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A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Associated with Dengue Infection in a Child
Ranjith Kumar Manokaran1, Harshavardhan Mahalingam2, Shubha Shankaranarayanan3
1Division of Pediatric Neurology, Department of Neurology, Sri Ramachandra Institute of Higher Education and Research, Porur, Chennai 600116, India.
Insights
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a rare neurological condition. This case highlights dengue infection as a potential cause of AESD in infants, successfully treated with immunoglobulin therapy.
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a recognized clinico-radiological syndrome in children.
- Commonly associated with viral and bacterial infections, AESD's link to dengue has not been previously documented.
Observation:
- A 9-month-old infant presented with fever, seizures, and gastrointestinal symptoms.
- Recurrent seizures occurred after an afebrile interval, with non-contributory cerebrospinal fluid analysis.
- Laboratory tests confirmed dengue infection.
Findings:
- Brain MRI revealed characteristic diffusion restriction in the bilateral frontal and parietal white matter, with perisylvian sparing, indicative of AESD.
- The infant showed complete recovery following treatment with intravenous human immunoglobulin therapy.
Implications:
- This case report expands the known neurological manifestations of dengue infection.
- It suggests that dengue should be considered in the differential diagnosis of AESD, particularly in endemic regions.
- Intravenous immunoglobulin therapy may be a potential treatment option for AESD secondary to dengue.
Abstract:
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a clinico-radiological syndrome in children secondary to viral or bacterial infections. The causes include viral (influenza, human herpes virus-6, adenovirus, rota) as well as bacterial infections. However, AESD with dengue infection has not been reported earlier. Here, we present an infant with dengue infection and AESD which recovered completely following treatment with intravenous human immunoglobulin therapy. A 9-month-old girl presented with seizures following fever and loose stools. Seizures recurred after 2 days of seizure-free interval. Cerebrospinal fluid analysis was not contributory. Dengue infection was confirmed by lab tests. Magnetic resonance imaging brain after the second seizure revealed diffusion restriction involving the bilateral frontal and parietal white matter, both hemispheres with a typical central perisylvian sparing lesion suggestive of AESD. This case report expands the reported spectrum of neurological manifestations of dengue infection.
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