Noradrenaline in Artery Walls and its Dispersal by Reserpine
Норадреналин в стенках артерий и его рассеивание под действием резерпина
1958-04-19
SCID: 54.1/yyse7sw9
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Anton-Babinski syndromeWest Nile encephalitisneuroinvasive West Nile diseaseposterior reversible encephalopathy syndromevisual anosognosia
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Abstract (AI)
Objective: N/A. Background: West Nile virus (WNV) first emerged in the late 1990s in the United States. Since then upwards of 23,000 cases have been reported. Presentation of WNV varies from West Nile fever in approximately 20% of patients to West Nile neuroinvasive disease in less than 1% of infected individuals. Here we present a patient with neuroinvasive West Nile encephalitis who presented with Anton-Babinski syndrome (ABS). Design/Methods: A 55-year-old female with a past medical history of hypertension, hypothyroidism, hyperlipidemia and CKD presented to a community hospital in the Summer with sudden acute onset of fevers, chills, and altered mental status. Vital signs were significant for a fever of 39.0 C, and blood pressure 180/112. Laboratory results were significant for elevated white blood cell count of 22,000/ul. Neurologic exam was significant for altered mental status (oriented only to self). MRI brain revealed T2/FLAIR hyperintensities in the fontal, temporal, and occipital cortices. A lumbar puncture was completed with concern for autoimmune encephalitis which had returned negative. A preliminary diagnosis of posterior-reversible encephalopathy syndrome (PRES) was made. After 8 weeks with no significant improvement the patient was transferred to a tertiary care center. Physical exam was notable for no response to visual threat, equal and reactive pupils, and visual anosognosia with confabulations. A repeat MRI showed interval progression of the previously defined lesions. A repeat LP with clear CSF was obtained and serum blood test revealed an elevated WNV IgG, CSF and serum of 1.89 and 2.62 respectively. Based on clinical progression and prognosis of WNV the patient was referred to a long term care facility. Results: N/A. Conclusions: Neuroinvasive West Nile disease remains to be a rare diagnosis and it’s radiographic and clinical presentation vary. This case aims to highlight the importance of early diagnosis and recognition of symptoms to improve clinical outcomes. Disclosure: Dr. Srichawla has nothing to disclose. Dr. Min has nothing to disclose.
Key Findings
1
A 55-year-old woman developed neuroinvasive West Nile encephalitis presenting with Anton-Babinski syndrome, including visual anosognosia and confabulation.
2
Brain MRI showed progressive T2/FLAIR hyperintensities involving the frontal, temporal, and occipital cortices.
3
Elevated West Nile virus IgG in both cerebrospinal fluid and serum supported the diagnosis of neuroinvasive West Nile disease.
4
Initial evaluation suggested posterior reversible encephalopathy syndrome, but lack of improvement over eight weeks and progressive MRI abnormalities prompted reconsideration.
5
The case underscores the variable clinical and radiographic presentation of neuroinvasive West Nile disease and the importance of early recognition.
Research Object
A patient with neuroinvasive West Nile virus encephalitis presenting with Anton-Babinski syndrome
Research Subject
The clinical and radiographic presentation and diagnostic recognition of Anton-Babinski syndrome in neuroinvasive West Nile disease
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1958-04-19
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