Department of Pediatrics, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The Netherlands.
Eur J Clin Microbiol Infect Dis. 2010 Nov;29(11):1315-9. doi: 10.1007/s10096-010-0999-7. Epub 2010 Jun 17.
We describe a 15-year-old patient with X-linked agammaglobulinemia who developed malabsorption and bacteremia due to infection of Helicobacter pylori and Campylobacter jejuni. The Campylobacter bacteremia was only recognized after subculturing of blood culture bottles that failed to signal in the automated system. After 2 weeks of treatment with meropenem and erythromycin for 4 weeks, the patient developed a relapse of bacteremia 10 months later with a high level erythromycin resistant C. jejuni. Sequencing revealed an A2058C mutation in the 23 S rRNA gene associated with this resistance. Treatment with doxycycline for 4 weeks finally resulted in complete eradication. This case report illustrates the importance for physicians to use adapted culture methods and adequate prolonged therapy in patients with an immunodeficiency. A summary of published case reports and series of patients with hypogammaglobulinemia or agammaglobulinemia with Campylobacter or Helicobacter bacteremia is given.
我们描述了一例 15 岁的 X 连锁无丙种球蛋白血症患者,由于感染幽门螺杆菌和空肠弯曲菌而导致吸收不良和菌血症。空肠弯曲菌菌血症仅在血培养瓶的亚培养后才被识别,这些血培养瓶在自动系统中未能发出信号。在使用美罗培南和红霉素治疗 2 周 4 周后,患者在 10 个月后出现菌血症复发,且高水平的红霉素耐药空肠弯曲菌。测序显示与这种耐药性相关的 23 S rRNA 基因中的 A2058C 突变。用多西环素治疗 4 周最终完全清除。本病例报告说明了在免疫缺陷患者中,医生使用适应性培养方法和足够的延长治疗的重要性。本文还总结了发表的病例报告和伴有低丙种球蛋白血症或无丙种球蛋白血症的患者系列,这些患者有空肠弯曲菌或幽门螺杆菌菌血症。