Uğur Bilgin Aynur, Karaselek Mehmet Ali, Bilgin Rasim
Department of Hematology, Meram Medical School, Necmettin Erbakan University, Konya, Turkey.
Department of Hematology, Meram Medical School, Necmettin Erbakan University, Konya, Turkey.
Transfus Apher Sci. 2015 Apr;52(2):214-6. doi: 10.1016/j.transci.2015.01.001. Epub 2015 Jan 8.
Immune thrombocytopenia (ITP) is an acquired immune-mediated disease characterized by persistant thrombocytopenia. Onset of the disease and the clinical course is highly variable, but the disease typically has a benign course. Patients rarely develop serious life-threatening bleeding. Herein, a case with refractory ITP and massive alveolar hemorrhage who was successfully treated with a fast and sequential approach is presented for the first time.
免疫性血小板减少症（ITP）是一种获得性免疫介导的疾病，其特征为持续性血小板减少。该疾病的起病和临床病程高度可变，但通常呈良性病程。患者很少发生严重的危及生命的出血。在此，首次报告了一例难治性ITP合并大量肺泡出血的病例，该病例采用快速序贯治疗方法成功治愈。
