Bersano Enrica, Sarnelli Maria Francesca, Solara Valentina, De Marchi Fabiola, Sacchetti Gian Mauro, Stecco Alessandro, Corrado Lucia, D'alfonso Sandra, Cantello Roberto, Mazzini Letizia
a Department of Neurology , Eastern Piedmont University, "Maggiore della Carità" University Hospital , Novara , Italy.
b ALS Center, Department of Neurology , "Maggiore della Carità" University Hospital , Novara , Italy.
Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):463-465. doi: 10.1080/21678421.2018.1440405. Epub 2018 Feb 16.
We describe a 64-year-old woman, suffering from late-onset obsessive-compulsive disorder (OCD) from the age of 57, who developed dysarthria and dysphagia, spastic diplegic, and proximal muscles weakness. Needle electromyography showed no active denervation. Neuropsychological evaluation showed intact cognitive functioning. We diagnosed upper motor neuron disease (MND), with no known genetic correlates. Brain magnetic resonance (MRI) detected bilateral hippocampal atrophy with sclerosis of right hippocampus. 18F-FDG positron emission tomography (PET) showed moderate right temporal cortex thinning. Six months later, motor and behavioral symptoms worsened. Neuropsychological examination revealed long-term memory deficit and executive dysfunction. MRI and PET evidenced severe worsening of atrophy in temporal and frontal lobes. Four years later a definitive diagnosis of primary lateral sclerosis (PLS) and FTD was made. To our knowledge, this is the first report of PLS and FTD with OCD at onset.
我们描述了一名64岁女性,她从57岁起患有迟发性强迫症(OCD),出现了构音障碍和吞咽困难、痉挛性双侧瘫以及近端肌肉无力。针极肌电图显示无活动性失神经。神经心理学评估显示认知功能完好。我们诊断为上运动神经元病(MND),无已知的遗传相关性。脑磁共振成像(MRI)检测到双侧海马萎缩,右侧海马硬化。18F-氟代脱氧葡萄糖正电子发射断层扫描(PET)显示右侧颞叶皮质中度变薄。6个月后,运动和行为症状恶化。神经心理学检查显示长期记忆缺陷和执行功能障碍。MRI和PET证明颞叶和额叶萎缩严重恶化。4年后确诊为原发性侧索硬化症(PLS)和额颞叶痴呆(FTD)。据我们所知,这是首例起病时伴有强迫症的PLS和FTD报告。