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[与肺炎支原体感染相关的急性脑干和纹状体脑病病例]

[Case of acute brainstem and striatal encephalopathy associated with Mycoplasma pneumoniae infection].

作者信息

Okumura Keiko, Aizaki Kouichi, Tsuru Tomohiko

机构信息

Department of Pediatrics, Matsudo City Hospital, Matsudo, Chiba.

出版信息

No To Hattatsu. 2011 Nov;43(6):471-5.

Abstract

Acute encephalopathy with bilateral striatal necrosis (EBSN) is a rare reversible neurological disease characterized by an abrupt onset following an acute infectious disease and by severe extra-pyramidal signs associated with striatal lesions. Brainstem involvement is rarely observed in this disease. We report a 10-year-old boy who had EBSN associated with Mycoplasma pneumoniae. He became lethargic after acute bronchitis. A few days later, he showed extra-pyramidal signs, pyramidal signs and overactive urinary bladder symptoms. Cranial T2-weighted and diffusion-weighted magnetic resonance imaging (MRI) demonstrated high-signal intensity in the bilateral striatum and substantia nigra. These symptoms improved soon after the administration of L-dopa in the acute phase. The effects of corticosteroids were not apparent in the acute phase. The serum particle agglutination titers against Mycoplasma pneumoniae determined on admission, the 12th hospital day and 2 months later were 1:2,560, 1:2,560 and 1:320, respectively. Two years later, a mild tic was observed. A mild atrophy was noted in the bilateral basal ganglia, but not in the substantia nigra on cranial MRI. This case is the first reported one with EBSN with the presence of an overactive urinary bladder, which could possibly caused by loss of dopaminergic inhibition.

摘要

急性脑病伴双侧纹状体坏死(EBSN)是一种罕见的可逆性神经系统疾病,其特征为急性感染性疾病后突然起病,并伴有与纹状体病变相关的严重锥体外系体征。该疾病很少观察到脑干受累情况。我们报告一名10岁男孩,患有与肺炎支原体相关的EBSN。他在急性支气管炎后变得嗜睡。几天后,出现锥体外系体征、锥体束征和膀胱过度活动症状。头颅T2加权和扩散加权磁共振成像(MRI)显示双侧纹状体和黑质高信号强度。急性期给予左旋多巴后这些症状很快改善。急性期皮质类固醇的效果不明显。入院时、住院第12天和2个月后测定的抗肺炎支原体血清颗粒凝集效价分别为1:2560、1:2560和1:320。两年后,观察到轻度抽搐。头颅MRI显示双侧基底节轻度萎缩,但黑质未见萎缩。该病例是首例报告的伴有膀胱过度活动的EBSN,这可能是由于多巴胺能抑制丧失所致。

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