Kurtaran Behice, Oto Ozgur Akin, Candevir Aslihan, Inal Ayse Seza, Sirin Yusuf
Indian J Hematol Blood Transfus. 2011 Mar;27(1):35-8. doi: 10.1007/s12288-010-0049-8. Epub 2011 Feb 4.
To report a case of HIV infection presenting with thrombotic thrombocytopenic purpura (TTP) and brucellosis that responded well to plasmapheresis and anti-infective therapy. A 64-year-old woman with moderate confusion, fever and pancytopenia was admitted. HIV infection history was taken from her family and she was not receiving antiretroviral therapy last one year. She had generalized purpuric skin lesions. Wright tube agglutination test was found positive with a 1:160 dilution and the patient was diagnosed as brucellosis. Detailed literature search showed brucellosis as a possible cause of TTP. Patient was treated by plasma exchange/fresh frozen plasma and antimicrobials and the response was excellent. Although brucellosis seems to explain the clinical picture of this patient, it is revealed that broad differential diagnosis is needed to reach uncommon diagnosis like TTP particularly in HIV infected patients.
报告一例表现为血栓性血小板减少性紫癜(TTP)和布鲁氏菌病的HIV感染病例,该病例对血浆置换和抗感染治疗反应良好。一名64岁女性因中度意识模糊、发热和全血细胞减少入院。从其家人处了解到HIV感染史,且她在过去一年未接受抗逆转录病毒治疗。她有全身性紫癜性皮肤病变。wright试管凝集试验在1:160稀释度时呈阳性,该患者被诊断为布鲁氏菌病。详细的文献检索显示布鲁氏菌病是TTP的可能病因。患者接受了血浆置换/新鲜冰冻血浆和抗菌药物治疗,反应良好。虽然布鲁氏菌病似乎可以解释该患者的临床表现,但结果显示,对于像TTP这样的罕见诊断,尤其是在HIV感染患者中,需要进行广泛的鉴别诊断。