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首页> 外文期刊>BMC Infectious Diseases >Invasive mucormycosis in children: an epidemiologic study in European and non-European countries based on two registries
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Invasive mucormycosis in children: an epidemiologic study in European and non-European countries based on two registries

机译:儿童浸润性毛霉菌病:基于两个注册机构的欧洲和非欧洲国家的流行病学研究

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Background Mucormycosis has emerged as a rare but frequently fatal invasive fungal disease. Current knowledge on paediatric mucormycosis is based on case reports and small series reported over several decades. Contemporary data on a large cohort of patients is lacking. Methods Two large international registries (Zygomyco.net and FungiScope?) were searched for mucormycosis cases in ≤19 year-old patients. Cases enrolled between 2005 and 2014 were extracted, and dual entries in the two databases merged. Epidemiology, clinical characteristics, diagnostic procedures, therapeutic management and final outcome were recorded and analysed with SPSS v.12. Results Sixty-three unique cases (44 proven and 19 probable) were enrolled from 15 countries (54 in European and 9 in non-European countries). Median age was 13 years [Interquartile Range (IQR) 7.7] with a slight predominance (54.1 %) of females. Underlying conditions were haematological malignancies (46 %), other malignancies (6.3 %), haematopoietic stem cell transplantation (15.9 %), solid organ transplantation, trauma/surgery and diabetes mellitus (4.8 % each) and a variety of other diseases (7.9 %); in 9.5%, no underlying medical condition was found. Neutropenia was recorded in 46 % of the patients. The main sites of infection were lungs (19 %), skin and soft tissues (19 %), paranasal sinus/sino-orbital region (15.8 %) and rhino-cerebral region (7.9 %). Disseminated infection was present in 38.1 %. Mucormycosis diagnosis was based on several combinations of methods; culture combined with histology was performed in 31 cases (49.2 %). Fungal isolates included Rhizopus spp. (39.7 %), Lichtheimia spp . (17.5 %), Mucor spp. (12.7 %), Cunninghamella bertholletiae (6.3 %) and unspecified (23.8 %). Treatment comprised amphotericin B (AmB) monotherapy in 31.7 % or AmB in combination with other antifungals in 47.7 % of the cases, while 14.3 % received no antifungals. Surgery alone was performed in 6.3 %, and combined with antifungal therapy in 47.6 %. Crude mortality at last contact of follow-up was 33.3 %. In regression analysis, disseminated disease and prior haematopoietic stem cell transplantation were associated with increased odds of death, whereas the combination of systemic antifungal therapy with surgery was associated with improved survival. Conclusion Paediatric mucormycosis mainly affects children with malignancies, presents as pulmonary, soft tissue, paranasal sinus or disseminated disease and is highly lethal. Outcome is improved when active antifungal therapy and surgery are combined.
机译:背景技术毛霉菌病已作为一种罕见但经常致命的侵袭性真菌病出现。目前有关小儿毛霉菌病的知识是基于几十年来的病例报告和小系列报道。缺乏有关大量患者的当代数据。方法对两个大型国际注册机构(Zygomyco.net和FungiScope?)进行搜索,以寻找≤19岁患者的毛霉菌病病例。提取了2005年至2014年之间登记的病例,并合并了两个数据库中的双重条目。使用SPSS v.12记录并分析流行病学,临床特征,诊断程序,治疗管理和最终结果。结果来自15个国家(欧洲54例,非欧洲国家9例)的63例独特病例(44例确诊和19例可能)入选。中位年龄为13岁[四分位间距(IQR)7.7],女性为轻度优势(54.1%)。潜在的条件是血液系统恶性肿瘤(46%),其他恶性肿瘤(6.3%),造血干细胞移植(15.9%),实体器官移植,创伤/外科手术和糖尿病(各为4.8%)和其他多种疾病(7.9%) );在9.5%中,未发现潜在的医疗状况。在46%的患者中记录了中性粒细胞减少。感染的主要部位是肺(19%),皮肤和软组织(19%),鼻旁窦/窦眶区域(15.8%)和犀牛-大脑区域(7.9%)。传播感染的发生率为38.1%。毛霉菌病的诊断是基于几种方法的组合。 31例(49.2%)进行了组织学与组织学相结合的培养。真菌分离株包括根霉。 (39.7%),Lichtheimia spp。 (17.5%),Mucor spp。 (12.7%),Cunninghamella bertholletiae(6.3%)和未指定(23.8%)。治疗包括21.7%的两性霉素B(AmB)单药治疗或AmB联合其他抗真菌药的治疗占47.7%,而14.3%的患者未接受抗真菌药。单独手术占6.3%,与抗真菌治疗相结合占47.6%。最后一次随访的粗死亡率为33.3%。在回归分析中,播散性疾病和先前的造血干细胞移植与死亡几率增加相关,而全身性抗真菌治疗与手术相结合可提高生存率。结论小儿毛霉菌病主要影响儿童恶性肿瘤,表现为肺,软组织,鼻旁窦或弥漫性疾病,具有高致死性。积极的抗真菌治疗和手术相结合,结果得到改善。

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