Diagnosis and Management of Epilepsy Associated With Hypothalamic Hamartoma: An Evidence-Based Systematic Review
Department
neurology
Document Type
Article
Abstract
The main objective was to review the evidence for management of epilepsy associated with hypothalamic hamartomas. We performed a systemic review of the literature through July 2012 that studied patients with hypothalamic hamartomas and related epilepsy. Articles meeting selection criteria were rated according to the American Academy of Neurology classification of evidence scheme. Recommendations were linked to the strength of the evidence and as follows: (a) precocious puberty is associated more with the pedunculated type and epilepsy typified by gelastic seizures with the sessile form of hypothalamic hamartomas (class III); (b) significant behavioral and cognitive deficits are associated with patients with hypothalamic hamartomas (class III); (c) video electroencephalography (EEG) findings are extremely variable particularly across the different ages and do not affect surgical outcome (class III); d) various surgical techniques (transcallosal and endoscopic resection) resulted in 49% to 54% seizure freedom, 15% with a pterional approach as well as about 40% with radiosurgery (class III).
Medical Subject Headings
neurology
Publication Date
2013
Publication Title
Journal of Child Neurology
ISSN
0883-0738
Volume
28
Issue
7
First Page
909
Last Page
916
PubMed ID
23670254
Digital Object Identifier (DOI)
10.1177/0883073813488673
Recommended Citation
Pati, Sandipan; Sollman, Myriam; Fife, Terry D.; and Ng, Yu Tze, "Diagnosis and Management of Epilepsy Associated With Hypothalamic Hamartoma: An Evidence-Based Systematic Review" (2013). Neurology. 77.
https://scholar.barrowneuro.org/neurology/77