Radiosurgery for Epilepsy Associated with Cavernous Malformation: Retrospective Study in 49 Patients

Author:

Régis Jean1,Bartolomei Fabrice1,Kida Yoshihisa2,Kobayashi Tatsuya2,Vladyka Vilibad3,Liscàk Roman3,Forster David4,Kemeny Andras4,Schröttner Oskar5,Pendl Gerhard5

Affiliation:

1. Departments of Stereotactic Neurosurgery and Epileptology, Timone Hospital, Marseilles, France

2. Department of Neurosurgery, Komaki City Hospital, Komaki, Japan

3. Department of Stereotactic Neurosurgery, Hospital Na Homolce, Prague, Czech Republic

4. National Centre for Stereotactic Radiosurgery, Royal Hallamshire Hospital, Sheffield, England

5. Department of Neurosurgery, Karl Franzens University, Graz, Austria

Abstract

Abstract OBJECTIVE Microsurgical resection of a cavernous malformation (CM) with or without associated cortical resection can provide efficient treatment of drug-resistant associated epilepsy. To explore the potential alternative role of radiosurgery and to evaluate its safety and efficacy for this indication, we conducted a retrospective multicenter study. METHODS We retrospectively reviewed the files of patients with long-lasting drug-resistant epilepsy, presumably caused by CM, who were treated by gamma knife (GK) surgery for the control of their epilepsy in five centers (Marseilles, Komaki City, Prague, Graz, and Sheffield). A satisfactory follow-up was available for 49 patients (mean follow-up period, 23.66 ± 13 mo). The mean duration of epilepsy before the GK procedure was 7.5 (±9.3) years. The mean frequency of seizures was 6.9/month (±14). The mean marginal radiation dose was 19.17 Gy ± 4.4 (range, 11.25–36). Among the 49 patients, 17 (35%) had a CM located in or involving a highly functional area. RESULTS At the last follow-up examination, 26 patients (53%) were seizure-free (Engel's Class I), including 24 in Class IA (49%) and 2 patients with occasional auras (Class IB, 4%). A highly significant decrease in the number of seizures was achieved in 10 patients (Class IIB, 20%). The remaining 13 patients (26%) showed little or no improvement. The mediotemporal site was associated with a higher risk of failure. One patient bled during the observation period, and another experienced radiation-induced edema with transient aphasia. Postradiosurgery excision was performed in five patients, and a second radiosurgical treatment was carried out in one patient. CONCLUSION This series is the first to specifically evaluate the capability of GK surgery to safely and efficiently treat epilepsy associated with CM. Seizure control can be reached when a good electroclinical correlation exists between CM location and epileptogenic zone. Although we do not recommend GK surgery for prevention of bleeding for a CM that has not bled previously, our findings suggest that GK surgery can be proposed for the treatment of epilepsy when the CM is located in a highly functional area.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Surgery

Reference39 articles.

1. Surgical management of cerebral cavernous angiomas causing epilepsy;Acciarri;J Neurosurg Sci,1995

2. Special indications: Radiosurgery for functional neurosurgery and epilepsy;Alexander,1993

3. Stereotactic radiosurgery for cavernous malformations: Kjellberg's experience with proton beam therapy in 98 cases at the Harvard Cyclotron;Amin-Hanjani;Neurosurgery,1998

4. Focus irradiation in epilepsy: Experimental study in the cat;Barcia-Salorio;Appl Neurophysiol,1985

5. Supratentorial cavernous angiomas and epileptic seizures: Preoperative course and postoperative outcome;Casazza;Neurosurgery,1996

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