Effect of vagal nerve stimulation in Dyke-Davidoff-Masson syndrome with refractory generalized seizures - case report
We report a case of Dyke-Davidoff-Masson syndrome (DDMS) in whom left vagal nerve stimulation (VNS) resulted in worthwhile seizure reduction (Engel's Classification Class III). A 20-year-old woman with DDMS whose seizures were medically intractable was successfully treated using left VNS. She w...
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Published in | Turkish neurosurgery Vol. 19; no. 2; pp. 197 - 199 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Turkey
Turkısh Neurosurgery Socıety
01.04.2009
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Abstract | We report a case of Dyke-Davidoff-Masson syndrome (DDMS) in whom left vagal nerve stimulation (VNS) resulted in worthwhile seizure reduction (Engel's Classification Class III). A 20-year-old woman with DDMS whose seizures were medically intractable was successfully treated using left VNS. She was born at term by unsuccessful forceps-assisted vaginal delivery. Her seizures started at the age of 4. There was no detectable mental retardation. Her seizures were intractable although she had been receiving three medications for sixteen years. She underwent left vagal nerve stimulator placement. Pre-stimulation seizure frequency was three seizures per month. This case shows that VNS is an alternative treatment procedure for medically intractable seizures in DDMS. To our knowledge, this is the first case in the world literature reporting worthwhile seizure reduction in DDMS after VNS. |
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AbstractList | We report a case of Dyke-Davidoff-Masson syndrome (DDMS) in whom left vagal nerve stimulation (VNS) resulted in worthwhile seizure reduction (Engel's Classification Class III). A 20-year-old woman with DDMS whose seizures were medically intractable was successfully treated using left VNS. She was born at term by unsuccessful forceps-assisted vaginal delivery. Her seizures started at the age of 4. There was no detectable mental retardation. Her seizures were intractable although she had been receiving three medications for sixteen years. She underwent left vagal nerve stimulator placement. Pre-stimulation seizure frequency was three seizures per month. This case shows that VNS is an alternative treatment procedure for medically intractable seizures in DDMS. To our knowledge, this is the first case in the world literature reporting worthwhile seizure reduction in DDMS after VNS. Bu yazımızda Dyke-Davidoff-Masson sendromu (DDMS) olup sol vagal sinir stimulatörü ile belirgin şekilde nöbetleri azalan (Engel grade III) 20 yaşında kadın hastayı sunduk. Özgeçmişinden forseps yardımı ile zor doğum öyküsü alındı. DDMS tanısı olan hastanın 4 yaşında başlayan ilaca dirençli epilepsi öyküsü mevcuttu. Mental retardasyon tespit edilmedi. Altı yıldır 3'lü antiepileptik ilaç tedavisi almasına rağmen nöbetleri devam etmekteydi. Hastaya soldan vagal sinir stimülatörü takıldı. Postoperatif dönemde hastanın nöbet frekansı ve şiddetinde anlamlı düzelme kaydedildi. Bu vaka ile, DDMS'na bağlı ilaca dirençli epilepsilerde vagal sinir stimülasyonunun, geniş lezyonektomilere önemli bir alternatif olabileceği vurgulanmak istenmiştir. İncelenebildiği kadarı ile bu vaka, medikal literatürde vagal sinir stimülatörü kullanılarak nöbetleri anlamlı ölçüde kontrol edilebilen ilk DDMS vakasıdır. We report a case of Dyke-Davidoff-Masson syndrome (DDMS) in whom left vagal nerve stimulation (VNS) resulted in worthwhile seizure reduction (Engel's Classification Class III). A 20-year-old woman with DDMS whose seizures were medically intractable was successfully treated using left VNS. She was born at term by unsuccessful forceps-assisted vaginal delivery. Her seizures started at the age of 4. There was no detectable mental retardation. Her seizures were intractable although she had been receiving three medications for sixteen years. She underwent left vagal nerve stimulator placement. Pre-stimulation seizure frequency was three seizures per month. This case shows that VNS is an alternative treatment procedure for medically intractable seizures in DDMS. To our knowledge, this is the first case in the world literature reporting worthwhile seizure reduction in DDMS after VNS. |
Author | Acik, Vedat Sarilar, Caner Leventoğlu, Alev Erdem, Atilla Cansu, Ali |
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References | 4. Casazza M, Avanzini G, Ferroli P, Villani F, Broggi G: Vagal nerve stimulation: Relationship between outcome and electroclinical seizure pattern. Seizure 15:198-207, 2006 12. Zilkha A: CT of cerebral hemiatrophy. AJR Am J Roentgenol 135:259-262, 1980 10. Patwardhan RV, Dellabadia J Jr, Rashidi M, Grier L, Nanda A: Control of refractory status epilepticus precipitated by anticonvulsant withdrawal using left vagal nerve stimulation: a case report. Surg Neurol 64:170-173, 2005 2. Ben-Menachem E, Manon-Espaillat R, Ristanovic R, Wilder BJ, Stefan H, Mirza W, et al: Vagus nerve stimulation for treatment of partial seizures: 1.A controlled study of effect on seizures. First International Vagus Nerve Stimulation Study Group. Epilepsia 35:616-626, 1994 9. Parker CE, Harris N, Mavalwala J: Dyke-Davidoff-Masson syndrome: Five case studies and deductions from dermatoglyphics. Clin Pediatr 11:288-292, 1972 11. Sener RN, Jinkins JR: MR of craniocerebral hemiatrophy. Clin Imaging 16:93-97, 1992 7. Labar D, Nikolov B, Tarver B, Fraser R: Vagus nerve stimulation for symptomatic generalized epilepsy: A pilot study. Epilepsia 39:201-205, 1998. 6. George R, Salinsky M, Kuzniecky R, Rosenfeld W, Bergen D, Tarver WB et al: Vagus nerve stimulation for treatment of partial seizures: 3. Long-term follow-up on first 67 patients exiting a controlled study: First International Vagus Nerve Stimulation Study Group. Epilepsia 35:637-643, 1994 5. Dyke CG, Davidoff LM, Masson CB: Cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses. Surg Gynecol Obstet 57:588-600, 1933 8. Nei M, O'Connor M, Liporace J, Sperling MR: Refractory generalized seizures: response to corpus callosotomy and vagal nerve stimulation. Epilepsia 47:115-122, 2006 1. Aguiar PH, Liu CW, Leitao H, Issa F, Lepski G, Figueiredo EG, et al: MR and CT imaging in the Dyke-Davidoff-Masson syndrome. Report of three cases and contribution to pathogenesis and differential diagnosis. Arq Neuropsiquiatr 56:803-807, 1998 3. Buoni S, Mariottini A, Pieri S, Zalaffi A, Farnetani MA, Strambi M, et al: Vagus nerve stimulation for drug-resistant epilepsy in children and young adults. Brain Dev 26:158-163, 2004 |
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Snippet | We report a case of Dyke-Davidoff-Masson syndrome (DDMS) in whom left vagal nerve stimulation (VNS) resulted in worthwhile seizure reduction (Engel's... Bu yazımızda Dyke-Davidoff-Masson sendromu (DDMS) olup sol vagal sinir stimulatörü ile belirgin şekilde nöbetleri azalan (Engel grade III) 20 yaşında kadın... |
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SubjectTerms | Brain - abnormalities Epilepsy, Generalized - etiology Epilepsy, Generalized - pathology Epilepsy, Generalized - therapy Female Hemiplegia - pathology Humans Magnetic Resonance Imaging Vagus Nerve Stimulation Young Adult |
Title | Effect of vagal nerve stimulation in Dyke-Davidoff-Masson syndrome with refractory generalized seizures - case report |
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