Boulan-Predseil P, Vital A, Brochet B, Darriet D, Henry P, Vital C
Department of Neurology and Neuropathology, University of Bordeaux II, Pellegrin Hospital, France.
J Neurol. 1995 Aug;242(8):512-6. doi: 10.1007/BF00867422.
We describe a patient with adult polyglucosan body disease (APBD) who presented with a dementia of frontal lobe type (FLD), with a neurogenic bladder but no symptoms of sensory motor peripheral neuropathy. Diagnosis was made from a cerebral biopsy specimen which showed an accumulation of intra-axonal polyglucosan bodies in the central nervous system. This case differs from the usual presentation, in which gait disturbance is the main symptom and diagnosis is possible by sural nerve biopsy. Little is known about the neuropsychological pattern of APBD dementia but FLD has not previously been described. APBD is a heterogeneous clinical entity of unknown cause. This diagnosis must be considered in elderly patients with dementia.
我们描述了一名患有成人多聚糖体病(APBD)的患者,该患者表现为额叶型痴呆(FLD),伴有神经源性膀胱,但无感觉运动性周围神经病变症状。诊断依据是脑活检标本,该标本显示中枢神经系统中轴突内多聚糖体积聚。该病例与通常的表现不同,通常表现中步态障碍是主要症状,可通过腓肠神经活检进行诊断。关于APBD痴呆的神经心理学模式知之甚少,但此前尚未描述过FLD。APBD是一种病因不明的异质性临床实体。老年痴呆患者必须考虑这一诊断。