Research Article
Paediatric Intracranial Arachnoid Cysts: Single Institutional Review and Outcome
Abstract
Background: Intracranial arachnoid cysts in the paediatric neurosurgical patient are a common diagnostic quagmire. Though commonly an incidental finding, they are a continuous source of anxiety for both patient’s families and the managing clinician. The symptoms often attributed to their presence are also often varied and do range from nonspecific headache or behavioural changes to life threatening hydrocephalus or intracystic haemorrhage. Materials and Methods: We present a 6-year retrospective review and analysis of cases of intracranial arachnoid cysts diagnosed at a single centre tertiary care paediatric neurosciences unit. An analysis of medical records and review of images was performed. Results: A total of 167 cases were identified over a period of 6 years, with 69% being males and 31% females. Age at diagnosis varied from 1 day of life to 17 yrs. Follow up duration has been up to 11 years. Presentation varied from incidental finding, headaches (7.8%), seizures (2.4%), vomiting (2.4%), behavioural anomalies to decreased level of consciousness (1.2%). On radiological imaging, majority were located in the skull base: middle cranial fossa (55.1%) and posterior cranial fossa (38.9%). Medical and expectant management of these patients was the primary mode of care, with surgical intervention only needed in cases characterized by either hydrocephalus, significant mass effect with features of raised ICP or in cases of intracystic haemorrhage. Conclusion: Arachnoid cysts genera