Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6006527 | Clinical Neurology and Neurosurgery | 2013 | 8 Pages |
ObjectivePituicytoma is a rare, benign, primary tumour, almost all of which occur in adults. Here, we present one case of giant pituicytoma in a boy and a review literature to assist in understanding its natural history, behaviour, clinicopathological features and treatment options.MethodsA PUBMED search using the keywords “pituicytoma” was performed, and the citations were reviewed.ResultsWe found 65 cases of pituicytomas, including our report, in the international literature to date; among these cases, only three were diagnosed in patients under 14 years old.ConclusionPituicytoma is a slow-growing, rare, low-grade glial neoplasm that originates in the neurohypophysis. Currently, the optimal treatment is gross total resection, and confirmed diagnosis relies upon pathological tests. Regular MRI follow-up is recommended.