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Published on: April 28, 2019
Acute transverse myelitis (ascending myelitis) as the initial manifestation of Japanese encephalitis: a rare
Varshney Ankur Nandan1, Kumar Nilesh, Behera Dibyaranjan
1IMS BHU, Varanasi, India.
Abstract:
Japanese encephalitis, an inflammatory brain disease prevalent in Southeast Asia, usually presented with fever, headache, convulsions, brain stem signs with pyramidal and extrapyramidal features, and altered sensorium. Acute transverse myelitis, as the initial manifestation of Japanese encephalitis, is an unusual manifestation and is seldom reported. We hereby report a case of 13-year-old adolescent boy who presented to us with fever and acute onset paraparesis with urinary retention initially, progressing to quadriparesis and then followed by headache and altered sensorium. Brain MRI revealed bilateral basal ganglia that were grossly swollen with vasogenic edema tracking along internal capsule and midbrain. Adjacent ventrolateral thalamus and internal capsule also showed mild abnormal intensities. Spinal screening showed abnormal cord intensities in entire cord with gross edema in cervical and conus regions. He had elevated IgM titres against JE virus in cerebrospinal fluid. The patient was treated conservatively along with intravenous methyl prednisolone for 5 days. He regained near normal power at 3 months in followup, but hesitancy, dysarthria, and slowness of movement still persisted. To conclude, a young boy presenting with ATM in an endemic region of JE, then a possibility of Japanese encephalitis, should be sought by clinicians as early use of immunomodulator shows survival benefit.
Insights
Japanese encephalitis (JE) can rarely present as acute transverse myelitis (ATM). Early diagnosis and immunomodulator treatment in JE-endemic regions can improve outcomes for this rare presentation.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Japanese encephalitis (JE) is a common inflammatory brain disease in Southeast Asia.
- Acute transverse myelitis (ATM) is an unusual initial manifestation of JE, rarely reported.
- JE typically presents with fever, headache, seizures, and neurological deficits.
Purpose of the Study:
- To report a rare case of Japanese encephalitis presenting initially as acute transverse myelitis in a 13-year-old boy.
- To highlight the importance of considering JE in patients with ATM in endemic areas.
- To emphasize the potential benefit of early immunomodulator treatment.
Main Methods:
- Case report of a 13-year-old male with fever and acute onset paraparesis.
- Diagnostic workup included brain and spinal MRI, and cerebrospinal fluid (CSF) analysis for JE virus IgM.
- Treatment involved conservative management and intravenous methylprednisolone.
Main Results:
- The patient presented with paraparesis, progressing to quadriparesis, followed by headache and altered sensorium.
- MRI revealed significant edema in the basal ganglia, thalamus, internal capsule, midbrain, and spinal cord.
- CSF analysis confirmed elevated IgM titres against JE virus.
- The patient showed significant motor power recovery at 3 months but persistent neurological deficits.
Conclusions:
- Acute transverse myelitis can be an initial, albeit rare, presentation of Japanese encephalitis.
- Clinicians in JE-endemic regions should consider JE in patients presenting with ATM.
- Early diagnosis and treatment with immunomodulators may improve survival and neurological outcomes.
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