Case Report
Acute Brucellosis Presenting as an Autoimmune Hemolytic Anemia
Table 1
Clinical and demographic characteristics of reported hemolytic complications in brucellosis.
| First author; year of publication | Country | Number of cases | Age/gender | Hematological disease | Treatment |
| Kiki et al. [6]; 2008 | Turkey | 1 | 19 yr, female | TTP | Doxycycline, rifampicin, plasma exchange | Wehbe and Moore [7]; 2008 | United States | 1 | 34 yr, female | AIHA | No immunosuppressant | Sari et al. [10]; 2008 | Turkey | 1 | 26 yr, female | AIHA | Corticosteroids | Bourantas et al. [8]; 2010 | Greece | 1 | 79 yr, female | AIHA | Corticosteroids, rituximab | Apa et al. [11]; 2013 | Turkey | 1 | 5-month infant | AIHA | Rifampicin, trimethoprim/sulfamethoxazole Blood transfusion, corticosteroids | Eskazan et al. [9]; 2014 | Turkey | 2 | 72 yr, male; 50 yr, female | AIHA | Doxycycline, rifampicin, corticosteroids | Tunccan et al. [4]; 2014 | Turkey | 1 | 75 yr, male | ITP | Doxycycline, rifampicin, corticosteroids | Makis et al. [3]; 2017 | Greece | 1 | 5.5 yr female | ITP | Rifampicin, trimethoprim/sulfamethoxazole (TMP/SMX), IV IG |
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AIHA = autoimmune hemolytic anemia; TTP = thrombotic thrombocytopenic purpura; ITP = immune thrombocytopenic purpura.
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