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Association of a sylvian arachnoid cyst and trigonocephaly in a developing child: importance and management
Alp Ozgün Börcek1, Hakan Emmez, Fikret Doğulu
1Department of Neurosurgery, Gazi University, Ankara, Turkey. alpob@yahoo.com
Insights
Trigonocephaly and sylvian arachnoid cysts are rare co-occurrences that can increase intracranial pressure. This case demonstrates successful simultaneous surgical correction of both conditions in an infant.
Area of Science:
- Neurosurgery
- Pediatric Neurosurgery
- Craniofacial Surgery
Background:
- Trigonocephaly (metopic synostosis) and arachnoid cysts can independently cause increased intracranial pressure.
- The combined incidence of trigonocephaly and sylvian arachnoid cysts is not well-documented.
- This report addresses a rare case of this dual pathology.
Observation:
- An 11-month-old girl presented with trigonocephaly (triangular forehead) and a Type II sylvian arachnoid cyst.
- Neurological examination was normal, with no history of seizures or other systemic malformations.
- The patient had metopic suture synostosis.
Findings:
- Surgical intervention involved simultaneous forehead reconstruction (advancement) for trigonocephaly and fenestration of the sylvian arachnoid cyst.
- The arachnoid cyst was fenestrated into the basal cisterns.
- A satisfactory surgical outcome was achieved.
Implications:
- The coexistence of craniosynostosis and arachnoid cysts is uncommon.
- Simultaneous surgical management of trigonocephaly and associated sylvian arachnoid cysts is feasible and effective.
- This approach offers a single-session treatment option for complex pediatric neurosurgical cases.
Introduction:
Trigonocephaly and arachnoid cysts are two different entities that may cause intracerebral pressure elevation: one by space occupying and the other by space restriction. The true incidence of association of trigonocephaly and sylvian arachnoid cyst is not known. We present a rare case of trigonocephaly associated with a sylvian arachnoid cyst in a patient that underwent forehead reconstruction and fenestration of the arachnoid cyst in the same operation.
Case Report:
Investigation of an 11-month-old girl suffering from triangular appearance of the forehead since birth revealed metopic suture synostosis and type II sylvian arachnoid cyst. Neurological examination was normal. There were no seizure history and no other systemic malformation that could be a part of any syndromes associated with cranial synostosis. Forehead reconstruction with forehead advancement for trigonocephaly and fenestration of the arachnoid cyst to the basal cisterns were performed in the same operation. Satisfactory outcome was achieved.
Conclusion:
The coexistence of craniosynostosis and arachnoid cyst is rare. They can be treated surgically in a single session.
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