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青少年及儿童霍奇金淋巴瘤患者的临床表现:一项回顾性病例系列研究

Clinical Manifestation of Juvenile and Pediatric HD Patients: A Retrospective Case Series.

作者信息

Achenbach Jannis, Thiels Charlotte, Lücke Thomas, Saft Carsten

机构信息

Department of Neurology, Huntington Centre North Rhine-Westphalia, St. Josef-Hospital Bochum, Ruhr-University Bochum, 44791 Bochum, Germany.

Department of Neuropaediatrics and Social Paediatrics, University Children's Hospital, Ruhr-University Bochum, 44791 Bochum, Germany.

出版信息

Brain Sci. 2020 Jun 3;10(6):340. doi: 10.3390/brainsci10060340.

Abstract

BACKGROUND

Studies on the clinical manifestation and course of disease in children suffering from Huntington's disease (HD) are rare. Case reports of juvenile HD (onset ≤ 20 years) describe heterogeneous motoric and non-motoric symptoms, often accompanied with a delay in diagnosis. We aimed to describe this rare group of patients, especially with regard to socio-medical aspects and individual or common treatment strategies. In addition, we differentiated between juvenile and the recently defined pediatric HD population (onset < 18 years).

METHODS

Out of 2593 individual HD patients treated within the last 25 years in the Huntington Centre, North Rhine-Westphalia (NRW), 32 subjects were analyzed with an early onset younger than 21 years (1.23%, juvenile) and 18 of them younger than 18 years of age (0.69%, pediatric).

RESULTS

Beside a high degree of school problems, irritability or aggressive behavior (62.5% of pediatric and 31.2% of juvenile cases), serious problems concerning the social and family background were reported in 25% of the pediatric cohort. This includes an attempted rape and robbery at the age of 12, as problems caused by the affected children, but also alcohol-dependency in a two-year-old induced by a non-HD affected stepfather. A high degree of suicidal attempts and ideations (31.2% in pediatric and 33.3% in juvenile group) was reported, including drinking of solvents, swallowing razor blades or jumping from the fifth floor with following incomplete paraparesis. Beside dopaminergic drugs for treatment of bradykinesia, benzodiazepines and tetrabenazine for treatment of dystonia, cannabinoids, botulinum toxin injection and deep brain stimulation were used for the improvement of movement disorders, clozapine for the treatment of tremor, and dopa-induced hallucinations and zuclopenthixole for the treatment of severe aggressive behavior.

CONCLUSIONS

Beside abnormalities in behavior from an early age due to HD pathology, children seem to have higher socio-medical problems related to additional burden caused by early affected parents, instable family backgrounds including drug abuse of a parent or multiple changes of partners. Treatment required individualized strategies in many cases.

摘要

背景

关于亨廷顿舞蹈症(HD)患儿的临床表现及病程的研究较为罕见。青少年型HD(发病年龄≤20岁)的病例报告描述了多样的运动和非运动症状,诊断往往延迟。我们旨在描述这一罕见的患者群体,特别是在社会医学方面以及个体或通用治疗策略方面。此外,我们区分了青少年型HD和最近定义的儿童HD群体(发病年龄<18岁)。

方法

在过去25年里于北莱茵 - 威斯特法伦州(NRW)亨廷顿中心接受治疗的2593例HD患者中,分析了32例发病年龄小于21岁的早发型患者(1.23%,青少年型),其中18例年龄小于18岁(0.69%,儿童型)。

结果

除了严重的学业问题、易怒或攻击性行为(儿童型病例的62.5%,青少年型病例的31.2%)外,25%的儿童型队列报告了严重的社会和家庭背景问题。这包括一名12岁儿童企图强奸和抢劫,这是患病儿童引发的问题,还包括一名两岁儿童因非HD患者继父导致的酒精依赖。报告了高度的自杀企图和念头(儿童型组为31.2%,青少年型组为33.3%),包括饮用溶剂、吞服剃须刀片或从五楼跳下导致不完全性截瘫。除了使用多巴胺能药物治疗运动迟缓、苯二氮䓬类药物和丁苯那嗪治疗肌张力障碍外,还使用大麻素、肉毒杆菌毒素注射和深部脑刺激来改善运动障碍,使用氯氮平治疗震颤、多巴诱导的幻觉,以及使用珠氯噻醇治疗严重攻击性行为。

结论

除了因HD病理导致的早期行为异常外,儿童似乎还存在更高的社会医学问题,这些问题与患病早的父母带来的额外负担、包括父母药物滥用或伴侣多次更换在内的不稳定家庭背景有关。在许多情况下,治疗需要个体化策略。

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