Published online Nov 16, 2014. doi: 10.12998/wjcc.v2.i11.623
Revised: September 17, 2014
Accepted: October 1, 2014
Published online: November 16, 2014
Processing time: 104 Days and 11.4 Hours
Long-term epilepsy associated tumors (LEAT) represent a well known cause of focal epilepsies. Glioneuronal tumors are the most frequent histological type consisting of a mixture of glial and neuronal elements and most commonly arising in the temporal lobe. Cortical dysplasia or other neuronal migration abnormalities often coexist. Epilepsy associated with LEAT is generally poorly controlled by antiepileptic drugs while, on the other hand, it is high responsive to surgical treatment. However the best management strategy of tumor-related focal epilepsies remains controversial representing a contemporary issues in epilepsy surgery. Temporo-mesial LEAT have a widespread epileptic network with complex epileptogenic mechanisms. By using an epilepsy surgery oriented strategy LEAT may have an excellent seizure outcome therefore surgical treatment should be offered early, irrespective of pharmacoresistance, avoiding both the consequences of uncontrolled seizures as well as the side effects of prolonged pharmacological therapy and the rare risk of malignant transformation.
Core tip: Long-term epilepsy associated tumors (LEAT) represent a frequent cause of focal epilepsies, particularly in children and young adults. Epilepsy associated with LEAT is generally poorly controlled by antiepileptic drugs while it is extremely responsive to surgical treatment. Temporo-mesial LEAT have a widespread epileptic network and complex epileptogenic mechanisms. The best management strategy of tumor-related focal epilepsies remains controversial representing a contemporary issues in epilepsy surgery.