Clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) in a child with ataxia and diplopia

E. Os, Malou Nijhuis, S. Malm
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Abstract

We report the case of a 15-year-old boy with clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). He presented with diplopia and ataxia and his cerebrospinal fluid showed mild pleocytosis and elevated protein. MRI demonstrated a reversible splenial lesion in the corpus callosum. He did not receive any treatment and recovered quickly within two weeks. Results of neurological examination after 3 months were completely normal. MERS is relatively unknown in Europe. The majority of patients are reported in East Asia. This post-infectious encephalitis/encephalopathy arises soon after the onset of symptoms. The prognosis is excellent and most patients recover completely without neurological sequelae. MRI typically shows a reversible splenial lesion with diffusion restriction and without contrast enhancement, sometimes with adjacent symmetrical lesions extending into the subcortical white matter. The pathogenesis is still unknown. Recognition of the condition and its clinic-radiological discrimination from acute disseminated encephalomyelitis may prevent unnecessary treatment.
共济失调和复视儿童的临床轻度脑炎/脑病伴可逆性脾损害(MERS)
我们报告一例15岁的男孩临床轻度脑炎/脑病伴可逆性脾损害(MERS)。他表现为复视和共济失调,脑脊液显示轻度细胞增多和蛋白升高。MRI显示胼胝体有可逆性脾损伤。他没有接受任何治疗,并在两周内迅速康复。3个月后神经系统检查结果完全正常。中东呼吸综合征在欧洲相对不为人知。据报道,大多数患者发生在东亚。这种感染后脑炎/脑病在出现症状后不久出现。预后良好,大多数患者完全康复,无神经系统后遗症。MRI典型表现为可逆性脾病变,扩散受限,无增强,有时伴有邻近对称病变,延伸至皮层下白质。发病机制尚不清楚。对急性播散性脑脊髓炎的认识及其临床影像学鉴别可以避免不必要的治疗。
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