Department of Neurology, Manchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust (Salford Royal Hospital), Salford, UK.
Department of Neurology, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Mov Disord Clin Pract. 2024 Aug;11(8):1025-1029. doi: 10.1002/mdc3.14125. Epub 2024 Jun 3.
Corticobasal syndrome is a clinical diagnosis and common pathological causes are corticobasal degeneration, progressive supranuclear palsy and Alzheimer's disease.
We would like to highlight a rare but important differential of corticobasal syndrome.
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.
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.
Pick's disease can rarely present with clinical features of corticobasal syndrome.
皮质基底节综合征是一种临床诊断,常见的病理原因包括皮质基底节变性、进行性核上性麻痹和阿尔茨海默病。
我们想强调皮质基底节综合征的一个罕见但重要的鉴别诊断。
一位 78 岁女性,主要表现为右手静止性震颤,书写困难逐渐加重,但认知功能无变化,病史已有 4 年。临床检查显示右侧上肢姿势性和运动性震颤,轻度腕部僵硬,右侧手指叩击幅度减小。最初诊断为特发性帕金森病。发病 5 年后,她出现双侧肌阵挛性抽搐和右侧上肢扭转性姿势。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萎缩。临床诊断更改为可能的皮质基底节综合征。她在发病 11 年后,即 85 岁时去世。进行了尸检。
额、前扣带回、颞叶新皮质、海马和杏仁核复合体表现出大量与 tau 相关的病理学改变,包括神经丝的密集背景和与 Pick 体一致的圆形、核旁神经元包涵体。对来自额叶和颞叶、基底节和中脑的切片进行 3R 微管结合域重复 tau 的免疫染色,突出了几个包涵体,而未观察到 4R tau。她最终被诊断为 Pick 病。
Pick 病罕见地以皮质基底节综合征的临床特征表现出来。