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Published on: July 24, 2016
Dengue cerebellitis in middle childhood from South India
Venkatesh Kumar Balan1, Sarala Premkumar2, Elayaraja Sivaprakasam2
1Paediatric Medicine, Sri Ramachandra Institute of Higher Education and Research, Chennai, India drvk@sriramachandra.edu.in.
Insights
Dengue fever can rarely cause cerebellitis, a rare neurological complication. Prompt diagnosis and supportive care led to a full recovery in a pediatric patient.
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Dengue fever is a common arboviral illness in tropical regions.
- Neurological manifestations of dengue fever are infrequent but can be severe.
- Cerebellitis, inflammation of the cerebellum, is a rare complication of dengue infection.
Purpose of the Study:
- To report a rare case of dengue-associated cerebellitis in a child.
- To highlight the importance of considering atypical presentations of dengue fever.
- To emphasize the role of timely diagnosis in managing neurological complications of dengue.
Main Methods:
- A case study of a middle childhood girl presenting with symptoms suggestive of dengue fever.
- Clinical examination including funduscopy and neuroimaging (MRI brain) were performed.
- Laboratory investigations including dengue IgM antibody testing, liver function tests, and ferritin levels were conducted.
Main Results:
- The patient presented with prolonged fever, vomiting, abdominal pain, and signs of shock.
- Neurological signs including nystagmus, diplopia, dizziness, and papilledema developed.
- MRI revealed cerebellar hyperintensity consistent with cerebellitis; dengue IgM was positive.
- The patient recovered with supportive care and anti-edema measures.
Conclusions:
- Dengue fever can present with rare neurological complications such as cerebellitis.
- Early recognition and management of cerebellitis in dengue are crucial for favorable outcomes.
- This case underscores the diverse clinical spectrum of dengue virus infection.
Abstract:
We had a girl in middle childhood, who presented with fever of 7 days duration, vomiting, abdominal pain, headache, myalgia and arthralgia. The child was conscious with signs of shock. With the provisional diagnosis of dengue fever, enteric fever or scrub typhus, the child was given all supportive management. Lab investigations covering the fever panel were sent. Within 24 hours of admission, the child developed horizontal nystagmus, diplopia and intermittent dizziness. Fundus examination showed papilloedema. MRI brain showed hyperintensity of the cerebellum in T2 sections suggestive of cerebellitis. Dengue IgM antibody was positive with transaminitis and hyperferritinaemia. Child was given anti-oedema measures with supportive care. The patient recovered on day 10 of illness, and cerebellar signs subsided. Though dengue fever is commonly seen in tropical countries, the atypical presentation in the form of cerebellitis is found to be rare. The timely diagnosis helped in rapid recovery from this neurological manifestation.
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