Mizuno Y, Komori S, Shigetomo R, Kurihara E, Tamagawa K, Komiya K
Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, Japan.
Brain Dev. 1995 Mar-Apr;17(2):126-9. doi: 10.1016/0387-7604(94)00125-h.
A case of Hopkins syndrome is presented. The patient was a 4-year-old boy who developed weakness of the right leg 2-3 days after a mild asthmatic attack. Needle electromyography revealed fasciculation discharges in the right gastrocnemius muscle. A histological study of the biopsied right quadriceps femoris muscle revealed scattered atrophic fibers, indicating lesions in the anterior horn cells of the spinal cord. This is the first reported case of Hopkins syndrome including muscle pathology.
本文报告一例霍普金斯综合征病例。患者为一名4岁男孩,在轻度哮喘发作后2 - 3天出现右腿无力。针极肌电图显示右腓肠肌有肌束震颤放电。对活检的右股四头肌进行组织学研究,发现散在的萎缩纤维,提示脊髓前角细胞有病变。这是首例报道的包括肌肉病理学表现的霍普金斯综合征病例。