Ozkalemkas Fahir, Ali Ridvan, Ozkocaman Vildan, Ozcelik Tulay, Ozkan Atilla, Tunali Ahmet
Department of Hematology, Uludag University, 16059 Gorukle, Bursa, Turkey.
Transfus Apher Sci. 2007 Feb;36(1):109-15. doi: 10.1016/j.transci.2006.05.020. Epub 2007 Feb 8.
Thrombotic thrombocytopenic purpura (TTP) is a classic, but not a common disorder of hematology. Plasma exchange (PE) was shown to nearly reverse its 90% mortality rate. However, there are still some fatal outcomes in this dramatic disease. We present our experience of plasma exchange plus corticosteroids for the treatment of TTP in our hospital. Patients with TTP diagnosed between January 1996 and January 2005 were identified by a retrospective review of records of the Uludag University Hospital, Bursa (the largest referral center for adults with this disorder in this region with an estimated 2.2 million residents), which performs all therapeutic PE in the southern Marmara region in Turkey. A total of 11 (6 male, 5 female) patients were treated for TTP during this period. The median age was 39 years (range 18-49). One plasma volume exchange daily plus steroid was the principle treatment in all patients. A total of 295 PE sessions were performed. We have obtained six complete responses (CR) and three partial responses (PR) with daily PE and steroid (response rate 9/11). One of our primary refractory patients was saved with pulse steroid+cyclosporine+vincristine. Now, he is disease free for over one year. The other refractory patient did not develop any response to salvage therapy and expired on day 15 with status epilepticus and ventilator related pneumonia (mortality rate 1/11). A CR was obtained with adjuvant treatments in all three PR patients. Only one CR patient developed an early relapse (early relapse rate in CR patients 1/6). She was treated successfully with daily PE plus vincristine. Our median follow up period was 25 months (range 9-108). Considering our local population, our annual incidence is only about 0.63 new cases per one million people. This figure is considerably less than the data from US, which indicated an incidence of 3.7 cases per 1,000,000. To our knowledge, there is no high variability in the incidence of TTP in the different geographical regions of the world. It suggests that considerable number of patients escaped notice. We hope that, demonstrating the successful outcome, this article serves to urge primary physicians to keep in mind the diagnosis of TTP and refer suspected cases quickly.
血栓性血小板减少性紫癜(TTP)是一种典型但并不常见的血液系统疾病。血浆置换(PE)已被证明能使该病近90%的死亡率几乎得到逆转。然而,在这种严重疾病中仍存在一些致命的结局。我们介绍我院采用血浆置换联合皮质类固醇治疗TTP的经验。通过回顾布尔萨乌鲁达大学医院(土耳其马尔马拉地区南部最大的成人该疾病转诊中心,该地区约有220万居民)1996年1月至2005年1月期间的记录,确定了TTP患者。在此期间,共有11例(6例男性,5例女性)患者接受了TTP治疗。中位年龄为39岁(范围18 - 49岁)。所有患者的主要治疗方法是每天进行一次血浆量置换并联合使用类固醇。共进行了295次血浆置换治疗。通过每日血浆置换和类固醇治疗,我们获得了6例完全缓解(CR)和3例部分缓解(PR)(缓解率9/11)。我们的一名原发性难治性患者通过脉冲类固醇 + 环孢素 + 长春新碱得以挽救。现在,他已无病生存超过一年。另一名难治性患者对挽救治疗无反应,于第15天因癫痫持续状态和呼吸机相关性肺炎死亡(死亡率1/11)。所有3例部分缓解患者通过辅助治疗均获得了完全缓解。只有1例完全缓解患者出现早期复发(完全缓解患者的早期复发率1/6)。她通过每日血浆置换联合长春新碱治疗成功。我们的中位随访期为25个月(范围9 - 108个月)。考虑到我们当地的人口数量,我们的年发病率仅约为每百万人0.63例新病例。这个数字远低于美国的数据,美国的数据显示发病率为每100万人3.7例。据我们所知,世界不同地理区域TTP的发病率没有很大差异。这表明有相当数量的患者未被发现。我们希望通过展示成功的治疗结果,本文能促使基层医生牢记TTP的诊断,并迅速转诊疑似病例。