

Encephalopathy due to systemic illnesses

Encephalopathy is a feature of many systemic illnesses that the clinician should consider in patients presenting with encephalitis. Most of these patients have extra-CNS findings that suggest the underlying disease process. Common disorders with CNS manifestations that may mimic West Nile encephalitis (WNE) include subacute bacterial endocarditis, Legionnaires disease, Rocky Mountain spotted fever, Epstein-Barr virus infectious mononucleosis, human herpesvirus type 6 infection, and systemic lupus erythematosus cerebritis.

Other arthropod-borne viral encephalitides

The clinical presentation of WNE is not dissimilar from other causes of arthropod-borne viral encephalitis (eg, Japanese equine encephalitis, St. Louis encephalitis), including mental confusion, stupor, or coma. However, the clinical presentation of arthropod-borne viral encephalitis is characterized by rapid onset and severe headache. Arthropod-borne viral encephalitis has some distinctive features that indicate a prospective clinical diagnosis (as seen

in the charts below).

Common encephalitis associations. Common encephalitis associations. Clinical features of arboviral encephalitis. Clinical features of arboviral encephalitis.

Enteroviral aseptic meningitis

The most common cause of aseptic meningitis encountered during the summer months is enteroviral meningitis. Enteroviral aseptic meningitis is most commonly due to coxsackieviruses but may also be due to enterocytopathogenic human orphan virus or nonparalytic strains of poliovirus. Enteroviral meningitis may occur after water exposure in swimming pools, lakes, streams, or oceans, as well as after contact with infected individuals.

Acute enteroviral CNS infections usually manifest as aseptic meningitis, uncommonly as meningoencephalitis, or, rarely, as encephalitis. Nonexudative pharyngitis, maculopapular extremity rash, loose stools, and even diarrhea often accompany enteroviral aseptic meningitis, which provides clues to its presence.

Excluding enterovirus 71, enteroviral meningitis is not accompanied by paralysis or prolonged and/or profound lymphopenia.

Nonsteroidal anti-inflammatory drugs

In patients who present with aseptic meningitis, consider drug-induced aseptic meningitis, most commonly due to nonsteroidal anti-inflammatory drugs (NSAIDs). A patient presenting with aseptic meningitis with no predisposing risk factors may have recently been taking NSAIDs or may be currently taking NSAIDs. Discontinue NSAIDs if the patient is taking them.

Differential Diagnoses

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Contributor Information and Disclosures
Author

Burke A Cunha, MD  Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital

Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Specialty Editor Board

Wesley W Emmons, MD, FACP  Assistant Professor, Department of Medicine, Thomas Jefferson University; Consulting Staff, Infectious Diseases Section, Department of Internal Medicine, Christiana Care, Newark, DE

Wesley W Emmons, MD, FACP is a member of the following medical societies: American College of Physicians, American Medical Association, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, and International AIDS Society

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

John L Brusch, MD, FACP  Assistant Professor of Medicine, Harvard Medical School; Consulting Staff, Department of Medicine and Infectious Disease Service, Cambridge Health Alliance

John L Brusch, MD, FACP is a member of the following medical societies: American College of Physicians and Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Chief Editor

Michael Stuart Bronze, MD  Professor, Stewart G Wolf Chair in Internal Medicine, Department of Medicine, University of Oklahoma Health Science Center

Michael Stuart Bronze, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Physician Executives, American College of Physicians, American College of Physicians-American Society of Internal Medicine, American Federation for Clinical Research, American Medical Association, American Society for Microbiology, Association of Professors of Medicine, Association of Program Directors in Internal Medicine, Infectious Diseases Society of America, Oklahoma State Medical Association, and Southern Society for Clinical Investigation

Disclosure: Nothing to disclose.

References
  1. Cunha BA. Alexander the Great and West Nile virus encephalitis. Emerg Infect Dis. Jul 2004;10(7):1328-9; author reply 1332-3. [Medline].

  2. Oldach D, Benitez RM, Mackowiak PA. Alexander the Great and West Nile virus encephalitis. Emerg Infect Dis. Jul 2004;10(7):1329-30; author reply 1332-3. [Medline].

  3. MacDonald RD, Krym VF. West Nile virus. Primer for family physicians. Can Fam Physician. Jun 2005;51:833-7. [Medline]. [Full Text].

  4. Petersen LR, Marfin AA. West Nile virus: a primer for the clinician. Ann Intern Med. Aug 6 2002;137(3):173-9. [Medline].

  5. Murray K, Baraniuk S, Resnick M, Arafat R, Kilborn C, Cain K, et al. Risk factors for encephalitis and death from West Nile virus infection. Epidemiol Infect. Dec 2006;134(6):1325-32. [Medline]. [Full Text].

  6. Wadei H, Alangaden GJ, Sillix DH, et al. West Nile virus encephalitis: an emerging disease in renal transplant recipients. Clin Transplant. Dec 2004;18(6):753-8. [Medline].

  7. Zou S, Foster GA, Dodd RY, Petersen LR, Stramer SL. West Nile fever characteristics among viremic persons identified through blood donor screening. J Infect Dis. Nov 1 2010;202(9):1354-61. [Medline].

  8. Abroug F, Ouanes-Besbes L, Letaief M, et al. A cluster study of predictors of severe West Nile virus infection. Mayo Clin Proc. Jan 2006;81(1):12-6. [Medline]. [Full Text].

  9. Nash D, Mostashari F, Fine A, et al. The outbreak of West Nile virus infection in the New York City area in 1999. N Engl J Med. Jun 14 2001;344(24):1807-14. [Medline].

  10. Rodriguez AJ, Westmoreland BF. Electroencephalographic characteristics of patients infected with west nile virus. J Clin Neurophysiol. Oct 2007;24(5):386-9. [Medline].

  11. Rawal A, Gavin PJ, Sturgis CD. Cerebrospinal fluid cytology in seasonal epidemic West Nile virus meningo-encephalitis. Diagn Cytopathol. Feb 2006;34(2):127-9. [Medline].

  12. Tyler KL, Pape J, Goody RJ, et al. CSF findings in 250 patients with serologically confirmed West Nile virus meningitis and encephalitis. Neurology. Feb 14 2006;66(3):361-5. [Medline].

  13. Murray KO, Resnick M, Miller V. Depression after infection with West Nile virus. Emerg Infect Dis. Mar 2007;13(3):479-81. [Medline]. [Full Text].

  14. Ou AC, Ratard RC. One-year sequelae in patients with West Nile Virus encephalitis and meningitis in Louisiana. J La State Med Soc. Jan-Feb 2005;157(1):42-6. [Medline].

  15. Sejvar JJ. The long-term outcomes of human West Nile virus infection. Clin Infect Dis. Jun 15 2007;44(12):1617-24. [Medline].

  16. Cunha BA. Differential diagnosis of West Nile encephalitis. Curr Opin Infect Dis. Oct 2004;17(5):413-20. [Medline].

  17. Cunha BA, Minnaganti V, Johnson DH, Klein NC. Profound and prolonged lymphocytopenia with West Nile encephalitis. Clin Infect Dis. Oct 2000;31(4):1116-7. [Medline].

  18. Cunha BA, Sachdev B, Canario D. Serum ferritin levels in West Nile encephalitis. Clin Microbiol Infect. Feb 2004;10(2):184-6. [Medline].

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Common encephalitis associations.
Clinical features of arboviral encephalitis.
Differential diagnoses of meningoencephalitis.
The Culex mosquito, common in the eastern United States, is the primary vector responsible for infecting humans with West Nile virus. Prevention of West Nile virus is primarily directed at reducing the mosquito population from May to October and by taking precautions to limit human exposure during these months of high mosquito activity. Image courtesy of the Centers for Disease Control and Prevention.
The geographic distribution of the Japanese encephalitis servocomplex of the family Flaviridae, 2000. Image courtesy of the Centers for Disease Control and Prevention.
States reporting laboratory-positive West Nile virus infection in birds, mosquitoes, animals, or humans between January 1 and August 28, 2002. Image courtesy of the Centers for Disease Control and Prevention.
 
 
 
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