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入院时仅以发热和颈淋巴结肿大为表现的严重川崎病。

A severe form of Kawasaki disease presenting with only fever and cervical lymphadenopathy at admission.

机构信息

Division of Pediatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Sakuragaoka, Kagoshima, Japan.

出版信息

J Pediatr. 2010 May;156(5):786-91. doi: 10.1016/j.jpeds.2009.11.042. Epub 2010 Jan 25.

DOI:10.1016/j.jpeds.2009.11.042
PMID:20097355
Abstract

OBJECTIVE

To examine the characteristics of patients with Kawasaki disease (KD) presenting with only fever and cervical lymphadenopathy at admission.

STUDY DESIGN

The laboratory and clinical findings of patients with definite KD presenting with only fever and cervical lymphadenopathy at admission (KDiL) were compared with those of all other patients with KD.

RESULTS

Sixteen patients with KDiL (8.6%) and 171 patients without KDiL were examined. The patients with KDiL were significantly older (KDiL/non-KDiL: 4.9+/-2.5/2.2+/-1.9 years) and admitted earlier (3.0+/-1.2/3.9+/-1.3 days of illness) than the patients without KDiL. They also showed significantly elevated white blood cell counts and C-reactive protein levels. Patients with KDiL were treated with the same dose of intravenous immunoglobulin as the patients without KDiL but were treated slightly later and had significantly higher frequency of additional intravenous immunoglobulin treatment (38%/10%) and coronary artery abnormalities (25%/5%). After adjustment for age, white blood cell count, and day of illness at admission or first intravenous immunoglobulin administration, the presence of KDiL significantly increased the risk of being a nonresponder to IVIG treatment or development of a coronary artery abnormality.

CONCLUSIONS

KDiL indicates a severe form of KD associated with increased risks of additional intravenous immunoglobulin treatment and coronary artery abnormalities. Patients with KDiL may require heightened surveillance and more aggressive treatment.

摘要

目的

探讨仅以发热和颈部淋巴结肿大起病的川崎病(KD)患者的临床特征。

研究设计

将入院时仅以发热和颈部淋巴结肿大起病的川崎病患者(KDiL)的实验室和临床检查结果与所有其他川崎病患者进行比较。

结果

共检查了 16 例 KDiL 患者(8.6%)和 171 例非 KDiL 患者。KDiL 患者明显年龄较大(KDiL/非 KDiL:4.9±2.5/2.2±1.9 岁)且入院时间更早(KDiL/非 KDiL:3.0±1.2/3.9±1.3 天)。他们的白细胞计数和 C 反应蛋白水平也明显升高。KDiL 患者与非 KDiL 患者接受相同剂量的静脉注射免疫球蛋白治疗,但治疗时间略晚,需要额外静脉注射免疫球蛋白治疗的频率明显更高(38%/10%),且冠状动脉异常的发生率更高(25%/5%)。在校正年龄、白细胞计数和入院或首次静脉注射免疫球蛋白治疗的天数后,KDiL 的存在显著增加了对 IVIG 治疗无反应或发生冠状动脉异常的风险。

结论

KDiL 表明川崎病的一种严重形式,与需要额外静脉注射免疫球蛋白治疗和冠状动脉异常的风险增加有关。KDiL 患者可能需要加强监测和更积极的治疗。

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