A case of hemiplegic migraine with focal cerebral atrophy in the chronic phase
In cases of familial hemiplegic migraine or epilepsy, cerebral atrophy may occur at the site of focal symptoms. We report a case of sporadic hemiplegic migraine with marked cerebral atrophy 5 years after the initial diagnosis. The patient was a man in his 50s. The patient had a history of migraine w...
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Published in | Japanese Journal of Headache Vol. 50; no. 3; pp. 625 - 630 |
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Main Authors | , , , |
Format | Journal Article |
Language | Japanese |
Published |
The Japanese Headache Society
2024
一般社団法人 日本頭痛学会 |
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Online Access | Get full text |
ISSN | 1345-6547 2436-1577 |
DOI | 10.50860/jjho.50.3_625 |
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Abstract | In cases of familial hemiplegic migraine or epilepsy, cerebral atrophy may occur at the site of focal symptoms. We report a case of sporadic hemiplegic migraine with marked cerebral atrophy 5 years after the initial diagnosis. The patient was a man in his 50s. The patient had a history of migraine with aura. He was hospitalized three times in two years for migraines with focal symptoms such as aphasia, dyslexia, and visual field disturbances. On his first episode, he was diagnosed as transient ischemic attack and started taking Cilostazol, which seemed inappropriate retrospectively. On his second episode, he showed general convulsion and started taking an antiseizure medication. On his third episode, he was diagnosed with hemiplegic migraine with left hemiplegia and started taking other antiseizure medications with known preventive effects on migraine. Cerebral perfusion study showed hypoperfusion at the focus of cortical spreading depression during the first episode, whereas hyper-perfusion during the second and the third episode. Brain imaging 5 years after the first visit revealed marked brain atrophy on his right occipital lobe. He passed away when he drowned due to epileptic seizure while bathing. As the mechanism of the focal brain atrophy, neuronal damage due to (1) drastic changes in cerebral perfusion that appears during aura, (2) repetitive cortical spreading depression, and (3) coexistence of epilepsy, were suggested. The neuronal damage which we observed as FLAIR high lesion at the focus of cortical spreading depression is also described as cortical cytotoxic edema or cortical laminar necrosis. Regarding the possibly poor outcome of those hemiplegic migraine patients, recently approved promising agents such as anti-calcitonin-gene related peptide (CGRP) -related monoclonal antibodies or lasmiditan should have been considered. |
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AbstractList | In cases of familial hemiplegic migraine or epilepsy, cerebral atrophy may occur at the site of focal symptoms. We report a case of sporadic hemiplegic migraine with marked cerebral atrophy 5 years after the initial diagnosis. The patient was a man in his 50s. The patient had a history of migraine with aura. He was hospitalized three times in two years for migraines with focal symptoms such as aphasia, dyslexia, and visual field disturbances. On his first episode, he was diagnosed as transient ischemic attack and started taking Cilostazol, which seemed inappropriate retrospectively. On his second episode, he showed general convulsion and started taking an antiseizure medication. On his third episode, he was diagnosed with hemiplegic migraine with left hemiplegia and started taking other antiseizure medications with known preventive effects on migraine. Cerebral perfusion study showed hypoperfusion at the focus of cortical spreading depression during the first episode, whereas hyper-perfusion during the second and the third episode. Brain imaging 5 years after the first visit revealed marked brain atrophy on his right occipital lobe. He passed away when he drowned due to epileptic seizure while bathing. As the mechanism of the focal brain atrophy, neuronal damage due to (1) drastic changes in cerebral perfusion that appears during aura, (2) repetitive cortical spreading depression, and (3) coexistence of epilepsy, were suggested. The neuronal damage which we observed as FLAIR high lesion at the focus of cortical spreading depression is also described as cortical cytotoxic edema or cortical laminar necrosis. Regarding the possibly poor outcome of those hemiplegic migraine patients, recently approved promising agents such as anti-calcitonin-gene related peptide (CGRP) -related monoclonal antibodies or lasmiditan should have been considered. In cases of familial hemiplegic migraine or epilepsy, cerebral atrophy may occur at the site of focal symptoms. We report a case of sporadic hemiplegic migraine with marked cerebral atrophy 5 years after the initial diagnosis. The patient was a man in his 50s. The patient had a history of migraine with aura. He was hospitalized three times in two years for migraines with focal symptoms such as aphasia, dyslexia, and visual field disturbances. On his first episode, he was diagnosed as transient ischemic attack and started taking Cilostazol, which seemed inappropriate retrospectively. On his second episode, he showed general convulsion and started taking an antiseizure medication. On his third episode, he was diagnosed with hemiplegic migraine with left hemiplegia and started taking other antiseizure medications with known preventive effects on migraine. Cerebral perfusion study showed hypoperfusion at the focus of cortical spreading depression during the first episode, whereas hyper-perfusion during the second and the third episode. Brain imaging 5 years after the first visit revealed marked brain atrophy on his right occipital lobe. He passed away when he drowned due to epileptic seizure while bathing. As the mechanism of the focal brain atrophy, neuronal damage due to (1) drastic changes in cerebral perfusion that appears during aura, (2) repetitive cortical spreading depression, and (3) coexistence of epilepsy, were suggested. The neuronal damage which we observed as FLAIR high lesion at the focus of cortical spreading depression is also described as cortical cytotoxic edema or cortical laminar necrosis. Regarding the possibly poor outcome of those hemiplegic migraine patients, recently approved promising agents such as anti-calcitonin-gene related peptide (CGRP) -related monoclonal antibodies or lasmiditan should have been considered. 家族性片麻痺性片頭痛や,てんかんの症例では,巣症状の発生部位に一致して脳萎縮を呈することがある.われわれは,初診より7年の経過で著明な脳萎縮をきたした片頭痛の一例を経験したため,報告する.症例は50歳台の男性.前兆のある片頭痛の既往あり.失語,読字障害,視野障害などの巣症状を伴う片頭痛のため,当院に2年間で3回入院した.3回目の入院で左片麻痺を伴い,片麻痺性片頭痛疑いとした.初診時より7年後の頭部画像検査では,右後頭葉を中心に著明な脳萎縮を認めた.その機序として,①前兆期に出現する脳灌流の変化,②皮質拡延性抑制の反復,③痙攣の合併,などによる神経細胞障害が示唆された. |
Author | Kikuchi, Asami Arai, Naoyuki Kuroi, Yasuhiro Kubota, Yuichi |
Author_FL | 新井 直幸 久保田 有一 Kuroi Yasuhiro Kikuchi Asami |
Author_FL_xml | – sequence: 1 fullname: Kuroi Yasuhiro – sequence: 2 fullname: Kikuchi Asami – sequence: 3 fullname: 新井 直幸 – sequence: 4 fullname: 久保田 有一 |
Author_xml | – sequence: 1 fullname: Kuroi, Yasuhiro organization: Department of Spinal Neurosurgery, Tokyo Shinagawa Hospital – sequence: 1 fullname: Kikuchi, Asami organization: Department of Neurosurgery, Tokyo Women’s Medical University Adachi Medical Center – sequence: 1 fullname: Kubota, Yuichi organization: Department of Neurosurgery, Tokyo Women’s Medical University Adachi Medical Center – sequence: 1 fullname: Arai, Naoyuki organization: Department of Neurosurgery, Tokyo Women’s Medical University Adachi Medical Center |
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References | 8) 柴田 護 : 片頭痛治療におけるCGRP関連薬剤の意義.日本頭痛学会誌 48 : 515-519, 2022. 5) Iizuka T, Takahashi Y, Sato M, et al : Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation. J Neurol Neurosurg Psychiatry 83 : 205-212, 2012. 14) Ferrari MD, Klever RR, Terwindt GM, et al : Migraine pathophysiology: lessons from mouse models and human genetics. Lancet Neurol 14 : 65-80, 2015. 19) Hasırcı Bayır BR, Tutkavul K, Eser M, et al : Epilepsy in patients with familial hemiplegic migraine. Seizure 88 : 87-94, 2021. 12) Siskas N, Lefkopoulos A, Ioannidis I, et al : Cortical laminar necrosis in brain infarcts: serial MRI. Neuroradiology 45 : 283-288, 2003. 11) Labastida-Ramírez A, Rubio-Beltrán E, Haanes KA, et al : Lasmiditan inhibits calcitonin gene-related peptide release in the rodent trigeminovascular system. Pain 161 : 1092-1099, 2020. 18) Galovic M, van Dooren VQH, Postma TS, et al : Progressive Cortical Thinning in Patients With Focal Epilepsy. JAMA Neurol 76 : 1230-1239, 2019. 17) Gutschalk A, Kollmar R, Mohr A, et al : Multimodal functional imaging of prolonged neurological deficits in a patient suffering from familial hemiplegic migraine. Neurosci Lett 332 : 115-118, 2002. 1) 日本頭痛学会・国際頭痛分類委員会訳 : 国際頭痛分類第3版.医学書院,東京,2018. 10) Nelson DL, Phebus LA, Johnson KW, et al : Preclinical pharmacological profile of the selective 5-HT1F receptor agonist lasmiditan. Cephalalgia 10 : 1159-1169, 2010. 13) Arboix A, González-Peris S, Grivé E, et al : Cortical laminar necrosis related to migrainous cerebral infarction. World J Clin Cases 1 : 256-259, 2013. 7) Hu Y, Wang Z, Zhou L, et al : Prolonged Hemiplegic Migraine Led to Persistent Hyperperfusion and Cortical Necrosis: Case Report and Literature Review. Front Neurol 12 : 748034, 2021. 9) 頭痛の診療ガイドライン作成委員会 (編) : 頭痛の診療ガイドライン2021第1版, (日本神経学会・日本頭痛学会・日本神経治療学会監修) .医学書院,東京,2021, p146. 6) 津田正喜,加藤亜結美,渡辺圭介,ほか : ASLが診断に有用であった片麻痺性片頭痛の1例.臨床放射線 65 : 1143-1148, 2020. 16) Sadeghian H, Jafarian M, Karimzadeh F, et al : Neuronal death by repetitive cortical spreading depression in juvenile rat brain. Exp Neurol 233 : 438-446, 2012. 4) 飯塚 高浩 : MELASの脳卒中様発作の病態と治療.臨床神経 48 : 1006-1009, 2008. 20) Hayashi R, Tachikawa H, Watanabe R, et al : Familial hemiplegic migraine with irreversible brain damage. Intern Med 37 : 166-168, 1998. 3) 藤田 光 : Pro 頭痛のみを症候とするてんかん性頭痛は存在するか.日本頭痛学会誌49 : 168-171, 2022. 2) 榎日出夫 : てんかんと頭痛-migralepsyの再検証-.脳と発達 55 : 5-11, 2023. 15) Pelzer N, Hoogeveen ES, Ferrari MD, et al : Brain atrophy following hemiplegic migraine attacks. Cephalalgia 38 : 1199-1202, 2018. |
References_xml | – reference: 6) 津田正喜,加藤亜結美,渡辺圭介,ほか : ASLが診断に有用であった片麻痺性片頭痛の1例.臨床放射線 65 : 1143-1148, 2020. – reference: 5) Iizuka T, Takahashi Y, Sato M, et al : Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation. J Neurol Neurosurg Psychiatry 83 : 205-212, 2012. – reference: 9) 頭痛の診療ガイドライン作成委員会 (編) : 頭痛の診療ガイドライン2021第1版, (日本神経学会・日本頭痛学会・日本神経治療学会監修) .医学書院,東京,2021, p146. – reference: 18) Galovic M, van Dooren VQH, Postma TS, et al : Progressive Cortical Thinning in Patients With Focal Epilepsy. JAMA Neurol 76 : 1230-1239, 2019. – reference: 10) Nelson DL, Phebus LA, Johnson KW, et al : Preclinical pharmacological profile of the selective 5-HT1F receptor agonist lasmiditan. Cephalalgia 10 : 1159-1169, 2010. – reference: 14) Ferrari MD, Klever RR, Terwindt GM, et al : Migraine pathophysiology: lessons from mouse models and human genetics. Lancet Neurol 14 : 65-80, 2015. – reference: 7) Hu Y, Wang Z, Zhou L, et al : Prolonged Hemiplegic Migraine Led to Persistent Hyperperfusion and Cortical Necrosis: Case Report and Literature Review. Front Neurol 12 : 748034, 2021. – reference: 11) Labastida-Ramírez A, Rubio-Beltrán E, Haanes KA, et al : Lasmiditan inhibits calcitonin gene-related peptide release in the rodent trigeminovascular system. Pain 161 : 1092-1099, 2020. – reference: 8) 柴田 護 : 片頭痛治療におけるCGRP関連薬剤の意義.日本頭痛学会誌 48 : 515-519, 2022. – reference: 20) Hayashi R, Tachikawa H, Watanabe R, et al : Familial hemiplegic migraine with irreversible brain damage. Intern Med 37 : 166-168, 1998. – reference: 17) Gutschalk A, Kollmar R, Mohr A, et al : Multimodal functional imaging of prolonged neurological deficits in a patient suffering from familial hemiplegic migraine. Neurosci Lett 332 : 115-118, 2002. – reference: 2) 榎日出夫 : てんかんと頭痛-migralepsyの再検証-.脳と発達 55 : 5-11, 2023. – reference: 4) 飯塚 高浩 : MELASの脳卒中様発作の病態と治療.臨床神経 48 : 1006-1009, 2008. – reference: 3) 藤田 光 : Pro 頭痛のみを症候とするてんかん性頭痛は存在するか.日本頭痛学会誌49 : 168-171, 2022. – reference: 13) Arboix A, González-Peris S, Grivé E, et al : Cortical laminar necrosis related to migrainous cerebral infarction. World J Clin Cases 1 : 256-259, 2013. – reference: 19) Hasırcı Bayır BR, Tutkavul K, Eser M, et al : Epilepsy in patients with familial hemiplegic migraine. Seizure 88 : 87-94, 2021. – reference: 15) Pelzer N, Hoogeveen ES, Ferrari MD, et al : Brain atrophy following hemiplegic migraine attacks. Cephalalgia 38 : 1199-1202, 2018. – reference: 16) Sadeghian H, Jafarian M, Karimzadeh F, et al : Neuronal death by repetitive cortical spreading depression in juvenile rat brain. Exp Neurol 233 : 438-446, 2012. – reference: 1) 日本頭痛学会・国際頭痛分類委員会訳 : 国際頭痛分類第3版.医学書院,東京,2018. – reference: 12) Siskas N, Lefkopoulos A, Ioannidis I, et al : Cortical laminar necrosis in brain infarcts: serial MRI. Neuroradiology 45 : 283-288, 2003. |
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Snippet | In cases of familial hemiplegic migraine or epilepsy, cerebral atrophy may occur at the site of focal symptoms. We report a case of sporadic hemiplegic... In cases of familial hemiplegic migraine or epilepsy, cerebral atrophy may occur at the site of focal symptoms. We report a case of sporadic hemiplegic... |
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SubjectTerms | brain atrophy cortical spreading depression hemiplegic migraine 片麻痺性片頭痛 皮質拡延抑制 脳萎縮 |
Title | A case of hemiplegic migraine with focal cerebral atrophy in the chronic phase |
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