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Diversity and combinations of infectious agents in 38 adults with an infection-triggered reactive haemophagocytic syndrome: a multicenter study

机译:多中心研究:38位感染触发的反应性噬血细胞综合征成人的感染因素的多样性和组合:

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Reactive haemophagocytic syndrome (HS) is a rare condition that occurs in patients with infections, haematological malignancies or autoimmune diseases. Although various microorganisms are thought to trigger HS, most of the literature data on this topic have been gathered in single-centre case series. Here, we sought to characterize infectious triggers in a large, multicentre cohort of patients with HS. Patients were included in the present study if HS was solely due to one or more infections. Detailed microbiological data were recorded. Of the 162 patients with HS in the cohort, 40 (25%) had at least one infection and 38 of the latter (including 14 women, 36.8%) were included. The median age was 46 years. Seven patients were presumed to be immunocompetent (18.4%), whereas 19 patients (50%) were infected with human immunodeficiency virus and 12 patients (31.6%) were immunocompromised for other reasons. Twenty-seven patients (71.1%) had a single infection, whereas six (15.8%) and five (13.1%) patients had, respectively, two and three concomitant infections. We observed pyogenic bacterial infections (n = 7), tuberculosis (n = 10), non-tuberculous mycobacteriosis (n = 3), viral infections (n = 17: 11 cytomegalovirus, three Epstein-Barr virus, two human herpesvirus 8, one herpes simplex virus 2), parasitic infections (n = 8: four disseminated toxoplasmosis, one leishmaniasis, three malaria), fungal infections (n = 5: four pulmonary pneumocystosis and one candidaemia). Eighteen patients (47.4%) received corticosteroids and/or etoposide. Twelve patients died (31.6%). All multiple infections and all deaths occurred in immunocompromised patients. When compared with patients suffering from malignancy-associated HS, patients with infection-triggered HS were younger and more likely to be immunocompromised, and had a better outcome. Clinical Microbiology and Infection (C) 2015 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
机译:反应性噬血细胞综合征(HS)是一种罕见的疾病,发生于感染,血液系统恶性肿瘤或自身免疫性疾病的患者中。尽管人们认为各种微生物会触发HS,但是有关该主题的大多数文献数据都是以单中心病例系列收集的。在这里,我们试图表征大量多中心HS患者的感染触发因素。如果HS仅由一种或多种感染引起,则将患者纳入本研究。记录详细的微生物学数据。在该队列的162例HS患者中,有40例(25%)至少感染了一种,其中38例(包括14名女性,占36.8%)。中位年龄为46岁。假定有7名患者具有免疫能力(18.4%),而19名患者(50%)被感染了人类免疫缺陷病毒,而12名患者(31.6%)因其他原因而免疫受损。二十七名患者(71.1%)患有单一感染,而六名(15.8%)和五名(13.1%)患者分别患有两例和三例并发感染。我们观察到化脓性细菌感染(n = 7),肺结核(n = 10),非结核分枝杆菌病(n = 3),病毒感染(n = 17:11巨细胞病毒,三种爱泼斯坦-巴尔病毒,两种人疱疹病毒8种,一种单纯疱疹病毒2),寄生虫感染(n = 8:4种弥散性弓形虫病,1种利什曼病,3种疟疾),真菌感染(n = 5:4种肺气肿和1例念珠菌血症)。 18名患者(47.4%)接受了皮质类固醇和/或依托泊苷。十二名患者死亡(31.6%)。所有多重感染和所有死亡均发生在免疫功能低下的患者中。与患有恶性肿瘤相关的HS的患者相比,感染触发的HS的患者更年轻,免疫功能更弱,预后更好。临床微生物学和感染(C)2015年欧洲临床微生物学和传染病学会。由Elsevier Ltd.出版。保留所有权利。

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