Familial hemiplegic migraine in developmental age: report of two cases.

D Lendvai, F Monteleone, G Melpignano, E Turri, P Verdecchia, A Cantani
{"title":"Familial hemiplegic migraine in developmental age: report of two cases.","authors":"D Lendvai,&nbsp;F Monteleone,&nbsp;G Melpignano,&nbsp;E Turri,&nbsp;P Verdecchia,&nbsp;A Cantani","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The authors report two cases of a particular type of migraine with aura, known as familial hemiplegic migraine (FHM). According to the International Headache Society (IHS) diagnostic criteria, the FHM can be diagnosed with the exception of organic causes, in a patient with migraine with aura including emiparesis of anything severity and with an end occurring a member of the family with similarity in the attach pattern. The two clinical cases reported clearly show these features and they can be considered exemplary for this type of pathology. This rare type of migraine has an unknown etiology, it seems to depend on a decreases of cerebral blood flow originative on the occipital lobe, over the subsequentially spreading anteriory region temporal and parietal lobe. The hypoperfusion with the next following neural ischemia is related to the variation of blood flow and/or \"the spreading depression\" supported by Leao and Olesen recently. We wanted to show these two cases so that the psychiatrist, the pediatrician, and the neurologist can be able to refer parents to the right approach, considering possibility of a pathology rare but benign; this is the FHM.</p>","PeriodicalId":21382,"journal":{"name":"Rivista europea per le scienze mediche e farmacologiche = European review for medical and pharmacological sciences = Revue europeenne pour les sciences medicales et pharmacologiques","volume":"18 4","pages":"143-7"},"PeriodicalIF":0.0000,"publicationDate":"1996-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rivista europea per le scienze mediche e farmacologiche = European review for medical and pharmacological sciences = Revue europeenne pour les sciences medicales et pharmacologiques","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The authors report two cases of a particular type of migraine with aura, known as familial hemiplegic migraine (FHM). According to the International Headache Society (IHS) diagnostic criteria, the FHM can be diagnosed with the exception of organic causes, in a patient with migraine with aura including emiparesis of anything severity and with an end occurring a member of the family with similarity in the attach pattern. The two clinical cases reported clearly show these features and they can be considered exemplary for this type of pathology. This rare type of migraine has an unknown etiology, it seems to depend on a decreases of cerebral blood flow originative on the occipital lobe, over the subsequentially spreading anteriory region temporal and parietal lobe. The hypoperfusion with the next following neural ischemia is related to the variation of blood flow and/or "the spreading depression" supported by Leao and Olesen recently. We wanted to show these two cases so that the psychiatrist, the pediatrician, and the neurologist can be able to refer parents to the right approach, considering possibility of a pathology rare but benign; this is the FHM.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
发育期家族性偏瘫性偏头痛2例报告。
作者报告了两例特殊类型的先兆偏头痛,被称为家族偏瘫偏头痛(FHM)。根据国际头痛协会(IHS)的诊断标准,除了器质性原因外,FHM可以被诊断为偏头痛的先兆患者,包括任何严重的癫痫发作,并且最终发生的家庭成员具有相似的附加模式。报告的两个临床病例清楚地显示了这些特征,他们可以被认为是这种类型病理的典范。这种罕见类型的偏头痛病因不明,似乎是由于源自枕叶的脑血流量减少,继而扩散到颞叶和顶叶前区。神经缺血后的灌注不足与血流变化和/或Leao和Olesen最近支持的“扩散性抑郁”有关。我们想展示这两个病例,这样精神科医生、儿科医生和神经科医生就能向家长推荐正确的方法,考虑到这种罕见但良性的病理的可能性;这是FHM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The mouth-stomach crossing of Helicobacter pylori. HCV and dermatomyositis: report of 5 cases of dermatomyositis in patients with HCV infection. Effective treatment of osteoarthritis with a 150 mg prolonged-release of diclofenac sodium. Toxoplasmosis in pregnancy: research on 2295 women in Rome and its province. Transcranial Doppler validation of hemodynamic vertebrobasilar insufficiency diagnosis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1