Kawasaki disease and sensorineural hearing loss: an (un)expected complication.

IF 2.6 3区 医学 Q1 PEDIATRICS European Journal of Pediatrics Pub Date : 2012-05-01 Epub Date: 2012-01-07 DOI:10.1007/s00431-011-1667-3
Ana Novo, Susana Pinto, Ana Catarina Prior, Sílvia Alvares, Teresa Soares, Margarida Guedes
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引用次数: 25

Abstract

Unlabelled: Kawasaki disease (KD) is an acute, self-limiting, idiopathic form of vasculitis. The preventive effect of early therapy on coronary artery aneurysms, the hallmark of the disease, is well established. The spectrum of complication includes not only cardiac involvement but also central nervous system lesions. We report a 4-year-old boy with a clinical presentation suggestive of KD treated with intravenous immunoglobulin and acetylsalicylic acid. Clinical manifestations regressed within 24 hours and cardiac anomalies were not seen. Two weeks later, the parents noticed a sudden absence of response to sound stimuli. Investigations confirmed bilateral severe sensorineural hearing loss for which oral steroid therapy was given. This resulted in an improvement only on the right side, with severe hearing loss persisting on the left.

Conclusion: Sensorineural hearing loss is an uncommonly reported complication of KD. Pediatricians should be aware of this potential complication to allow for early intervention.

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川崎病和感音神经性听力损失:一种(未预料到的)并发症。
未标示:川崎病(KD)是一种急性、自限性、特发性血管炎。冠状动脉动脉瘤是该病的标志,早期治疗的预防作用已得到证实。并发症不仅包括心脏受累,还包括中枢神经系统病变。我们报告一个4岁男孩的临床表现提示KD治疗与静脉注射免疫球蛋白和乙酰水杨酸。临床表现在24小时内消退,未见心脏异常。两周后,父母注意到孩子突然对声音刺激失去了反应。调查证实双侧严重感音神经性听力损失,给予口服类固醇治疗。结果只有右侧听力有所改善,左侧听力持续严重受损。结论:感觉神经性听力损失是KD的罕见并发症。儿科医生应该意识到这种潜在的并发症,以便进行早期干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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