Altuntas Fevzi, Yildiz Orhan, Sari Ismail, Eser Bulent, Cetin Mustafa, Unal Ali
Department of Hematology, Erciyes University, Faculty of Medicine, Kayseri, Turkey.
Am J Hematol. 2005 Nov;80(3):204-6. doi: 10.1002/ajh.20386.
Severe thrombocytopenia is a rare hematologic manifestation of brucellosis, which can occasionally be associated with bleeding into the skin and from mucosal sites. Prompt recognition of this brucellosis complication and aggressive therapy is vital because the mortality rate associated with bleeding into the central nervous system is high. We report a case of a patient infected with Brucella melitensis who was admitted with a severe case of thrombocytopenic purpura. The patient responded well to intravenous gamma globulin (IVIg) treatment with platelet recovery within 2-3 days. For cases of Brucella-induced thrombocytopenic purpura, IVIg may be administered as an urgent therapy until the microbial therapy takes effect.
严重血小板减少症是布鲁氏菌病罕见的血液学表现,偶尔可伴有皮肤及黏膜部位出血。及时识别这种布鲁氏菌病并发症并积极治疗至关重要,因为中枢神经系统出血相关的死亡率很高。我们报告一例感染羊种布鲁氏菌的患者,该患者因严重血小板减少性紫癜入院。患者对静脉注射丙种球蛋白(IVIg)治疗反应良好,血小板在2 - 3天内恢复。对于布鲁氏菌引起的血小板减少性紫癜病例,在微生物治疗起效前,可将IVIg作为紧急治疗药物使用。