Mendoza-Palomar Natalia, Melendo-Pérez Susana, Balcells Joan, Izquierdo-Blasco Jaume, Martín-Gómez Maria Teresa, Velasco-Nuño Monica, Rivière Jacques G, Soler-Palacin Pere
Paediatric Infectious Diseases and Immunodeficiencies Unit, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Infection in the Immunosuppressed Paediatric Patient Research Group, Vall d'Hebron Research Institute, 08035 Barcelona, Spain.
J Fungi (Basel). 2021 Sep 5;7(9):726. doi: 10.3390/jof7090726.
A previously healthy 9-year-old girl developed fulminant myocarditis due to severe influenza A infection complicated with methicillin-resistant pneumonia, requiring extracorporeal membrane oxygenation (ECMO) support. Twelve days after admission, was isolated in tracheal aspirate, and 12 h later she suddenly developed anisocoria. Computed tomography (CT) of the head showed fungal brain lesions. Urgent decompressive craniectomy with lesion drainage was performed; histopathology found hyphae in surgical samples, culture-positive for (susceptible to azoles, echinocandins, and amphotericin B). Extension workup showed disseminated aspergillosis. After multiple surgeries and combined antifungal therapy (isavuconazole plus liposomal amphotericin B), her clinical course was favorable. Isavuconazole therapeutic drug monitoring was performed weekly. Extensive immunological study ruled out primary immunodeficiencies. Fluorine-18 fluorodeoxyglucose positron emission tomography/CT (F-FDG PET/CT) follow-up showed a gradual decrease in fungal lesions. Influenza-associated pulmonary aspergillosis is well-recognized in critically ill adult patients, but pediatric data are scant. Clinical features described in adults concur with those of our case. Isavuconazole, an off-label drug in children, was chosen because our patient had severe renal failure. To conclude, influenza-associated pulmonary aspergillosis is uncommon in children admitted to intensive care for severe influenza, but pediatricians should be highly aware of this condition to enable prompt diagnosis and treatment.
一名既往健康的9岁女孩因严重甲型流感感染并发耐甲氧西林肺炎,发展为暴发性心肌炎,需要体外膜肺氧合(ECMO)支持。入院12天后,在气管吸出物中分离出[具体病菌名称未给出],12小时后她突然出现瞳孔不等大。头部计算机断层扫描(CT)显示脑部有真菌病变。紧急进行了颅骨减压切除术并引流病变;组织病理学检查在手术样本中发现菌丝,培养结果为[具体病菌名称未给出]阳性(对唑类、棘白菌素类和两性霉素B敏感)。进一步检查显示为播散性曲霉病。经过多次手术和联合抗真菌治疗(艾沙康唑加脂质体两性霉素B),她的临床病程良好。每周进行艾沙康唑治疗药物监测。广泛的免疫学研究排除了原发性免疫缺陷。氟-18氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(F-FDG PET/CT)随访显示真菌病变逐渐减少。流感相关的肺曲霉病在重症成年患者中已得到充分认识,但儿科数据很少。成人中描述的临床特征与我们病例的特征一致。由于我们的患者患有严重肾衰竭,所以选择了儿童超说明书用药的艾沙康唑。总之,流感相关的肺曲霉病在因严重流感入住重症监护病房的儿童中并不常见,但儿科医生应高度警惕这种情况,以便能够及时诊断和治疗。