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川崎病肺部表现-诊断难题。

Pulmonary presentation of Kawasaki disease-A diagnostic challenge.

机构信息

Allergy Immunology Unit, Advanced Pediatrics Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Pulmonology Unit, Advanced Pediatrics Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Pediatr Pulmonol. 2018 Jan;53(1):103-107. doi: 10.1002/ppul.23885. Epub 2017 Sep 26.

Abstract

OBJECTIVES

Kawasaki disease (KD) is a multisystemic vasculitis with predominant mucocutaneous manifestations. Pulmonary involvement in KD is distinctly uncommon and is not commonly recognized. We describe our experience of managing children with KD wherein the initial presentation was predominantly pulmonary.

METHODS

Six hundred and two children have been diagnosed with KD during the period January 1993 to May 2017 in the Allergy Immunology Unit, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research, Chandigarh. Data were collected from inpatient records in Allergy Immunology Unit and follow-up files in the Pediatric Rheumatology Clinic.

RESULTS

Of 602 children, 11 (1.83%) had a predominant pulmonary presentation of KD. Mean age at diagnosis of KD was 2.5 years. Fever, cough and respiratory distress were the presenting complaints in all patients. First sign of KD was noted at a mean duration of 14.5 days from the onset of symptoms. Periungual desquamation was the most common clinical sign (72.7%). Persistent fever in spite of antimicrobials, thrombocytosis, and elevated erythrocyte sedimentation rate and C-reactive protein levels pointed toward a diagnosis of KD in our patients. Parenchymal consolidation was evident on chest X-ray in all patients, pleural effusion in six, empyema in three, and pneumothorax in two patients. Coronary artery abnormalities were evident in three patients. Intravenous immunoglobulin was given after a mean period of 22.4 days of onset of fever.

CONCLUSIONS

The diagnosis of KD is often delayed in children who have a predominantly pulmonary presentation. This can have adverse clinical consequences.

摘要

目的

川崎病(KD)是一种多系统血管炎,以黏膜皮肤表现为主。KD 肺部受累明显罕见,且不常见。我们描述了管理以肺部表现为主的 KD 患儿的经验。

方法

1993 年 1 月至 2017 年 5 月期间,在昌迪加尔 PGIMER 高级儿科中心过敏免疫科共诊断了 602 例 KD 患儿。数据来自过敏免疫科的住院病历和儿科风湿病诊所的随访档案。

结果

602 例患儿中,11 例(1.83%)KD 以肺部表现为主。KD 的平均诊断年龄为 2.5 岁。所有患者的首发症状均为发热、咳嗽和呼吸急促。KD 的首发症状平均在症状出现后 14.5 天出现。所有患者均出现甲周脱皮(72.7%),这是最常见的临床体征。尽管使用了抗生素,但仍持续发热、血小板增多、红细胞沉降率和 C 反应蛋白水平升高,这些都指向我们的患者 KD 诊断。所有患者的胸部 X 线片均可见肺实质实变,6 例有胸腔积液,3 例有脓胸,2 例有气胸。3 例患者存在冠状动脉异常。静脉注射免疫球蛋白在发热开始后平均 22.4 天使用。

结论

以肺部表现为主的患儿 KD 诊断往往被延误,这可能会产生不良的临床后果。

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