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Published on: February 29, 2020
[A spontaneous bilateral subdural effusion in an 11-year-old boy with middle cranial fossa arachnoid cyst]
Tomohiro Kumada1, Kozo Mutoh, Masakazu Sakaguchi
1Department of Pediatrics, Shimada Municipal Hospital, Shimada, Shizuoka. tkuma@k6.dion.ne.jp
Insights
A pediatric patient experienced symptoms of increased intracranial pressure due to an arachnoid cyst. Surgical fenestration relieved the pressure and subdural effusion, highlighting a rare complication of arachnoid cysts.
Area of Science:
- Pediatric Neurology
- Neurosurgery
- Neuroimaging
Background:
- Intracranial arachnoid cysts are common congenital malformations.
- While typically benign, they can rarely lead to complications such as subdural effusion and intracranial hypertension.
Observation:
- An 11-year-old boy presented with a month of headache, vomiting, and diplopia.
- Head CT revealed a right middle cranial fossa arachnoid cyst and bilateral subdural effusion.
- Papilledema developed, and lumbar puncture showed markedly elevated cerebrospinal fluid pressure (800 mmH2O).
Findings:
- A small tear in the arachnoid cyst wall was identified, likely creating a communication pathway with the subdural space.
- Fenestration of the cyst to the basal cisterns rapidly resolved the patient's symptoms and subdural effusion.
Implications:
- This case demonstrates a rare, non-traumatic cause of subdural effusion and intracranial hypertension in a child.
- Arachnoid cyst fenestration is an effective treatment for associated intracranial hypertension and effusion.
- The etiology of the cyst wall tear remains unclear, emphasizing the need for vigilance in diagnosing such complications.
Abstract:
An 11-year-old boy gradually developed headache, vomiting and diplopia over a period of 1 month. Repeated examinations of head CT scan revealed an arachnoid cyst in the right middle cranial fossa and bilateral subdural effusion of enlarging size. Papilledema was absent on admission, but it became evident after 1 week, and lumbar puncture disclosed very high pressure (800 mmH2O) of the cerebrospinal fluid. Fenestration of the cyst to the basal cisterms quickly alleviated his symptoms of intracranial hypertension as well as the bilateral subdural effusion on CT. Macroscopically, there was a small tear on the wall of the arachnoid cyst, and it probably served as a communication valve with the subdural space. Since he had no history of head trauma in the past few months, the reason of the tear formation was unclear. Intracranial arachnoid cyst is a relatively common congenital malformation of usually benign and non-pathogenic nature. However, it may occasionally cause non-traumatic subdural effusion and intracranial hypertension.
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