Global Pediatric Health (Jan 2019)

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

  • Kaori Kamijo MD,
  • Yoshifusa Abe MD, PhD,
  • Takehi Kagami MD,
  • Kazuhisa Ugajin ICMT,
  • Takeshi Mikawa MD,
  • Kunihiko Fukuchi MD, PhD,
  • Masaru Tatsuno MD, PhD,
  • Kazuo Itabashi MD, PhD

DOI
https://doi.org/10.1177/2333794X18821944
Journal volume & issue
Vol. 6

Abstract

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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 10 5 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.