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Bacteriuria With CTX-M-8 Extended-Spectrum β-Lactamase–Producing Escherichia coli in a Patient With Incomplete Kawasaki Disease

机译:CTX-M-8广谱β-内酰胺酶引起的细菌尿症伴不完全川崎病患者

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摘要

We report the case of a 2-month-old infant with incomplete Kawasaki disease that presented as an apparent urinary tract infection. The patient’s fever persisted despite antibiotic treatment. Intravenous immunoglobulin and aspirin therapy cured both the incomplete Kawasaki disease and bacterial pyuria. Renal sonography, voiding cystourethrography, and renal parenchyma radionuclide scanning did not detect any abnormalities. Temporary dilation of the coronary artery was noted. In a urine specimen obtained through transurethral catheterization, the growth of 105 colony-forming units/mL of extended-spectrum β-lactamase–producing Escherichia coli was detected. Polymerase chain reaction analysis revealed that the enzyme genotype was CTX-M-8, which is a rare type in Japan. In conclusion, attention should be paid to a misleading initial presentation of fever and pyuria, which might be interpreted as urinary tract infection in patients with Kawasaki disease. Furthermore, pediatricians should consider incomplete Kawasaki disease when patients present with fever and pyuria, which are consistent with urinary tract infection, but do not respond to antibiotic treatment.
机译:我们报告了一个2个月大的不完全川崎病的婴儿病例,表现为明显的尿路感染。尽管进行了抗生素治疗,患者的发烧仍然持续。静脉注射免疫球蛋白和阿司匹林治疗可治愈不完全的川崎病和细菌性脓尿。肾脏超声检查,排尿膀胱尿道造影和肾实质放射性核素扫描均未发现任何异常。注意到冠状动脉暂时扩张。在通过经尿道导管插入术获得的尿液样本中,检测到10 5 集落形成单位/ mL产生广谱β-内酰胺酶的大肠杆菌的生长。聚合酶链反应分析显示该酶的基因型为CTX-M-8,在日本是罕见的类型。总之,应注意引起发热和脓尿的误导性最初表现,这可能被解释为川崎病患者的尿路感染。此外,当患者出现发烧和脓尿,这与尿路感染一致,但对抗生素治疗无反应时,儿科医生应考虑不完全的川崎病。

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