Sultan Sadia, Zaheer Hasan Abbas, Irfan Syed Mohammed, Ashar Sana
Department of Hematology and Blood Bank, Liaquat National Hospital and Medical College, Karachi, Pakistan E-mail :
Asian Pac J Cancer Prev. 2016;17(1):369-72. doi: 10.7314/apjcp.2016.17.1.369.
Acute myeloid leukemia is an acquired clonal heterogeneous stem cell disorder. Hence, various parameters are sought out to categorize this disease into subtypes, so that as a consequence specific treatment modalities can be offered. Conventionally, the practically used method for classification utilizes French American British (FAB) criteria based on morphology and cytochemistry. The aim of present study was to determine the current spectrum of AML sub types in patients in Karachi.
This single centre cross sectional study was conducted at Liaquat National Hospital, Karachi, extending from January 2010 to December 2014. Data were retrieved from archives were analyzed with SPSS version 22.
A total of 125 patients were diagnosed at our institution with de novo AML during five years period, 76 males and 49 females. Median age was 34.5 years. AML-M1 was the predominant FAB subtype (23.2%) followed by M2 (18.4%), M3 and M4 (16% each), M0 (14.4%), M5 (7.2%), M6 (3.2%) and M7 (1.6%).
AML in Pakistani patients is seen in a relatively young population. The most common FAB subtype observed in our study was acute myeloblastic leukemia, without maturation (M1).
急性髓系白血病是一种获得性克隆性异质性干细胞疾病。因此,人们寻找各种参数将这种疾病分类为不同亚型,以便能够提供特定的治疗方式。传统上,实际使用的分类方法是采用基于形态学和细胞化学的法美英(FAB)标准。本研究的目的是确定卡拉奇患者中急性髓系白血病亚型的当前谱。
这项单中心横断面研究在卡拉奇的利亚卡特国家医院进行,时间从2010年1月至2014年12月。从档案中检索数据,并用SPSS 22版进行分析。
在五年期间,我们机构共诊断出125例初发急性髓系白血病患者,其中男性76例,女性49例。中位年龄为34.5岁。AML-M1是主要的FAB亚型(23.2%),其次是M2(18.4%)、M3和M4(各16%)、M0(14.4%)、M5(7.2%)、M6(3.2%)和M7(1.6%)。
巴基斯坦患者中的急性髓系白血病在相对年轻的人群中出现。我们研究中观察到的最常见FAB亚型是急性髓细胞白血病,无成熟型(M1)。