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Infection-Associated Opsoclonus: A Retrospective Case Record Analysis and Review of Literature

机译:感染相关的Opsoclonus:一种回顾性案例记录分析和文学综述

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Opsoclonus, an uncommon clinical sign, and is often described in the context of opsoclonus myoclonus ataxia syndrome (OMAS). OMAS may be paraneoplastic or postinfectious. However, opsoclonus with or without OMAS may occur in association with a wide gamut of infections. Infection-associated opsoclonus/OMAS (IAO) needs recognition as a separate entity, since it demands relatively brief immunosuppression, symptomatic treatment, and has a better outcome. Case records of children, who presented with opsoclonus to a tertiary-care teaching hospital of North India over a period of 1 year (2017-2018), were reviewed. Those with opsoclonus in the setting of an acute infection/febrile illness (symptomatic opsoclonus; IAO) were included. Of 15 children with opsoclonus, 6 children [median age: 42 months (range: 8 months to 7 years); 2 boys] had opsoclonus associated with an infective or febrile illness. Additional clinical findings in these children included myoclonus (n = 2), ataxia (n = 4) and behavioral abnormalities (n = 4). All these patients had an associated neurologic or nonneurologic illness- scrub typhus (n = 1), tuberculous meningitis (n = 1), mumps encephalitis (n = 1), brainstem encephalitis (n = 1), acute cerebellitis (n = 1), and subacute sclerosing panencephalitis (SSPE, n = 1). Children with acute cerebellitis, brainstem encephalitis, and mumps encephalitis were treated with steroids while those with scrub typhus, tuberculosis, and SSPE were treated with antibiotics, antitubercular therapy, and Isoprinosine, respectively. None of them needed long-term maintenance immunotherapy. The evaluation for tumor was negative in all. Three of the 6 children are functionally normal at the last follow-up. Acute neuro infections may trigger opsoclonus. A careful analysis of clinical data and suitable investigations can help differentiate these children from those with OMAS. This distinction may avoid unwarranted long-term immunosuppression.
机译:Opsoclonus,一种罕见的临床符号,通常在Opsoclonus肌糖苷共济病综合征(OMAS)的背景下描述。 OMAS可能是副植物蛋白或后育。然而,具有或没有OMAS的Ophsoclonus可能与广泛的感染结合发生。感染相关的Opsoclonus / OMAS(IAO)需要识别作为单独的实体,因为它需要相对短暂的免疫抑制,对症治疗,并且具有更好的结果。审查了在1年(2017-2018)中向北印度北印度院校教学医院提供的儿童案例记录。在急性感染/发热疾病(症状Ophsoclonus; IAO)的设置中,有关Ophsoclonus的那些。 15名患有Opsoclonus,6名儿童[中位年龄:42个月(范围:8个月至7年); 2个男孩]有与感染或发热疾病相关的蛋白酶。这些儿童的其他临床发现包括肌阵挛(n = 2),共济失调(n = 4)和行为异常(n = 4)。所有这些患者有一个相关的神经系统或非血液疾病 - 磨砂动鼠(n = 1),结核性脑膜炎(n = 1),腮腺炎脑炎(n = 1),脑干脑炎(n = 1),急性细胞炎(n = 1) ,和亚急性硬化的终连脑炎(SSPE,N = 1)。患有急性脑炎,脑干脑炎和腮腺炎的儿童用类固醇治疗,同时用抗生素,抗细胞疗法和异丙胺治疗那些用磨砂动脉毛刺,结核病和SSPE进行治疗。它们都不需要长期维护免疫疗法。肿瘤的评价在所有情况下都是阴性的。在最后一次随访中,6名儿童中的三个儿童在功能正常。急性神经感染可能会引发Opsoclonus。仔细分析临床资料和合适的调查可以帮助将这些儿童与OMAS的那些区分开来。这种区别可能避免了无根据的长期免疫抑制。

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