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Brucella bacteremia in a recipient of an allogeneic hematopoietic stem cell transplant: a case report

机译:异基因造血干细胞移植受者中的布鲁氏菌菌血症:一例报告

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Background Brucellosis is an important cause of morbidity and mortality in patients living in areas that are endemic for the infection. Case Presentation A 20 years old Saudi male was diagnosed to have severe aplastic anemia at King Faisal Specialist Hospital and Research Centre in Riyadh in April 2006. One hundred and twelve days following his successful allogeneic hematopoietic stem cell transplant, he presented with pyrexia in addition to neutropenia and mild thrombocytopenia. Brucella serology was strongly positive and blood cultures grew Brucella melitensis. The bacteremic episode of brucellosis was successfully treated with streptomycin, doxycyclin and ciprofloxacin at the outpatient clinic. To our knowledge, this is the first case of a naturally occurring Brucella infection complicated by Brucella bacteremia in a recipient of hematopoietic stem cell transplant. Conclusion Brucellosis may cause systemic infections, complicated bacteremias and serious morbidity in immunocompromised patients living in countries that are endemic for the infection. It should be considered as a possible cause of fever and pancytopenia in hematopoietic stem cell transplant recipients living in these geographical locations. Nevertheless, the infection is curable provided the diagnosis is made early and an appropriate antimicrobial therapy is promptly initiated.
机译:背景布鲁氏菌病是生活在感染流行地区的患者发病和死亡的重要原因。病例报告2006年4月,一名20岁的沙特男性在利雅得国王费萨尔专科医院和研究中心被诊断患有严重的再生障碍性贫血。在他成功进行了同种异体造血干细胞移植后的一百一十二天,他还出现了发热。中性粒细胞减少症和轻度血小板减少症。布鲁氏菌血清学呈强阳性,血液培养增加了布鲁氏菌。在门诊就诊成功用链霉素,强力霉素和环丙沙星治疗了布鲁氏菌病的细菌性发作。据我们所知,这是造血干细胞移植受者中自然发生的布鲁氏菌感染并发布鲁氏菌菌血症的首例病例。结论布鲁氏菌病可能在居住于感染流行国家的免疫功能低下的患者中引起全身感染,复杂的菌血症和严重的发病率。在居住在这些地理位置的造血干细胞移植受者中,应将其视为发烧和全血细胞减少的可能原因。但是,只要能够尽早诊断并迅速开始适当的抗菌治疗,这种感染就可以治愈。

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