Mycoplasma pneumoniae associated opsoclonus-myoclonus syndrome in three cases

被引:31
作者
Huber, Benedikt Maria [2 ]
Strozzi, Susi [3 ]
Steinlin, Maja [3 ]
Aebi, Christoph [4 ]
Fluri, Simon [1 ]
机构
[1] Inselspital Bern, Univ Hosp, Dept Pediat, Multidisciplinary Neonatal & Pediat Intens Care U, CH-3010 Bern, Switzerland
[2] Div Gen Pediat, Bern, Switzerland
[3] Div Pediat Neurol, Bern, Switzerland
[4] Inst Infect Dis, Bern, Switzerland
关键词
Opsoclonus-myoclonus-ataxia syndrome; M; pneumoniae; Neurologic disorder; Parainfectious; Paraneoplastic; Immunological mimicry; Children; Adolescents; NERVOUS-SYSTEM COMPLICATIONS; CHILDREN; INFECTION; AUTOANTIBODIES; NEUROBLASTOMA; LYMPHOCYTES; CHILDHOOD; DIAGNOSIS;
D O I
10.1007/s00431-009-1048-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:441 / 445
页数:5
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