Renthal William, Marin-Valencia Isaac, Evans Patricia A
Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas; Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas.
Pediatr Neurol. 2014 Jul;51(1):100-3. doi: 10.1016/j.pediatrneurol.2014.03.025. Epub 2014 Mar 30.
We present a developmentally appropriate adolescent boy who presented with upper and lower extremity glove-and-stocking paresthesias, distal weakness, vertigo, high-pitched voice, inattention, ataxia, and binocular diplopia after a voluntary 59-kg weight loss over 5 months.
Extensive investigations revealed serum thiamine levels <2 nmol/L. Brain magnetic resonance imaging revealed symmetric abnormal T2 prolongation of the mammillary bodies. Nerve conduction studies were consistent with axonal, length-dependent polyneuropathy. Together, these findings were diagnostic for peripheral polyneuropathy and Wernicke encephalopathy secondary to thiamine deficiency.
This patient illustrates that eating disorders can be an uncommon cause of rapidly progressive paresthesias, weakness, and neurological decline due to thiamine deficiency.
我们介绍一名发育正常的青少年男性,他在5个月内自愿减重59公斤后,出现了上下肢手套-袜套样感觉异常、远端无力、眩晕、高音调嗓音、注意力不集中、共济失调和双眼复视。
广泛检查发现血清硫胺素水平<2 nmol/L。脑部磁共振成像显示乳头体对称的T2信号延长异常。神经传导研究结果与轴索性、长度依赖性多发性神经病一致。综合这些发现,诊断为硫胺素缺乏继发的周围性多发性神经病和韦尼克脑病。
该患者表明,饮食失调可能是硫胺素缺乏导致快速进展的感觉异常、无力和神经功能衰退的罕见原因。