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以淋巴结首发的川崎病与无颈淋巴结病的川崎病的比较。

Comparison between Kawasaki disease with lymph-node-first presentation and Kawasaki disease without cervical lymphadenopathy.

作者信息

Kim Jung Ok, Kim Yeo Hyang, Hyun Myung Chul

机构信息

Department of Pediatrics, Jeju National University Hospital, Jeju, Korea.

Department of Pediatrics, Kyungpook National University School of Medicine, Daegu, Korea.

出版信息

Korean J Pediatr. 2016 Feb;59(2):54-8. doi: 10.3345/kjp.2016.59.2.54. Epub 2016 Feb 29.

Abstract

PURPOSE

We evaluated the characteristics of patients with Kawasaki disease (KD) who presented with only fever and cervical lymphadenopathy on admission, and compared them with the characteristics of those who presented with typical features but no cervical lymphadenopathy.

METHODS

We enrolled 98 patients diagnosed with KD. Thirteen patients had only fever and cervical lymphadenopathy on the day of admission (group 1), 31 had typical features with cervical lymphadenopathy (group 2), and 54 had typical features without cervical lymphadenopathy (group 3).

RESULTS

The mean age (4.3±2.1 years) and duration of fever (7.5±3.6 days) before the first intravenous immunoglobulin (IVIG) administration were highest in group 1 (P=0.001). Moreover, this group showed higher white blood cell and neutrophil counts, and lower lymphocyte counts after the first IVIG administration as compared to the other groups (P=0.001, P=0.001, and P=0.003, respectively). Group 1 also had a longer duration of hospitalization and higher frequency of second-line treatment as compared to groups 2 and 3 (group 1 vs. group 2, P=0.000 and P=0.024; group 1 vs. group 3, P=0.000 and P=0.007). A coronary artery z score of >2.5 was frequently observed in group 1 than in group 3 (P=0.008).

CONCLUSION

KD should be suspected in children who are unresponsive to antibiotics and have prolonged fever and cervical lymphadenopathy, which indicates that KD is associated with the likelihood of requiring second-line treatment and risk of developing coronary artery dilatation.

摘要

目的

我们评估了入院时仅表现为发热和颈部淋巴结肿大的川崎病(KD)患者的特征,并将其与表现为典型特征但无颈部淋巴结肿大的患者特征进行比较。

方法

我们纳入了98例诊断为KD的患者。13例患者在入院当天仅表现为发热和颈部淋巴结肿大(第1组),31例具有典型特征并伴有颈部淋巴结肿大(第2组),54例具有典型特征但无颈部淋巴结肿大(第3组)。

结果

第1组首次静脉注射免疫球蛋白(IVIG)前的平均年龄(4.3±2.1岁)和发热持续时间(7.5±3.6天)最高(P = 0.001)。此外,与其他组相比,该组首次IVIG注射后白细胞和中性粒细胞计数更高,淋巴细胞计数更低(分别为P = 0.001、P = 0.001和P = 0.003)。与第2组和第3组相比,第1组的住院时间更长,二线治疗频率更高(第l组与第2组,P = 0.000和P = 0.024;第1组与第3组,P = 0.000和P = 0.007)。第1组比第3组更常观察到冠状动脉z评分>2.5(P = 0.008)。

结论

对于对抗生素无反应、发热持续时间长且有颈部淋巴结肿大的儿童,应怀疑患有KD,这表明KD与需要二线治疗的可能性以及发生冠状动脉扩张的风险相关。

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