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[一例伴运动和感觉性多发性神经病的成人T细胞白血病/淋巴瘤]

[A case of adult T cell leukemia/lymphoma with motor and sensory polyneuropathy].

作者信息

Nakano S, Ohnishi A, Oishi T, Murai Y, Nagata K

机构信息

Department of Neurology, University of Occupational and Environmental Health.

出版信息

Rinsho Shinkeigaku. 1991 Aug;31(8):853-7.

PMID:1662570
Abstract

A 62-year-old man was admitted to our hospital because of two months continuing paresthesia and muscle weakness of distal portions of the four limbs. On general physical examination, skin lesions, lymphadenopathy and hepatosplenomegaly were not found. Neurological examination revealed moderate weakness in the bilateral distal muscles of the lower limbs and left distal muscles of the upper limbs, and slight weakness in the right distal muscles of the upper limbs and the bilateral proximal muscles of the four limbs. Hand grasping powers were 24 kg and 2 kg on the right and left, respectively. The biceps, triceps and radial reflexes were decreased on the right, but normal on the left. The Achilles tendon reflex was decreased on the right and absent on the left. Paresthesia and superficial sensory disturbance were observed with glove and stocking distribution, which was more severe on the left side. The vibration and position senses were slightly decreased in the distal part of the lower limbs. On the laboratory examinations, serum anti-HTLV-I antibody was positive and no abnormal lymphocytes were observed in peripheral blood. Cerebrospinal fluid findings were normal, and anti-HTLV-I antibody was negative. Motor and sensory conduction velocities were normal or slightly decreased in all of the limb nerves examined, but the amplitudes of the compound muscle action potentials and the sensory nerve action potentials were asymmetrically decreased. Needle EMG showed fibrillation potentials and giant spikes with a reduction in number of motor unit potentials. The histological examination of the biopsied sural nerve revealed severe axonal degeneration without evidence of vasculitis or infiltration of abnormal lymphocytes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一名62岁男性因四肢远端持续两个月的感觉异常和肌肉无力入院。全身体格检查未发现皮肤病变、淋巴结肿大和肝脾肿大。神经系统检查发现双下肢远端肌肉及左上肢远端肌肉中度无力,右上肢远端肌肉及四肢双侧近端肌肉轻度无力。右手握力和左手握力分别为24千克和2千克。右侧肱二头肌、肱三头肌和桡骨膜反射减弱,左侧正常。右侧跟腱反射减弱,左侧消失。感觉异常和浅感觉障碍呈手套和袜套样分布,左侧更严重。双下肢远端振动觉和位置觉轻度减退。实验室检查显示血清抗人嗜T淋巴细胞病毒I型(HTLV-I)抗体阳性,外周血未观察到异常淋巴细胞。脑脊液检查结果正常,抗HTLV-I抗体阴性。所有检查的肢体神经运动和感觉传导速度正常或轻度减慢,但复合肌肉动作电位和感觉神经动作电位的波幅不对称性降低。针极肌电图显示纤颤电位和巨大电位,运动单位电位数量减少。腓肠神经活检组织学检查显示严重轴索性变性,无血管炎或异常淋巴细胞浸润证据。(摘要截选至250字)

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J Neurovirol. 2005 Apr;11(2):199-207. doi: 10.1080/13550280590924197.