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 publicationCountryNumber of casesAge/genderHematological diseaseTreatment

Kiki et al. [6]; 2008Turkey119 yr, femaleTTPDoxycycline, rifampicin, plasma exchange
Wehbe and Moore [7]; 2008United States134 yr, femaleAIHANo immunosuppressant
Sari et al. [10]; 2008Turkey126 yr, femaleAIHACorticosteroids
Bourantas et al. [8]; 2010Greece179 yr, femaleAIHACorticosteroids, rituximab
Apa et al. [11]; 2013Turkey15-month infantAIHARifampicin, trimethoprim/sulfamethoxazole Blood transfusion, corticosteroids
Eskazan et al. [9]; 2014Turkey272 yr, male; 50 yr, femaleAIHADoxycycline, rifampicin, corticosteroids
Tunccan et al. [4]; 2014Turkey175 yr, maleITPDoxycycline, rifampicin, corticosteroids
Makis et al. [3]; 2017Greece15.5 yr femaleITPRifampicin, trimethoprim/sulfamethoxazole (TMP/SMX), IV IG

AIHA = autoimmune hemolytic anemia; TTP = thrombotic thrombocytopenic purpura; ITP = immune thrombocytopenic purpura.