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以淋巴结病和发热为唯一初始表现的川崎病。

Kawasaki disease with lymphadenopathy and fever as sole initial manifestations.

作者信息

Kubota Masaru, Usami Ikuya, Yamakawa Masaru, Tomita Yasuhiko, Haruta Tsunekazu

机构信息

Faculty of Human Life and Environment, Nara Women's University, Nara, Japan.

出版信息

J Paediatr Child Health. 2008 Jun;44(6):359-62. doi: 10.1111/j.1440-1754.2008.01310.x.

Abstract

AIM

Initial presentation with only cervical lymphadenopathy and fever is one of the pitfalls in the diagnosis of Kawasaki disease (KD). As the number of such patients is small, their clinical features have remained uncertain. The purpose of the present study is to characterise the features of such KD patients, especially in comparison with those of patients with common onset.

METHODS

We conducted a retrospective review of the medical records of 136 consecutive KD patients admitted to Kobe City General Hospital from April of 2000 to March of 2006. Twenty-nine of the 136 patients initially presented with only cervical lymphadenopathy and fever and were classified into the lymphadenopathy-KD (LKD); they were compared with the remaining 107 KD patients with other presentations (other-KD).

RESULTS

Age, days of fever to diagnosis, and duration of fever were significantly higher or longer in LKD patients, who also showed higher C-reactive protein levels and neutrophil alkaline phosphatase activity. There were no significant differences between two groups in gender, duration of hospitalization, frequency of high-dose intravenous immunoglobulin (IVIG) administration, coronary artery lesions (CALs), white blood cell or platelet counts, and levels of hemoglobin or albumin on admission.

CONCLUSIONS

Although a delay in diagnosis and stronger inflammation were found in LKD patients, such differences did not have any significant effect on patients' outcomes as assessed by the frequency of IVIG administration and the presence of CALs.

摘要

目的

初发时仅有颈部淋巴结病和发热是川崎病(KD)诊断中的陷阱之一。由于这类患者数量较少,其临床特征尚不确定。本研究的目的是描述这类KD患者的特征,尤其是与常见发病患者的特征进行比较。

方法

我们对2000年4月至2006年3月期间连续入住神户市立综合医院的136例KD患者的病历进行了回顾性研究。136例患者中有29例初发时仅有颈部淋巴结病和发热,被归类为淋巴结病型KD(LKD);将他们与其余107例有其他表现的KD患者(其他型KD)进行比较。

结果

LKD患者的年龄、诊断前发热天数和发热持续时间显著更高或更长,其C反应蛋白水平和中性粒细胞碱性磷酸酶活性也更高。两组在性别、住院时间、大剂量静脉注射免疫球蛋白(IVIG)给药频率、冠状动脉病变(CALs)、白细胞或血小板计数以及入院时血红蛋白或白蛋白水平方面无显著差异。

结论

虽然在LKD患者中发现了诊断延迟和更强的炎症反应,但这些差异对通过IVIG给药频率和CALs的存在评估的患者预后没有任何显著影响。

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