Diagnostic Criteria for Moyamoya Disease - 2021 Revised Version
In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in the new "Diagnostic Criteria 2021" for moyamoya disease and its scientific basis to make it widely known to the world. The revised criteria cove...
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Published in | Neurologia Medico-Chirurgica Vol. 62; no. 7; pp. 307 - 312 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Japan
The Japan Neurosurgical Society
15.07.2022
THE JAPAN NEUROSURGICAL SOCIETY Japan Science and Technology Agency |
Subjects | |
Online Access | Get full text |
ISSN | 0470-8105 1349-8029 |
DOI | 10.2176/jns-nmc.2022-0072 |
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Abstract | In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in the new "Diagnostic Criteria 2021" for moyamoya disease and its scientific basis to make it widely known to the world. The revised criteria cover all aspects of the disease, including a definition of the disease concept, diagnostic imaging, and the concept of quasi-moyamoya disease (moyamoya syndrome). |
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AbstractList | In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in the new “Diagnostic Criteria 2021” for moyamoya disease and its scientific basis to make it widely known to the world. The revised criteria cover all aspects of the disease, including a definition of the disease concept, diagnostic imaging, and the concept of quasi-moyamoya disease (moyamoya syndrome). [Abstract] In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in the new "Diagnostic Criteria 2021" for moyamoya disease and its scientific basis to make it widely known to the world. The revised criteria cover all aspects of the disease, including a definition of the disease concept, diagnostic imaging, and the concept of quasi-moyamoya disease (moyamoya syndrome). |
ArticleNumber | 2022-0072 |
Author | KURODA, Satoshi IWAMA, Toru TOMINAGA, Teiji TAKAHASHI, Jun FUJIMURA, Miki The Research Committee on Moyamoya Disease (Spontaneous Occlusion of Circle of Willis) of the Ministry of Health, Labor, and Welfare, Japan KATAOKA, Hiroharu OGASAWARA, Kuniaki MIYAMOTO, Susumu |
Author_xml | – sequence: 1 fullname: FUJIMURA, Miki organization: Department of Neurosurgery, Hokkaido University Graduate School of Medicine – sequence: 1 fullname: OGASAWARA, Kuniaki organization: Department of Neurosurgery, Iwate Medical University – sequence: 1 fullname: TOMINAGA, Teiji organization: Department of Neurosurgery, Tohoku University Graduate School of Medicine – sequence: 1 fullname: The Research Committee on Moyamoya Disease (Spontaneous Occlusion of Circle of Willis) of the Ministry of Health, Labor, and Welfare, Japan – sequence: 1 fullname: KURODA, Satoshi organization: Department of Neurosurgery, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama – sequence: 1 fullname: TAKAHASHI, Jun organization: Department of Neurosurgery, Kindai University Faculty of Medicine – sequence: 1 fullname: KATAOKA, Hiroharu organization: Department of Neurosurgery, National Cerebral and Cardiovascular Center – sequence: 1 fullname: IWAMA, Toru organization: Department of Neurosurgery, Gifu University School of Medicine – sequence: 1 fullname: MIYAMOTO, Susumu organization: Department of Neurosurgery, Kyoto University Graduate School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35613882$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.2176/nmc.oa.2017-0198 10.2176/nmc.oa.2015-0044 10.1227/NEU.0000000000001201 10.3171/2008.9.JNS17658 10.2335/scs.46.1 10.1016/S0387-7604(79)80022-4 10.1161/STROKEAHA.110.608471 10.1161/STROKEAHA.114.004761 10.1016/S1474-4422(08)70240-0 10.1530/eje.1.01809 10.1016/j.wneu.2018.10.001 10.2176/nmc.50.378 10.1016/S0303-8467(97)00082-6 10.1001/archneur.1969.00480090076012 10.1507/endocrj1954.16.665 10.1016/j.neulet.2014.10.021 10.1038/jhg.2010.132 10.1161/STROKEAHA.111.622522 10.1159/000352065 10.1161/01.STR.0000182256.32489.99 10.2176/nmc.52.245 10.1371/journal.pone.0022542 10.1007/s00701-012-1472-4 10.1016/j.wneu.2019.02.120 |
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Copyright | 2022 The Japan Neurosurgical Society 2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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CorporateAuthor | Graduate School of Medicine and Pharmaceutical Sciences Gifu University School of Medicine Department of Neurosurgery Hokkaido University Graduate School of Medicine Iwate Medical University Kyoto University Graduate School of Medicine Kindai University Faculty of Medicine National Cerebral and Cardiovascular Center University of Toyama Tohoku University Graduate School of Medicine The Research Committee on Moyamoya Disease (Spontaneous Occlusion of Circle of Willis) of the Ministry of Health, Labor, and Welfare, Japan Research Committee on Moyamoya Disease (Spontaneous Occlusion of Circle of Willis) of the Ministry of Health, Labor, and Welfare, Japan |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 e-mail: skuroda@med.u-toyama.ac.jp Corresponding author: Satoshi Kuroda, MD, PhD Department of Neurosurgery, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan. |
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References | 17) Kuroda S, Kashiwazaki D, Akioka N, et al.: Specific shrinkage of carotid forks in moyamoya disease: a novel key finding for diagnosis. Neurol Med Chir (Tokyo) 55: 796-804, 2015 11) Kuroda S, Ishikawa T, Houkin K, Nanba R, Hokari M, Iwasaki Y: Incidence and clinical features of disease progression in adult moyamoya disease. Stroke 36: 2148-2153, 2005 9) Liu W, Morito D, Takashima S, et al.: Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development. PloS One 6: e22542, 2011 15) Mineharu Y, Takagi Y, Koizumi A, et al.: Genetic and nongenetic factors for contralateral progression of unilateral moyamoya disease: the first report from the SUPRA Japan Study Group. J Neurosurg 1: 1-10, 2021 2) Kudo T: Occlusion of the circle of Willis with special reference to its developmental process. No To Shinkei 18: 889-896, 1966 22) Komotar RJ, Starke RM, Otten ML, et al.: The role of indirect extracranial-intracranial bypass in the treatment of symptomatic intracranial atheroocclusive disease. J Neurosurg 110: 896-904, 2009 5) Kuroda S, Houkin K: Moyamoya disease: current concepts and future perspectives. Lancet Neurol 7: 1056-1066, 2008 14) Hayashi K, Suyama K, Nagata I: Clinical features of unilateral moyamoya disease. Neurol Med Chir (Tokyo) 50: 378-385, 2010 28) Fernandez-Alvarez E, Pineda M, Royo C, Manzanares R: "Moya-moya" disease caused by cranial trauma. Brain Dev 1: 133-138, 1979 6) Fukui M: Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ( 'moyamoya' disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg 99: S238-240, 1997 27) Ahn JH, Jeon JP, Kim JE, et al.: Association of hyperthyroidism and thyroid autoantibodies with moyamoya disease and its stroke event: a population-based case-control study and meta-analysis. Neurol Med Chir (Tokyo) 58: 116-123, 2018 18) Yamamoto S, Kashiwazaki D, Akioka N, Kuwayama N, Noguchi K, Kuroda S: Progressive shrinkage of involved arteries in parallel with disease progression in moyamoya disease. World Neurosurg 122: e253-e261, 2019 23) Uchino H, Kim JH, Fujima N, et al.: Synergistic interactions between direct and indirect bypasses in combined procedures: the significance of indirect bypasses in moyamoya disease. Neurosurgery 80: 201-209, 2017 4) Suzuki J, Takaku A: Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol 20: 288-299, 1969 13) Yeon JY, Shin HJ, Kong DS, et al.: The prediction of contralateral progression in children and adolescents with unilateral moyamoya disease. Stroke 42: 2973-2976, 2011 25) Biondi B, Palmieri EA, Klain M, Schlumberger M, Filetti S, Lombardi G: Subclinical hyperthyroidism: clinical features and treatment options. Eur J Endocrinol 152: 1-9, 2005 20) Ryoo S, Cha J, Kim SJ, et al.: High-resolution magnetic resonance wall imaging findings of Moyamoya disease. Stroke 45: 2457-2460, 2014 7) Hashimoto N, Tominaga T, Miyamoto S, et al.: Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis; Health Labour Sciences Research Grant for Research on Measures for Infractable Diseases. Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis). Neurol Med Chir (Tokyo) 52: 245-266, 2012 24) Maruchi N, Furihata R, Makiuchi M: Epidemiological studies on hyperthyroidism. Endocrinol Jpn 16: 665-672, 1969 16) Kaku Y, Morioka M, Ohmori Y, et al.: Outer-diameter narrowing of the internal carotid and middle cerebral arteries in moyamoya disease detected on 3D constructive interference in steady-state MR image: is arterial constrictive remodeling a major pathogenesis? Acta Neurochir (Wien) 154: 2151-2157, 2012 21) Yuan M, Liu ZQ, Wang ZQ, Li B, Xu LJ, Xiao XL: High-resolution MR imaging of the arterial wall in moyamoya disease. Neurosci Lett 584: 77-82, 2015 19) Yamamoto S, Kashiwazaki D, Uchino H, et al.: Stenosis severity-dependent shrinkage of posterior cerebral artery in moyamoya disease. World Neurosurg 126: e661-e670, 2019 26) Li H, Zhang ZS, Dong ZN, et al.: Increased thyroid function and elevated thyroid autoantibodies in pediatric patients with moyamoya disease: a case-control study. Stroke 42: 1138-1139, 2011 8) Tominaga T, Suzuki N, Miyamoto S, et al.: Recommendations for the management of moyamoya disease: a statement from Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) [2nd Edition]. Surg Cereb Stroke 46: 1-24, 2018 1) Takeuchi K, Shimizu K: Hypoplasia of the bilateral internal carotid arteries. No To Shinkei 9: 37-43, 1957 29) Zaletel M, Surlan-Popovic K, Pretnar-Oblak J, Zvan B: Moyamoya syndrome with arteriovenous dural fistula after head trauma. Acta Clin Croat 50: 115-120, 2011 10) Kamada F, Aoki Y, Narisawa A, et al.: A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. J Hum Genet 56: 34-40, 2011 12) Mineharu Y, Takagi Y, Takahashi JC, et al.: Rapid progression of unilateral moyamoya disease in a patient with a family history and an RNF213 risk variant. Cerebrovasc Dis 36: 155-157, 2013 3) Nishimoto A, Sugiu R, Takeuchi S: Hemangiomatous malformation of bilateral internal carotid artery at the base of brain. Brain Nerve (Tokyo) 17: 750-752, 1966 22 23 24 25 26 27 28 29 10 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 21 |
References_xml | – reference: 7) Hashimoto N, Tominaga T, Miyamoto S, et al.: Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis; Health Labour Sciences Research Grant for Research on Measures for Infractable Diseases. Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis). Neurol Med Chir (Tokyo) 52: 245-266, 2012 – reference: 11) Kuroda S, Ishikawa T, Houkin K, Nanba R, Hokari M, Iwasaki Y: Incidence and clinical features of disease progression in adult moyamoya disease. Stroke 36: 2148-2153, 2005 – reference: 12) Mineharu Y, Takagi Y, Takahashi JC, et al.: Rapid progression of unilateral moyamoya disease in a patient with a family history and an RNF213 risk variant. Cerebrovasc Dis 36: 155-157, 2013 – reference: 5) Kuroda S, Houkin K: Moyamoya disease: current concepts and future perspectives. Lancet Neurol 7: 1056-1066, 2008 – reference: 21) Yuan M, Liu ZQ, Wang ZQ, Li B, Xu LJ, Xiao XL: High-resolution MR imaging of the arterial wall in moyamoya disease. Neurosci Lett 584: 77-82, 2015 – reference: 29) Zaletel M, Surlan-Popovic K, Pretnar-Oblak J, Zvan B: Moyamoya syndrome with arteriovenous dural fistula after head trauma. Acta Clin Croat 50: 115-120, 2011 – reference: 20) Ryoo S, Cha J, Kim SJ, et al.: High-resolution magnetic resonance wall imaging findings of Moyamoya disease. Stroke 45: 2457-2460, 2014 – reference: 2) Kudo T: Occlusion of the circle of Willis with special reference to its developmental process. No To Shinkei 18: 889-896, 1966 – reference: 9) Liu W, Morito D, Takashima S, et al.: Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development. PloS One 6: e22542, 2011 – reference: 13) Yeon JY, Shin HJ, Kong DS, et al.: The prediction of contralateral progression in children and adolescents with unilateral moyamoya disease. Stroke 42: 2973-2976, 2011 – reference: 24) Maruchi N, Furihata R, Makiuchi M: Epidemiological studies on hyperthyroidism. Endocrinol Jpn 16: 665-672, 1969 – reference: 1) Takeuchi K, Shimizu K: Hypoplasia of the bilateral internal carotid arteries. No To Shinkei 9: 37-43, 1957 – reference: 25) Biondi B, Palmieri EA, Klain M, Schlumberger M, Filetti S, Lombardi G: Subclinical hyperthyroidism: clinical features and treatment options. Eur J Endocrinol 152: 1-9, 2005 – reference: 4) Suzuki J, Takaku A: Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol 20: 288-299, 1969 – reference: 18) Yamamoto S, Kashiwazaki D, Akioka N, Kuwayama N, Noguchi K, Kuroda S: Progressive shrinkage of involved arteries in parallel with disease progression in moyamoya disease. World Neurosurg 122: e253-e261, 2019 – reference: 3) Nishimoto A, Sugiu R, Takeuchi S: Hemangiomatous malformation of bilateral internal carotid artery at the base of brain. Brain Nerve (Tokyo) 17: 750-752, 1966 – reference: 27) Ahn JH, Jeon JP, Kim JE, et al.: Association of hyperthyroidism and thyroid autoantibodies with moyamoya disease and its stroke event: a population-based case-control study and meta-analysis. Neurol Med Chir (Tokyo) 58: 116-123, 2018 – reference: 19) Yamamoto S, Kashiwazaki D, Uchino H, et al.: Stenosis severity-dependent shrinkage of posterior cerebral artery in moyamoya disease. World Neurosurg 126: e661-e670, 2019 – reference: 6) Fukui M: Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ( 'moyamoya' disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg 99: S238-240, 1997 – reference: 10) Kamada F, Aoki Y, Narisawa A, et al.: A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. J Hum Genet 56: 34-40, 2011 – reference: 23) Uchino H, Kim JH, Fujima N, et al.: Synergistic interactions between direct and indirect bypasses in combined procedures: the significance of indirect bypasses in moyamoya disease. Neurosurgery 80: 201-209, 2017 – reference: 15) Mineharu Y, Takagi Y, Koizumi A, et al.: Genetic and nongenetic factors for contralateral progression of unilateral moyamoya disease: the first report from the SUPRA Japan Study Group. J Neurosurg 1: 1-10, 2021 – reference: 17) Kuroda S, Kashiwazaki D, Akioka N, et al.: Specific shrinkage of carotid forks in moyamoya disease: a novel key finding for diagnosis. Neurol Med Chir (Tokyo) 55: 796-804, 2015 – reference: 16) Kaku Y, Morioka M, Ohmori Y, et al.: Outer-diameter narrowing of the internal carotid and middle cerebral arteries in moyamoya disease detected on 3D constructive interference in steady-state MR image: is arterial constrictive remodeling a major pathogenesis? Acta Neurochir (Wien) 154: 2151-2157, 2012 – reference: 22) Komotar RJ, Starke RM, Otten ML, et al.: The role of indirect extracranial-intracranial bypass in the treatment of symptomatic intracranial atheroocclusive disease. J Neurosurg 110: 896-904, 2009 – reference: 8) Tominaga T, Suzuki N, Miyamoto S, et al.: Recommendations for the management of moyamoya disease: a statement from Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) [2nd Edition]. Surg Cereb Stroke 46: 1-24, 2018 – reference: 26) Li H, Zhang ZS, Dong ZN, et al.: Increased thyroid function and elevated thyroid autoantibodies in pediatric patients with moyamoya disease: a case-control study. Stroke 42: 1138-1139, 2011 – reference: 28) Fernandez-Alvarez E, Pineda M, Royo C, Manzanares R: "Moya-moya" disease caused by cranial trauma. Brain Dev 1: 133-138, 1979 – reference: 14) Hayashi K, Suyama K, Nagata I: Clinical features of unilateral moyamoya disease. Neurol Med Chir (Tokyo) 50: 378-385, 2010 – ident: 2 – ident: 27 doi: 10.2176/nmc.oa.2017-0198 – ident: 17 doi: 10.2176/nmc.oa.2015-0044 – ident: 23 doi: 10.1227/NEU.0000000000001201 – ident: 22 doi: 10.3171/2008.9.JNS17658 – ident: 8 doi: 10.2335/scs.46.1 – ident: 28 doi: 10.1016/S0387-7604(79)80022-4 – ident: 26 doi: 10.1161/STROKEAHA.110.608471 – ident: 20 doi: 10.1161/STROKEAHA.114.004761 – ident: 5 doi: 10.1016/S1474-4422(08)70240-0 – ident: 25 doi: 10.1530/eje.1.01809 – ident: 18 doi: 10.1016/j.wneu.2018.10.001 – ident: 14 doi: 10.2176/nmc.50.378 – ident: 3 – ident: 6 doi: 10.1016/S0303-8467(97)00082-6 – ident: 4 doi: 10.1001/archneur.1969.00480090076012 – ident: 24 doi: 10.1507/endocrj1954.16.665 – ident: 1 – ident: 21 doi: 10.1016/j.neulet.2014.10.021 – ident: 10 doi: 10.1038/jhg.2010.132 – ident: 15 – ident: 13 doi: 10.1161/STROKEAHA.111.622522 – ident: 29 – ident: 12 doi: 10.1159/000352065 – ident: 11 doi: 10.1161/01.STR.0000182256.32489.99 – ident: 7 doi: 10.2176/nmc.52.245 – ident: 9 doi: 10.1371/journal.pone.0022542 – ident: 16 doi: 10.1007/s00701-012-1472-4 – ident: 19 doi: 10.1016/j.wneu.2019.02.120 |
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Snippet | In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in the new... [Abstract] In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in... |
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Title | Diagnostic Criteria for Moyamoya Disease - 2021 Revised Version |
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