Department of Pediatrics, University Hospital, Inselspital, Bern, Switzerland.
Eur J Pediatr. 2010 Apr;169(4):441-5. doi: 10.1007/s00431-009-1048-3. Epub 2009 Sep 24.
Opsoclonus-myoclonus syndrome (OMS) is a rare acquired movement disorder occurring in all age groups, predominantly in infants. Although the exact pathogenesis is still undefined, there is strong evidence for a paraneoplastic or parainfectious immune process resulting in central nervous system dysfunction. Mycoplasma pneumoniae has been implicated in a number of immune-mediated neurologic diseases [28]. However, the association of M. pneumoniae and opsoclonus-myoclonus-ataxia syndrome is not well established so far. We present three cases with opsoclonus-myoclonus-ataxia syndrome in adolescents following an infection with M. pneumoniae. Monophasic disease course and full recovery correspond to the favorable prognosis known from parainfectious cases in young adults. This should affect therapeutic consideration. OMS should be added to the spectrum of M. pneumoniae-associated neurologic complications. Nevertheless, neuroblastoma has to be ruled out in all cases of OMS.
眼-口-肌阵挛-共济失调综合征(OMS)是一种罕见的获得性运动障碍,可发生于所有年龄段,主要见于婴儿。尽管确切的发病机制仍未明确,但有强有力的证据表明其与副肿瘤或感染后免疫过程导致中枢神经系统功能障碍有关。肺炎支原体已被牵涉到许多免疫介导的神经系统疾病[28]中。然而,肺炎支原体与眼-口-肌阵挛-共济失调综合征的关联尚未得到充分确立。我们报告了 3 例青少年在感染肺炎支原体后出现眼-口-肌阵挛-共济失调综合征。单相病程和完全恢复与年轻人感染后副肿瘤病例的良好预后一致。这应影响治疗考虑。眼-口-肌阵挛-共济失调综合征应添加到肺炎支原体相关神经系统并发症的范围内。然而,在所有眼-口-肌阵挛-共济失调综合征的病例中都必须排除神经母细胞瘤。