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|Title:||Long-term seizure outcome following surgery for dysembryoplastic neuroepithelial tumor.||Austin Authors:||Chan, Chow Huat;Bittar, Richard G;Davis, Gavin A ;Kalnins, Renate M;Fabinyi, Gavin C||Affiliation:||Neurosurgical Department, Austin Hospital, Heidelberg, Victoria, Australia||Issue Date:||1-Jan-2006||Publication information:||Journal of Neurosurgery; 104(1): 62-9||Abstract:||Resection of dysembryoplastic neuroepithelial tumor (DNET) is thought to result in favorable seizure outcome, but long-term follow-up data are scarce. The authors present a review of 18 patients who underwent surgical removal of a DNET: 12 via temporal lobectomy and six via lesionectomy.The mean long-term follow up was 10.8 years (median 10.4 years, range 7.8 to 14.8 years), and results obtained during this time period were compared with previously reported short-term (mean 2.7 years) seizure outcome data. In the current study, 66.7% patients had an Engel Class I outcome and 55.6% had an Engel Class IA outcome compared with 77.8% and 55.6%, respectively. Temporal lobectomy (Engel Class I, 83.3%; Engel Class IA, 66.7%) led to a better seizure outcome than lesionectomy (Engel Classes I and IA, 33.3%). Two patients (11.1%) required repeated operation and both had an incomplete lesionectomy initially.Results indicated that complete resection of a DNET leads to a favorable seizure outcome, with epilepsy cure in those who had experienced early postoperative seizure relief. Long-term seizure outcome after surgery is predictable based on the result of short-term follow up.||URI:||http://ahro.austin.org.au/austinjspui/handle/1/10108||DOI:||10.3171/jns.2006.104.1.62||URL:||https://pubmed.ncbi.nlm.nih.gov/16509148||Type:||Journal Article||Subjects:||Adolescent
Severity of Illness Index
|Appears in Collections:||Journal articles|
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