分化综合症;急性早幼粒细胞白血病atra /ATO诱导治疗

Q4 Medicine
Kanwal Karim, Simab Pervaiz, Ina Abdul Majeed, Sana Mushtaq, Hina Arshad
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引用次数: 0

摘要

急性早幼粒细胞白血病(APL)是一种被描述为明确的形态学和细胞遗传学异常的疾病,可导致凝血功能障碍,使患者处于危及生命的状态。15和17条染色体的特异性易位导致视黄酸受体-α (RARα)和早幼粒细胞白血病(PML)基因融合,产生异常基因突变,形成致癌蛋白PML-RARα。那些接受全反式维甲酸(ATRA)或三氧化二砷(ATO)治疗的APL患者通常会导致一种称为分化综合征的复杂情况,这种情况很少严重。本病例报告解释了一位37岁男性,诊断为急性早幼粒细胞白血病,在开始全反式维甲酸和三氧化二砷诱导治疗后出现分化综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentiation Syndrome; Post-ATRA/ATO Induction Therapy in Acute Promyelocytic Leukemia
Acute promyelocytic leukemia (APL) is a disease described as definite morphological and cytogenetical abnormalities and leads to coagulopathy leaving the patient in a life-threatening condition. A specific chromosomal translocation of 15 and 17 chromosomes leads to retinoic acid receptor-α (RARα) and promyelocytic leukemia (PML) genes fusion that produces an abnormal gene mutation forming an oncogenic protein which is (PML-RARα). Those APL patients, who have been treated with all-trans retinoic acid (ATRA) or arsenic trioxide (ATO) commonly lead a complicated condition called differentiation syndrome which is rarely severe. This case report explains the 37-years old male diagnosed with acute promyelocytic leukemia and later developed a differentiation syndrome after initiation of all-trans retinoic acid and arsenic trioxide induction therapy.
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来源期刊
Pakistan Journal of Medical & Health Sciences
Pakistan Journal of Medical & Health Sciences MEDICINE, GENERAL & INTERNAL-
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期刊介绍: Pakistan Journal of Medical and Health Sciences is an international biomedical journal from Pakistan. We publish materials of interest to the practitioners and scientists in the broad field of medicine. Articles describing original qualitative, quantitative, human/animal clinical or laboratory studies are considered for publication.
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