异ferlin病的磁共振成像模式变异性。

Q3 Medicine Acta Myologica Pub Date : 2021-12-31 eCollection Date: 2021-12-01 DOI:10.36185/2532-1900-059
Sergey N Bardakov, Vadim A Tsargush, Pierre G Carlier, Sergey S Nikitin, Sergey A Kurbatov, Angelina A Titova, Zoya R Umakhanova, Patimat G Akhmedova, Raisat M Magomedova, Igor S Zheleznyak, Alexander A Emelyantsev, Ekaterina N Berezhnaya, Ivan A Yakovlev, Artur A Isaev, Roman V Deev
{"title":"异ferlin病的磁共振成像模式变异性。","authors":"Sergey N Bardakov,&nbsp;Vadim A Tsargush,&nbsp;Pierre G Carlier,&nbsp;Sergey S Nikitin,&nbsp;Sergey A Kurbatov,&nbsp;Angelina A Titova,&nbsp;Zoya R Umakhanova,&nbsp;Patimat G Akhmedova,&nbsp;Raisat M Magomedova,&nbsp;Igor S Zheleznyak,&nbsp;Alexander A Emelyantsev,&nbsp;Ekaterina N Berezhnaya,&nbsp;Ivan A Yakovlev,&nbsp;Artur A Isaev,&nbsp;Roman V Deev","doi":"10.36185/2532-1900-059","DOIUrl":null,"url":null,"abstract":"<p><p>The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy.</p><p><strong>Materials and methods: </strong>Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.</p><p><strong>Results: </strong>Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.</p><p><strong>Conclusions: </strong>Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.</p>","PeriodicalId":35953,"journal":{"name":"Acta Myologica","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/bb/d9/am-2021-04-158.PMC8744010.pdf","citationCount":"3","resultStr":"{\"title\":\"Magnetic resonance imaging pattern variability in dysferlinopathy.\",\"authors\":\"Sergey N Bardakov,&nbsp;Vadim A Tsargush,&nbsp;Pierre G Carlier,&nbsp;Sergey S Nikitin,&nbsp;Sergey A Kurbatov,&nbsp;Angelina A Titova,&nbsp;Zoya R Umakhanova,&nbsp;Patimat G Akhmedova,&nbsp;Raisat M Magomedova,&nbsp;Igor S Zheleznyak,&nbsp;Alexander A Emelyantsev,&nbsp;Ekaterina N Berezhnaya,&nbsp;Ivan A Yakovlev,&nbsp;Artur A Isaev,&nbsp;Roman V Deev\",\"doi\":\"10.36185/2532-1900-059\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy.</p><p><strong>Materials and methods: </strong>Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.</p><p><strong>Results: </strong>Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.</p><p><strong>Conclusions: </strong>Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.</p>\",\"PeriodicalId\":35953,\"journal\":{\"name\":\"Acta Myologica\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/bb/d9/am-2021-04-158.PMC8744010.pdf\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Myologica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36185/2532-1900-059\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/12/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Myologica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36185/2532-1900-059","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/12/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 3

摘要

磁共振成像(MRI)在肌病诊断中的广泛应用,使其有可能澄清异常肌病的典型MRI模式。然而,对异铁鞘病MRI表现的可变性并没有给予足够的重视。材料与方法:对25例有异ferlinopathy临床表现的患者进行检查。对所有患者,测量肌酸磷酸激酶水平并检查分子遗传学。2例患者行肌肉活检免疫组化检查。MRI扫描包括T2多层多回波、T1加权、T2加权和短Tau反转恢复T2加权序列。对脂肪替代和肌肉肿胀进行定量和半定量评价。结果:MRI模式的可变性在骨盆和腿部肌肉中最低,在大腿肌肉中最高。三种主要的MRI模式被区分开来:后显性(80%),前显性(16%)和弥漫性(4%)。在前显性型患者中,胶原样变异(4%)、近端变异(4%)和假性肌炎(8%)分别被区分。结论:了解异ferlinopathy的非典型MRI模式对于提高常规诊断效率和优化致病基因突变的搜索是重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Magnetic resonance imaging pattern variability in dysferlinopathy.

The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in dysferlinopathy.

Materials and methods: Twenty-five patients with the clinical manifestations of dysferlinopathy were examined. For all patients, creatine phosphokinase levels were measured and molecular genetics were examined. In two patients, immunohistochemical examinations of muscle biopsies were performed. MRI scanning was included T2 multi-slice multi-echo, T1 weighted, T2 weighted and Short Tau Inversion Recovery T2 weighted sequences. Quantitative and semi-quantitative evaluations of fatty replacement and swelling of the muscles were undertaken.

Results: Variability in the MRI patterns was lowest in the pelvis and leg muscles and highest in the thigh muscles. Three main types of MRI patterns were distinguished: posterior-dominant (80%), anterior-dominant (16%), and diffuse (4%). Among patients with the anterior-dominant pattern, the collagen-like variant (4%), proximal variant (4%) and pseudo-myositis (8%) were separately distinguished.

Conclusions: Awareness of atypical MRI patterns in dysferlinopathy is important for increasing the efficiency of routine diagnostics and optimizing the search for causative gene mutations.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
发文量
0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
×
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