Kiki Ilhami, Gundogdu Mehmet, Albayrak Bulent, Bilgiç Yilmaz
Atatürk University Medical Faculty, Department of Internal Medicine, Erzurum, Turkey.
Am J Med Sci. 2008 Mar;335(3):230-2. doi: 10.1097/MAJ.0b013e3180d09f19.
Thrombotic thrombocytopenic purpura (TTP) is characterized by disseminated thrombotic occlusions located in the microcirculation and a syndrome of microangiopathic hemolytic anemia (MAHA), thrombocytopenia, fever, and renal and neurologic abnormalities. Although several factors such as viral and bacterial pathogens, pancreatitis, drugs, collagen-vascular diseases, cancers, and pregnancy have been reported to be associated with TTP, brucellosis is an exceptional cause of this disorder. We represent a 19-year-old woman applying to our outpatient department with the complaints of headache, fever, sweat, malaise, and jaundice. Clinical signs and laboratory findings were consistent with TTP. Brucella agglutination was found to be 1/320 positive. After the administration of therapeutic plasma exchange, all symptoms and laboratory abnormalities improved dramatically. Antibiotic therapy directed to Brucella infection was initiated and no recurrence of TTP was seen.
血栓性血小板减少性紫癜(TTP)的特征是微循环中出现弥漫性血栓性阻塞以及微血管病性溶血性贫血(MAHA)、血小板减少、发热、肾脏和神经异常综合征。尽管有报道称病毒和细菌病原体、胰腺炎、药物、胶原血管疾病、癌症和妊娠等多种因素与TTP有关,但布鲁氏菌病是这种疾病的一个特殊病因。我们报告一名19岁女性,因头痛、发热、出汗、不适和黄疸前来我院门诊就诊。临床体征和实验室检查结果与TTP相符。布鲁氏菌凝集试验结果为1/320阳性。给予治疗性血浆置换后,所有症状和实验室异常均显著改善。开始针对布鲁氏菌感染进行抗生素治疗,未再出现TTP复发。