WNE, West Nile Encephalitis

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kkkClinic

  • It is a viral miasm
  • In 80%, it show no symptoms and mostly recover completely, though Fatigue / Weakness may last for Weeks / Months.
  • Symptoms may range from fever to paralysis and meningitis.
  • Sever infection can rarely cause permanent brain damage.
  • The most common neuromuscular manifestation is a poliomyelitis syndrome with or without brain-stem involvement (Respiratory failure)
  • Significant neurological deficits are [1]
    • 49% Weakness
    • 35% Tremor
    • 16% Cranial neuropathy


Entities
Poliomyelitis [2] GBS [2]
Encephalitis
Myositis
Polyradiculitis Brachial plexopathy [5]
  • Spinal sympathetic ganglianopathy (Autonomic instability) [6]
Rapid pulse, Flushed Face, Coldness of feet)


  • Splenomegaly: Leukopenia
  • Hepatitis: Hepatomegaly, Nausea, Vomiting, Loss of appetite, and Diarrhea
  • Pancreatitis: Diarrhea
  • Eruptions: maculopapular, pale roseolar
  • Hyponatremia
  • Lying in bed agg. Night agg
  • Eye Pain. Injected


WNND

  • West Nile Neuroinvasive Disease occurs in less than 1% of cases, resulting in meningitis, encephalitis, meningoencephalitis or a poliomyelitis-like syndrome.
  • Often there is normal neuroimaging, although abnormalities including basal ganglia, thalamus, cerebellum, and brain-stem have been reported
  • Muscular weakness + Lower motor neuron symptoms, Flaccid paralysis, + Hyporeflexia +No sensory abnormalities.[7]


WNP

  • West Nile Poliomyelitis is an acute flaccid paralysis syndrome associated with WNV
  • It is less common than WNM or WNE.
  • It is generally characterized by the acute onset of Asymmetric limb weakness or paralysis in the absence of sensory loss.
  • Pain sometimes precedes the paralysis. The paralysis can occur in the absence of fever, headache, or other common symptoms associated with WNV infection.
  • Involvement of respiratory muscles, leading to acute respiratory failure, sometimes occurs.
  • West-Nile reversible paralysis, Like WNP, the weakness or paralysis is asymmetric. Reported cases have been noted to have an initial preservation of deep tendon reflexes, which is not expected for a pure anterior horn involvement.
  • Disconnect of upper motor neuron influences on the anterior horn cells possibly by myelitis or glutamate excitotoxicity have been suggested as mechanisms.[7]
  • Typical WNE paralysis is characterized by muscle weakness, decreased tone, and loss of deep tendon reflexes attributed to destruction of anterior horn cells.[8]


Disease


Remedies

  1. IOD, MERC. PHOS
  2. Bell, Caust.  Cupr. Plb. Sil. Sulph.
  3. agar, aur. Calc con gels kali-c


  1. Hart, J., Tillman, G., Kraut, M.A. et al. West Nile virus neuroinvasive disease: neurological manifestations and prospective longitudinal outcomes. BMC Infect Dis 14, 248 (2014). https://doi.org/10.1186/1471-2334-14-248
  2. 2.0 2.1 A Wolf in Sheep’s Clothing: West Nile Virus presenting as Guillain Barre Variant (P11-9.005) Subhan Tabba, Asif Kabani Neurology May 2022, 98 (18 Supplement) 3438;
  3. https://www.encephalitis.info/
  4. Paul J. Carson, Patrick Konewko, Kimberly S. Wold, Paul Mariani, Sunil Goli, Paula Bergloff, Ross D. Crosby, Long-Term Clinical and Neuropsychological Outcomes of West Nile Virus Infection, Clinical Infectious Diseases, Volume 43, Issue 6, 15 September 2006, Pages 723–730,
  5. Madden K. West Nile virus infection and its neurological manifestations. Clin Med Res. 2003 Apr;1(2):145-50. doi: 10.3121/cmr.1.2.145. PMID: 15931302; PMCID: PMC1069038.
  6. Budhram A, Sharma M, Shettar B, Hosseini-Moghaddam SM, Khaw AV. Sensory and autonomic involvement in West Nile virus-associated acute flaccid paralysis. Neurol Clin Pract. 2017 Oct;7(5):394-397. doi: 10.1212/CPJ.0000000000000373. PMID: 29620087; PMCID: PMC5874468.
  7. 7.0 7.1 Wikipedia
  8. Mojumder DK, Agosto M, Wilms H, Kim J. Is initial preservation of deep tendon reflexes in West Nile Virus paralysis a good prognostic sign? Neurol Asia. 2014 Mar;19(1):93-97. PMID: 25400704; PMCID: PMC4229851.
  9. REVIEW article Front. Neurol., 21 March 2012 Sec. Neuromuscular Disorders and Peripheral Neuropathies https://doi.org/10.3389/fneur.2012.00037