Hypothalamic hamartoma with refractory seizures treated with gamma knife surgery: report from tangerang, indonesia
Main Authors: | Simca, Jennifer, Felinsianita, Maria, Nadia, Starry, Ketaren, Retno Jayantri, Hendriansyah, Lutfi, Situmeang, Rocksy FV, Siahaan, Yusak Mangara Tua |
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Format: | Proceeding PeerReviewed Book |
Bahasa: | eng |
Terbitan: |
, 2018
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Subjects: | |
Online Access: |
http://repository.uph.edu/3010/1/3.5._AOEC_2018.pdf http://repository.uph.edu/3010/2/B3.5_Peer_Review%20Result.pdf http://repository.uph.edu/3010/3/3.5_Publication%20Agreement.pdf http://repository.uph.edu/3010/ |
Daftar Isi:
- Hypothalamic hamartoma (HH) is a rare, slowly growing benign lesion arising from the floor of the third ventricle, tuber cinereum, or mammillary bodies. The incident of HH is 1 in 50,000 - 100,000 births which is often associated with gelastic seizures, cognitive impairment, behavioral distubances, and central precocious puberty. (Esquenazi et al. J Neurosurg Pediatrics 2013;11:630-634.) Gelastic sizures associated with HH are generally intractable to standard antiepileptic drugs. Gamma knife surgery has emerged as an alternative to microsurgical removal or radiofrequency ablation to improve seizure control.