Pick's Disease Presenting as Tremulous Parkinsonism with Limited Levodopa Response-A Rare Cause of Corticobasal Syndrome.

IF 2.6 4区 医学 Q2 CLINICAL NEUROLOGY
Movement Disorders Clinical Practice Pub Date : 2024-08-01 Epub Date: 2024-06-03 DOI:10.1002/mdc3.14125
Shakya Bhattacharjee, William Scotton, Ibrahim Djoukhadar, Yvonne S Davidson, James Minshull, Andrew C Robinson, Federico Roncaroli, Christopher Kobylecki
{"title":"Pick's Disease Presenting as Tremulous Parkinsonism with Limited Levodopa Response-A Rare Cause of Corticobasal Syndrome.","authors":"Shakya Bhattacharjee, William Scotton, Ibrahim Djoukhadar, Yvonne S Davidson, James Minshull, Andrew C Robinson, Federico Roncaroli, Christopher Kobylecki","doi":"10.1002/mdc3.14125","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Corticobasal syndrome is a clinical diagnosis and common pathological causes are corticobasal degeneration, progressive supranuclear palsy and Alzheimer's disease.</p><p><strong>Objectives: </strong>We would like to highlight a rare but important differential of corticobasal syndrome.</p><p><strong>Methods: </strong>A 78-year-old female had a 4-year history of predominantly right-hand rest tremor, worsening of handwriting but no change in cognition. The clinical examination showed right upper limb postural and kinetic tremor, mild wrist rigidity and reduced amplitude of right-sided finger tapping. She was initially diagnosed as idiopathic Parkinson's disease. Five years after onset of symptoms, she demonstrated bilateral myoclonic jerks and right upper limb dystonic posturing. She could not copy movements with the right hand. The magnetic resonance imaging (MRI) revealed disproportionate atrophy in the parietal lobes bilaterally. The clinical diagnosis was changed to probable corticobasal syndrome. She passed away 11 years from onset of symptoms at the age of 85 years. She underwent a post-mortem.</p><p><strong>Results: </strong>The anterior and posterior frontal cortex, anterior cingulate, temporal neocortex, hippocampus and amygdaloid complex demonstrated considerable tau-related pathology consisting of a dense background of neuropil threads, and rounded, paranuclear neuronal inclusions consistent with Pick bodies. The immunostaining for three microtubule binding domain repeats (3R) tau performed on sections from the frontal and temporal lobes, basal ganglia and midbrain highlighted several inclusions whilst no 4R tau was observed. She was finally diagnosed with Pick's disease.</p><p><strong>Conclusions: </strong>Pick's disease can rarely present with clinical features of corticobasal syndrome.</p>","PeriodicalId":19029,"journal":{"name":"Movement Disorders Clinical Practice","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11329554/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Movement Disorders Clinical Practice","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/mdc3.14125","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/3 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Corticobasal syndrome is a clinical diagnosis and common pathological causes are corticobasal degeneration, progressive supranuclear palsy and Alzheimer's disease.

Objectives: We would like to highlight a rare but important differential of corticobasal syndrome.

Methods: A 78-year-old female had a 4-year history of predominantly right-hand rest tremor, worsening of handwriting but no change in cognition. The clinical examination showed right upper limb postural and kinetic tremor, mild wrist rigidity and reduced amplitude of right-sided finger tapping. She was initially diagnosed as idiopathic Parkinson's disease. Five years after onset of symptoms, she demonstrated bilateral myoclonic jerks and right upper limb dystonic posturing. She could not copy movements with the right hand. The magnetic resonance imaging (MRI) revealed disproportionate atrophy in the parietal lobes bilaterally. The clinical diagnosis was changed to probable corticobasal syndrome. She passed away 11 years from onset of symptoms at the age of 85 years. She underwent a post-mortem.

Results: The anterior and posterior frontal cortex, anterior cingulate, temporal neocortex, hippocampus and amygdaloid complex demonstrated considerable tau-related pathology consisting of a dense background of neuropil threads, and rounded, paranuclear neuronal inclusions consistent with Pick bodies. The immunostaining for three microtubule binding domain repeats (3R) tau performed on sections from the frontal and temporal lobes, basal ganglia and midbrain highlighted several inclusions whilst no 4R tau was observed. She was finally diagnosed with Pick's disease.

Conclusions: Pick's disease can rarely present with clinical features of corticobasal syndrome.

皮克病表现为左旋多巴反应受限的颤抖性帕金森症--皮质基底综合征的罕见病因
背景:皮质基底综合征是一种临床诊断,常见的病理原因是皮质基底变性、进行性核上性麻痹和阿尔茨海默病:我们希望强调皮质基底综合征的一种罕见但重要的鉴别方法:一名 78 岁的女性患者有 4 年的病史,主要表现为右手静止性震颤、书写能力恶化,但认知能力无变化。临床检查显示她右上肢姿势性和运动性震颤,手腕轻度僵硬,右侧手指敲击幅度减小。她最初被诊断为特发性帕金森病。发病五年后,她出现双侧肌阵挛抽搐和右上肢肌张力障碍姿势。她无法用右手模仿动作。磁共振成像(MRI)显示双侧顶叶不成比例地萎缩。临床诊断改为可能的皮质基底综合征。她在发病 11 年后去世,享年 85 岁。她接受了尸检:结果:额叶前部和后部皮层、扣带回前部、颞叶新皮层、海马体和杏仁核复合体显示出大量与 tau 相关的病理变化,包括密集的神经丝背景和与 Pick 体一致的圆形核旁神经元包涵体。在额叶和颞叶、基底节和中脑的切片上进行的3个微管结合域重复序列(3R)tau免疫染色突出显示了几个包涵体,但没有观察到4R tau。她最终被诊断为皮克病:结论:皮克氏病很少会出现皮质基底节综合征的临床特征。
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
CiteScore
4.00
自引率
7.50%
发文量
218
期刊介绍: Movement Disorders Clinical Practice- is an online-only journal committed to publishing high quality peer reviewed articles related to clinical aspects of movement disorders which broadly include phenomenology (interesting case/case series/rarities), investigative (for e.g- genetics, imaging), translational (phenotype-genotype or other) and treatment aspects (clinical guidelines, diagnostic and treatment algorithms)
×
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