Atypical Presentation of Amyloidosis in a Female Patient with Muscle Weakness.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Raziyeh Lashkari, Maryam Loghman, Leila Aghaghazvini, Hiva Saffar, Bentolhoda Ziaadini, Reza Shahriarirad, Mohammad Nekooeian, Mohammad Nejadhosseinian, Majid Alikhani
{"title":"Atypical Presentation of Amyloidosis in a Female Patient with Muscle Weakness.","authors":"Raziyeh Lashkari,&nbsp;Maryam Loghman,&nbsp;Leila Aghaghazvini,&nbsp;Hiva Saffar,&nbsp;Bentolhoda Ziaadini,&nbsp;Reza Shahriarirad,&nbsp;Mohammad Nekooeian,&nbsp;Mohammad Nejadhosseinian,&nbsp;Majid Alikhani","doi":"10.1155/2023/1553163","DOIUrl":null,"url":null,"abstract":"<p><p>Muscle involvement represents a well-recognized but rare manifestation of amyloidosis. Here, we report a 40-year-old female who presented with muscle weakness, musculoskeletal pain, and proteinuria, which was eventually diagnosed as myopathic amyloidosis based on muscle biopsy results. A multidisciplinary approach appears to be the cornerstone of the diagnostic work up for recognizing the unusual amyloid myopathy.</p>","PeriodicalId":9627,"journal":{"name":"Case Reports in Medicine","volume":"2023 ","pages":"1553163"},"PeriodicalIF":0.8000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118899/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2023/1553163","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Muscle involvement represents a well-recognized but rare manifestation of amyloidosis. Here, we report a 40-year-old female who presented with muscle weakness, musculoskeletal pain, and proteinuria, which was eventually diagnosed as myopathic amyloidosis based on muscle biopsy results. A multidisciplinary approach appears to be the cornerstone of the diagnostic work up for recognizing the unusual amyloid myopathy.

Abstract Image

Abstract Image

Abstract Image

女性肌无力患者淀粉样变性的不典型表现。
肌肉受累是淀粉样变的一种公认但罕见的表现。在这里,我们报告了一位40岁的女性,她表现为肌肉无力,肌肉骨骼疼痛和蛋白尿,最终根据肌肉活检结果诊断为肌病淀粉样变性。多学科方法似乎是诊断工作的基石,以识别不寻常的淀粉样肌病。
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 求助全文
来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信