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HERO ID
6408704
Reference Type
Journal Article
Title
Giant hypothalamic hamartoma operated through subfrontal approach with orbitary rim osteotomy
Author(s)
Miranda, P; Esparza, J; Cabrera, A; Hinojosa, J
Year
2006
Is Peer Reviewed?
1
Journal
Pediatric Neurosurgery
ISSN:
1016-2291
EISSN:
1423-0305
Volume
42
Issue
4
Page Numbers
254-257
Language
English
PMID
16714869
DOI
10.1159/000092365
Web of Science Id
WOS:000243060700011
Abstract
INTRODUCTION:
Hypothalamic hamartomas are associated with precocious puberty, gelastic seizures and severe refractory epilepsy. Treatment options include surgical resection, radiofrequency and radiosurgery.
CASE REPORT:
A 7-month-old girl presented with gelastic seizures and developmental delay related to a giant hypothalamic hamartoma. The patient was operated through a subfrontal approach. Intraoperatively the lesion appeared intimately adherent to the right internal carotid artery. Seizure control was improved after tumoral decompression.
CONCLUSIONS:
Treatment of giant hypothalamic hamartomas should always include surgical resection, given the mass effect over surrounding vital structures. Subfrontal approach with orbitary rim osteotomy provides a wide exposure with minimal frontal lobe retraction. Close adherence of hypothalamic hamartoma to vascular structures may be present, requiring careful surgical manipulation.
Keywords
giant hypothalamic hamartoma, subfrontal approach; gelastic seizures
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