急性早幼粒细胞白血病:接受金属阿育吠陀治疗的新生患者37年的持续生存期

B. Prakash, S. Prakash, S. Tiwari
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引用次数: 0

摘要

急性早幼粒细胞白血病(Acute promyelocytic leukemia, APML)是急性髓性白血病的一种亚型。临床表现为贫血、疲劳、虚弱、频繁感染和伴有易出血和凝血功能障碍的发热。诊断通过骨髓穿刺显示增加的早幼粒细胞和检测PML-RARα融合基因。在过去的几十年里,随着全反式维甲酸(ATRA)和三氧化二砷(ATO)的诱导,APML的治疗取得了显著的进展。这也大大降低了死亡率和复发率。同样,近90%的患者能够无病生活10年左右。然而,这些治疗存在一定的障碍,主要是由于ATRA和ATO相关的副作用、复发和有限的缓解期。这里报告一例新诊断的APML病例。该患者在阿利格尔和新德里的主要医疗中心被诊断出来,1982年在没有确定的治疗方法的情况下只接受了输血治疗。患者已经完成了37年的生存,没有任何疾病迹象和任何不良反应。该方法可作为APML的附加药物治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute Promyelocytic Leukemia: 37 Years Long Ongoing Survival in a de novo Patient with Metal-Based Ayurvedic Treatment
Abstract Acute promyelocytic leukemia (APML) is a subtype of acute myeloid leukemia. The condition is clinically marked by anemia, fatigue, weakness, frequent infections, and fever associated with easy bleeding and coagulopathy. The diagnosis is made through bone marrow aspiration exhibiting increased promyelocytes and test for PML-RARα fusion gene. There has been remarkable progress in the treatment of APML in the past few decades with the induction of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO). This has also brought down mortality and relapse rates considerably. Similarly, nearly 90% patients are able to live disease free for about 10 years. However, there are certain hindrances to these treatments majorly due to side effects, relapses, and limited periods of remission associated with ATRA and ATO. Here, a freshly diagnosed case of APML is being reported. The patient was diagnosed in leading medical centers of Aligarh and New Delhi and only treated with blood transfusions in the absence of an established line of treatment in 1982. The patient has completed 37 years long survival without any sign of the disease and any adverse effect. This approach could be considered as an add-on medical therapy for APML.
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