Two Cases of Autoimmune Hemolytic Anemia Secondary to Brucellosis: A Review of Hemolytic Disorders in Patients with Brucellosis

被引:15
作者
Eskazan, Ahmet Emre [1 ]
Dal, Mehmet Sinan [2 ]
Kaya, Safak [3 ]
Dal, Tuba [4 ]
Ayyildiz, Orhan [2 ]
Soysal, Teoman [1 ]
机构
[1] Istanbul Univ, Cerrahpasa Fac Med, Dept Internal Med, Div Hematol, Istanbul, Turkey
[2] Dicle Univ, Fac Med, Dept Internal Med, Div Hematol, Diyarbakir, Turkey
[3] Diyarbakir Training & Res Hosp, Dept Infect Dis, Diyarbakir, Turkey
[4] Dicle Univ, Fac Med, Dept Microbiol & Clin Microbiol, Diyarbakir, Turkey
关键词
brucellosis; hemolysis; anemia; thrombotic thrombocytopenic purpura; Coombs; rituximab; THROMBOTIC THROMBOCYTOPENIC PURPURA;
D O I
10.2169/internalmedicine.53.0936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Brucellosis is a worldwide zoonotic disease associated with hemolytic complications, including thrombotic microangiopathy (TMA) and hemolytic anemia. Autoimmune hemolytic anemia (AIHA) is a rare clinical presentation of this disease. In this report, we describe the cases of two patients with brucellosis who presented with Coombs-positive AIHA. We also include a review of the literature on the hemolytic complications of brucellosis. Both patients were successfully treated with a combination of doxycycline and rifampicin in addition to steroids. In the medical literature, there are several cases of TMA associated with brucellosis, although only a few cases of Coombs test-positive AIHA have been reported. Antibiotic therapy is the mainstay of treatment, and the selection of antibiotics and duration of treatment do not differ between brucellosis patients with and without hemolysis. Although rare, the potential for brucellosis should always be kept in mind in patients who present with hemolysis, especially those living in areas where brucellosis is endemic.
引用
收藏
页码:1153 / 1158
页数:6
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