Rocha Ana Luísa, Costa Andreia, Garrett Maria Carolina, Meireles Joana
Department of Neurology, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Department of Neurology, Centro Hospitalar do Tâmega e Sousa, Penafiel, Portugal.
BMJ Case Rep. 2018 Dec 13;11(1):e226664. doi: 10.1136/bcr-2018-226664.
Less than 10% of Alzheimer's disease (AD) cases are familial. Presenilin-1 (PSEN1) mutations are the most frequent aetiology and may be associated to atypical neurological manifestations. We report the case of a 27-year-old right-handed man, ensuing with mild cognitive impairment, motor discoordination and axial myoclonus after a parachute accident. At age 32 he was referred to our neurology clinic, presenting cognitive impairment, cerebellar syndrome, axial myoclonus and hypomimia, without other signs of parkinsonism. Because of absence of family history, he was worked up along the line of spinal ataxic disorders. Later, he developed pseudobulbar affect, cognitive deterioration, right upper limb paresis and spastic paraparesis. Subsequent investigation identified a PSEN1 P117L mutation and the diagnosis of autosomal dominant AD was made. This case illustrates the diagnostic challenge imposed by atypical presentation of de novo PSEN1 mutation, leading to unnecessary investigation. Genetic study might be essential for defining the diagnosis.
不到10%的阿尔茨海默病(AD)病例为家族性。早老素-1(PSEN1)突变是最常见的病因,可能与非典型神经表现有关。我们报告一例27岁右利手男性病例,该患者在一次跳伞事故后出现轻度认知障碍、运动不协调和轴性肌阵挛。32岁时他被转诊至我们的神经科门诊,表现为认知障碍、小脑综合征、轴性肌阵挛和表情减少,无其他帕金森病体征。由于无家族史,他按照脊髓性共济失调疾病的诊断流程进行了检查。后来,他出现了假性球麻痹、认知恶化、右上肢轻瘫和痉挛性截瘫。随后的检查发现了PSEN1 P117L突变,从而做出了常染色体显性AD的诊断。该病例说明了新发PSEN1突变的非典型表现所带来的诊断挑战,导致了不必要的检查。基因研究对于明确诊断可能至关重要。