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Updated: May 23, 2026

Minimally Invasive Endoscopic Intracerebral Hemorrhage Evacuation
Published on: October 15, 2021
Intracranial hypertension with polyradiculopathy--early CSF diversion to optimize neurological recovery
Sapna Erat Sreedharan1, Pournamy Sarathchandran, Girish Menon
1Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Medical College PO, Trivandrum, Kerala, India. sapnaerat@yahoo.com
Insights
Cerebral venous sinus thrombosis and idiopathic intracranial hypertension can cause high intracranial pressure. Two patients with severe neurological symptoms recovered fully after cerebrospinal fluid diversion.
Area of Science:
- Neurology
- Ophthalmology
Background:
- Cerebral venous sinus thrombosis (CVST) and idiopathic intracranial hypertension (IIH) are differential diagnoses for young patients with isolated intracranial hypertension.
- Raised intracranial pressure (ICP) can lead to significant neurological deficits.
Observation:
- Two patients presented with progressive visual failure and polyradiculopathy with areflexic quadriparesis.
- These symptoms were secondary to significantly raised ICP.
Findings:
- Both patients underwent cerebrospinal fluid diversion.
- Complete neurological recovery was observed in both cases following the intervention.
Implications:
- Fulminant presentations of raised ICP with severe neurological compromise can have excellent outcomes.
- Cerebrospinal fluid diversion is an effective treatment for specific cases of severe raised ICP.
- Highlights the importance of considering and managing raised ICP in young patients with neurological symptoms.
Abstract:
Cerebral venous sinus thrombosis (CVST) and idiopathic intracranial hypertension (IIH) are common considerations in young patients presenting with isolated intracranial hypertension. We report two patients with progressive visual failure and polyradiculopathy with areflexic quadriparesis, secondary to raised intracranial pressure (ICP). Both underwent cerebrospinal fluid diversion with complete recovery. Such a fulminant presentation of raised ICP with an excellent outcome has rarely been reported in the literature.
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