Obelieniene Diana, Bauzaite Sandra, Kulakiene Ilona, Keleras Evaldas, Eitmonaite Indre, Rastenyte Daiva
Department of Neurology.
Department of Radiology.
Neuropsychiatr Dis Treat. 2018 Jan 4;14:179-184. doi: 10.2147/NDT.S146080. eCollection 2018.
Multiple system atrophy is a progressive neurodegenerative disorder that is characterized by autonomic failure, cerebellar ataxia and parkinsonism syndrome in various combinations. In spite of the presence of well-established clinical criteria for multiple system atrophy, ante-mortem diagnosis is difficult. In our case report, we present a 78-year-old female patient who presented with early progressive aphasia and severe autonomic dysfunction. Two years after appearance of the first symptoms, she fulfilled all the major criteria for probable multiple system atrophy with rapid progression. In addition, brain magnetic resonance imaging and fluorodeoxyglucose-positron emission tomography findings were more typical for progressive supranuclear palsy. Clinically differentiating multiple system atrophy from progressive supranuclear palsy and other similar neurodegenerative disorders may be challenging in all stages of the disease, especially with atypical disease presentation.
多系统萎缩是一种进行性神经退行性疾病,其特征是自主神经功能衰竭、小脑共济失调和帕金森综合征以各种组合形式出现。尽管有多系统萎缩公认的临床标准,但生前诊断仍很困难。在我们的病例报告中,我们介绍了一名78岁女性患者,她出现了早期进行性失语和严重的自主神经功能障碍。在出现首发症状两年后,她符合可能的多系统萎缩的所有主要标准且进展迅速。此外,脑磁共振成像和氟脱氧葡萄糖-正电子发射断层扫描结果在进行性核上性麻痹中更具典型性。在疾病的所有阶段,临床上区分多系统萎缩与进行性核上性麻痹及其他类似的神经退行性疾病可能具有挑战性,尤其是在疾病表现不典型时。