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川崎病咽后蜂窝织炎的危险因素。

Risk factors for retropharyngeal cellulitis in Kawasaki disease.

作者信息

Tona Risa, Shinohara Shogo, Fujiwara Keizo, Kikuchi Masahiro, Kanazawa Yuji, Kishimoto Ippei, Harada Hiroyuki, Naito Yasushi

机构信息

Department of Otolaryngology, Kobe City Medical Center General Hospital, Japan; Department of Otolaryngology, Institute of Biomedical Research and Innovation, Japan.

Department of Otolaryngology, Kobe City Medical Center General Hospital, Japan.

出版信息

Auris Nasus Larynx. 2014 Oct;41(5):455-8. doi: 10.1016/j.anl.2014.05.017. Epub 2014 Jun 20.

DOI:10.1016/j.anl.2014.05.017
PMID:24958366
Abstract

OBJECTIVE

Kawasaki disease (KD) is an acute multisystemic vasculitis of unknown etiology that occurs in infants and children. Retropharyngeal cellulitis has been reported as a rare manifestation of KD. This study investigated the frequency and characteristics of patients with KD manifesting as retropharyngeal soft-tissue swelling.

METHODS

We retrospectively reviewed 277 patients, with a mean age of 1 year and an age range of 7 months to 12 years, in whom KD had been diagnosed between 2005 and 2011.

RESULTS

In 10 patients (3.6%), contrast-enhanced computed tomography (CECT) showed low-density lesions without ring enhancement in the retropharyngeal spaces. These patients presented initially with fever and cervical lymphadenopathy, and were initially treated by their pediatricians for suppurative lymphadenitis (seven patients) or retropharyngeal abscess (three patients). KD was finally diagnosed either after antibiotics had been ineffective or when other symptoms characteristic of KD emerged.

CONCLUSION

Low-density lesions in the retropharyngeal space were identified by CECT in 3.6% of the KD patients. Early diagnosis of KD is essential because coronary artery lesions develop in 50% of untreated patients. If a child presents with fever, cervical lymphadenopathy, and swelling of the retropharyngeal space, KD should be included in the differential diagnoses.

摘要

目的

川崎病(KD)是一种病因不明的急性多系统血管炎,发生于婴幼儿和儿童。咽后蜂窝织炎已被报道为KD的一种罕见表现。本研究调查了表现为咽后软组织肿胀的KD患者的发生率和特征。

方法

我们回顾性分析了2005年至2011年间诊断为KD的277例患者,平均年龄1岁,年龄范围为7个月至12岁。

结果

10例患者(3.6%)的增强计算机断层扫描(CECT)显示咽后间隙有低密度病变,无环形强化。这些患者最初表现为发热和颈部淋巴结肿大,最初由儿科医生作为化脓性淋巴结炎(7例)或咽后脓肿(3例)进行治疗。在抗生素治疗无效或出现KD的其他特征性症状后最终确诊为KD。

结论

CECT在3.6%的KD患者中发现咽后间隙有低密度病变。KD的早期诊断至关重要,因为50%未经治疗的患者会发生冠状动脉病变。如果儿童出现发热、颈部淋巴结肿大和咽后间隙肿胀,鉴别诊断中应包括KD。

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