Fujisawa Jumpei, Mutoh Tomokazu, Kawamura Kengo, Sawada Nami, Ono Daisuke, Yamaguchi Tetsuo, Morioka Ichiro
Department of Pediatrics and Child Health, Nihon University School of Medicine, Tokyo, Japan,
Department of Acute Medicine, Nihon University School of Medicine, Tokyo, Japan.
Infect Drug Resist. 2018 Oct 31;11:2063-2067. doi: 10.2147/IDR.S182659. eCollection 2018.
was the main causative organism for acute epiglottitis in the pre- type b (Hib) vaccine era. However, with current widespread Hib vaccination, the causative organisms may have changed. Here, we report the case of a healthy infant with acute epiglottitis caused by community-acquired methicillin-resistant (MRSA). The patient was a healthy 17-day-old male infant without a family history of immunodeficiency syndrome. He had not been started on any vaccines. On the third day of illness, he was diagnosed with acute pharyngitis with exudation on the back of the larynx. Although treatment using cefotaxime was initiated, he showed stridor, difficulty in pronunciation, and cyanosis upon crying on the fourth day. On the fifth day, he was diagnosed with acute epiglottitis by laryngoscopy, which showed a downward spread of the exudation and laryngeal edema. He was intubated and started on artificial respiration. Due to the detection of MRSA from a pharyngeal swab culture, he was treated with vancomycin. His fever disappeared on the first day after admission, and he was extubated on the eighth day after admission. MRSA genome analysis of the patient sample revealed negative Panton-Valentine leukocidin, positive toxic shock syndrome toxin 1, and type IV clone of staphylococcal cassette chromosome . This is a first case of acute epiglottitis caused by MRSA with a Panton-Valentine leukocidin-negative and toxic shock syndrome toxin 1-positive staphylococcal cassette chromosome type IV clone, which is known as a community-acquired MRSA in Japan. Community-acquired MRSA may be considered a causative organism for acute epiglottitis in the post-Hib vaccine era.
在b型流感嗜血杆菌(Hib)疫苗接种前的时代,[病原体名称未给出]是急性会厌炎的主要致病微生物。然而,随着目前Hib疫苗的广泛接种,致病微生物可能已经发生了变化。在此,我们报告一例由社区获得性耐甲氧西林金黄色葡萄球菌(MRSA)引起的急性会厌炎的健康婴儿病例。该患者是一名健康的17日龄男婴,无免疫缺陷综合征家族史。他尚未开始接种任何疫苗。在患病的第三天,他被诊断为急性咽炎,喉部后方有渗出物。尽管开始使用头孢噻肟进行治疗,但在第四天他出现了喘鸣、发音困难和哭闹时发绀的症状。在第五天,通过喉镜检查诊断为急性会厌炎,显示渗出物向下蔓延和喉部水肿。他接受了插管并开始进行人工呼吸。由于从咽拭子培养物中检测到MRSA,他接受了万古霉素治疗。他入院后第一天发热消失,入院后第八天拔管。对患者样本进行的MRSA基因组分析显示,Panton-Valentine杀白细胞素阴性、中毒性休克综合征毒素1阳性,以及葡萄球菌盒式染色体IV型克隆。这是首例由MRSA引起的急性会厌炎病例,该MRSA具有Panton-Valentine杀白细胞素阴性和中毒性休克综合征毒素1阳性的葡萄球菌盒式染色体IV型克隆,在日本被称为社区获得性MRSA。在Hib疫苗接种后的时代,社区获得性MRSA可能被认为是急性会厌炎的致病微生物。