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Published on: October 20, 2017
A Case of Bilateral Cerebellar Chronic Encapsulated Intracerebral Hematoma with Rapidly Progressive Symptoms
Azuna Tomioka1, Satoshi Takahashi1, Ryotaro Imai1
1Department of Neurosurgery, Keio University School of Medicine, Tokyo, Japan.
Insights
This case report details a rare instance of bilateral cerebellar chronic encapsulated intracerebral hematoma (CEIH). Prompt surgical intervention led to a satisfactory outcome, highlighting the importance of recognizing this condition.
Area of Science:
- Neurology
- Neurosurgery
- Vascular Neurology
Background:
- Chronic encapsulated intracerebral hematoma (CEIH) is a rare cerebrovascular condition characterized by progressive hematoma expansion.
- Diagnosis can be challenging due to its rarity and subtle presentation.
Observation:
- A man in his 70s presented with dizziness and bilateral cerebellar space-occupying lesions.
- Rapid symptom progression and signs of cerebellar herniation necessitated emergency surgery.
Findings:
- Preoperative imaging (MRI, CT) and pathological findings confirmed bilateral cerebellar CEIH with partial capsulation.
- This represents the first reported case of bilateral cerebellar CEIH in the literature.
Implications:
- Early recognition and surgical treatment of CEIH are crucial for favorable patient outcomes.
- Neurosurgeons should consider CEIH in the differential diagnosis of cerebellar hemorrhages, especially when progressive expansion is suspected.
Abstract:
Chronic encapsulated intracerebral hematoma (CEIH) is a rare cerebrovascular disease featuring progressively expanding intracranial hematoma. We treated a man in his 70s with bilateral cerebellar CEIH. He had presented at another hospital with dizziness, and imaging showed two independent hemorrhagic space-occupying lesions in the bilateral cerebellar hemispheres. The symptoms progressed relatively rapidly, and there were signs of impending cerebellar herniation; he was transferred to our institution, and emergency surgery was performed. The operative findings included a hematoma with partial capsulation. We diagnosed CEIH from preoperative magnetic resonance imaging and computed tomography findings, clinical course, and pathological findings. The postoperative course was satisfactory. We present this case of bilateral cerebellar CEIH, as an extensive search of the literature suggests that this has not been reported before. Although CEIH is a condition that is usually hard to diagnose preoperatively, good outcomes can be achieved with appropriate surgical treatment. It is therefore important to keep this clinical entity in mind and not miss the right timing to operate.
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