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Published on: March 7, 2017
Pediatric gliomatosis cerebri mimicking tubercular encephalitis
Namit Singhal1, Vinay Agarwal2
1Department of Neurosciences, SS Hospital, Agra, Uttar Pradesh, India.
Insights
Gliomatosis cerebri (GC) in children is rare and challenging to diagnose, often mimicking other conditions. Histological evaluation is crucial for accurate diagnosis, especially when neuroimaging is inconclusive.
Area of Science:
- Neuro-oncology
- Pediatric Neurology
Background:
- Gliomatosis cerebri (GC) is a rare, diffuse glial neoplasm of astrocytic origin.
- Pediatric GC presents diagnostic challenges due to varied symptoms mimicking other conditions.
Observation:
- A pediatric case initially treated for tubercular encephalitis showed transient improvement.
- Neuroimaging revealed temporary resolution of the enhancing component, complicating diagnosis.
Findings:
- Clinical presentation and neuroimaging have limitations in diagnosing pediatric GC.
- Histological evaluation is essential for definitive diagnosis of GC in children.
- A subset of patients with Ki index <10% may experience a protracted course after radiotherapy.
Implications:
- Emphasizes the critical need for early and accurate diagnosis of pediatric GC.
- Suggests a potential for a more benign clinical course in specific pediatric GC cases.
- Highlights the necessity for collaborative efforts in managing and researching rare pediatric GC cases.
Abstract:
Gliomatosis cerebri (GC) is a diffuse infiltrating glial neoplasm of astrocytic origin. GC in children is rare and difficult to diagnose, often presenting with a variety of signs and symptoms that may mimic myriad conditions. We discuss here the presentation and diagnosis of GC in a child who was initially treated on lines of tubercular encephalitis, with transient clinical relief and disappearance of enhancing component of the disease on magnetic resonance imaging. In this report, we highlight the limitations of clinical presentation and neuroimaging as well as the essential role of histological evaluation for the diagnosis of GC in children. Also is highlighted a more benign and protracted clinical course following radiotherapy in a subset of patients, with Ki index <10%, thereby stressing earliest possible diagnosis. A new prognostic classification can also be proposed for pediatric GC based on various parameters. Since these are rare cases, a combined effort is required for this.
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