Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy

Abstract Forel‐H‐tomy for intractable epilepsy was introduced by Dennosuke Jinnai in the 1960s. Recently, Forel‐H‐tomy was renamed to “pallidothalamic tractotomy” and revived for the treatment of Parkinson's disease and dystonia. Two of our patients with movement disorders and comorbid epilepsy...

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Main Authors: Shiro Horisawa, Satoru Miyao, Tomokatsu Hori, Kotaro Kohara, Takakazu Kawamata, Takaomi Taira
Format: Article
Language:English
Published: Wiley 2021-03-01
Series:Epilepsia Open
Subjects:
Online Access:https://doi.org/10.1002/epi4.12467
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author Shiro Horisawa
Satoru Miyao
Tomokatsu Hori
Kotaro Kohara
Takakazu Kawamata
Takaomi Taira
author_facet Shiro Horisawa
Satoru Miyao
Tomokatsu Hori
Kotaro Kohara
Takakazu Kawamata
Takaomi Taira
author_sort Shiro Horisawa
collection DOAJ
description Abstract Forel‐H‐tomy for intractable epilepsy was introduced by Dennosuke Jinnai in the 1960s. Recently, Forel‐H‐tomy was renamed to “pallidothalamic tractotomy” and revived for the treatment of Parkinson's disease and dystonia. Two of our patients with movement disorders and comorbid epilepsy experienced significant seizure reduction after pallidothalamic tractotomy, demonstrating the efficacy of this method. The first was a 29‐year‐old woman who had temporal lobe epilepsy with focal impaired awareness seizure once every three months and an aura 10‐20 times daily, even with four antiseizure medicines. For the treatment of hand dyskinesia, she underwent left pallidothalamic tractotomy and her right‐hand dyskinesia significantly improved. Fourteen months later, she had experienced no focal impaired awareness seizure and the aura decreased to one to three times per month. The second case was that of a 15‐year‐old boy diagnosed with progressive myoclonic epilepsy, who developed generalized tonic‐clonic seizure, which manifested once every month, despite treatment with five antiseizure medicines. After surgery, myoclonic movements in his right hand slightly improved. A one‐year follow‐up revealed that he had not experienced a generalized tonic‐clonic seizure. The lesion locations in the two cases were close to the vicinity of Jinnai's Forel‐H‐tomy. Forel's field H deserves reconsideration as a treatment target for intractable epilepsy.
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spelling doaj.art-42074eaf4d5c48828599de5314ea81c02022-12-21T21:26:21ZengWileyEpilepsia Open2470-92392021-03-016122522910.1002/epi4.12467Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomyShiro Horisawa0Satoru Miyao1Tomokatsu Hori2Kotaro Kohara3Takakazu Kawamata4Takaomi Taira5Department of Neurosurgery Tokyo Women’s Medical University Tokyo JapanDepartment of Neurosurgery Tokyo Women’s Medical University Tokyo JapanDepartment of Neurosurgery Moriyama Neurological Center Hospital Tokyo JapanDepartment of Neurosurgery Tokyo Women’s Medical University Tokyo JapanDepartment of Neurosurgery Tokyo Women’s Medical University Tokyo JapanDepartment of Neurosurgery Tokyo Women’s Medical University Tokyo JapanAbstract Forel‐H‐tomy for intractable epilepsy was introduced by Dennosuke Jinnai in the 1960s. Recently, Forel‐H‐tomy was renamed to “pallidothalamic tractotomy” and revived for the treatment of Parkinson's disease and dystonia. Two of our patients with movement disorders and comorbid epilepsy experienced significant seizure reduction after pallidothalamic tractotomy, demonstrating the efficacy of this method. The first was a 29‐year‐old woman who had temporal lobe epilepsy with focal impaired awareness seizure once every three months and an aura 10‐20 times daily, even with four antiseizure medicines. For the treatment of hand dyskinesia, she underwent left pallidothalamic tractotomy and her right‐hand dyskinesia significantly improved. Fourteen months later, she had experienced no focal impaired awareness seizure and the aura decreased to one to three times per month. The second case was that of a 15‐year‐old boy diagnosed with progressive myoclonic epilepsy, who developed generalized tonic‐clonic seizure, which manifested once every month, despite treatment with five antiseizure medicines. After surgery, myoclonic movements in his right hand slightly improved. A one‐year follow‐up revealed that he had not experienced a generalized tonic‐clonic seizure. The lesion locations in the two cases were close to the vicinity of Jinnai's Forel‐H‐tomy. Forel's field H deserves reconsideration as a treatment target for intractable epilepsy.https://doi.org/10.1002/epi4.12467Forel‐H‐tomypallidothalamic tract
spellingShingle Shiro Horisawa
Satoru Miyao
Tomokatsu Hori
Kotaro Kohara
Takakazu Kawamata
Takaomi Taira
Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy
Epilepsia Open
Forel‐H‐tomy
pallidothalamic tract
title Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy
title_full Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy
title_fullStr Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy
title_full_unstemmed Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy
title_short Comorbid seizure reduction after pallidothalamic tractotomy for movement disorders: Revival of Jinnai’s Forel‐H‐tomy
title_sort comorbid seizure reduction after pallidothalamic tractotomy for movement disorders revival of jinnai s forel h tomy
topic Forel‐H‐tomy
pallidothalamic tract
url https://doi.org/10.1002/epi4.12467
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