Characteristics of Chronic Lymphocytic Leukemia in Sudanese Patients

Ameen Abdulaziz Basabaeen, E. Abdelgader, Ebtihal Ahmed Babekir, N. Abdelateif, Sadia Osman Abdelrahim, O. Altayeb, E. Fadul, H. Osman, Salem Ahmed Bamusa, Ibrahim Khider Ibrahim
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Abstract

Objective: Our study aimed to characterize clinical, hematological and Immunophenotyping patterns in Sudanese patients with Chronic Lymphocytic Leukemia. Methods: A cross-sectional study was conducted in Khartoum state, Sudan, during the period from April 2017 to April 2018, involved 110 CLL patients. Physical examination, Complete Blood Count and Immunophenotyping were performed for all patients to confirm the diagnosis. Clinical staging such as Rai and Binet stages were applied. The statistical analysis was performed by using SPSS version 23.0. Results: In this study, 71.8% were males and 28.2% were females. Lymphadenopathy, splenomegaly, hepatomegaly, leukocytosis, thrombocytopenia, and anemia were seen in 71%, 49%, 13%, 60.9%, 39% and 34.5% of patients respectively. However, about 90% of patients displayed an advanced Rai risk stage and 70% were at Binet stage B or C. All CLL samples expressed CD45, CD19 and CD20. All the CLL cases were negative for the T-cell marker CD3.CD5 was expressed in 80% patients; CD23 was expressed in 92.7% patients. CD22, CD79b and FMC7 were negative in 91.8%, 77.3%, and 96.4% of patients respectively. Conclusions: CLL in Sudan is a disease of the elderly and more frequently in males than females. The incidence at young patients was higher than those reported by Western studies. Most of our patients presented advanced Rai and Binet stages. CD22 may be a highly specific marker for diagnosing CLL in Sudanese patients and should be included in all diagnostic panels used to differentiate CLL from other B cell lymphoproliferative disorders in Sudan.
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苏丹慢性淋巴细胞白血病的特点
目的:我们的研究旨在描述苏丹慢性淋巴细胞白血病患者的临床、血液学和免疫表型特征。方法:2017年4月至2018年4月期间,在苏丹喀土穆州进行了一项横断面研究,涉及110名CLL患者。所有患者均行体格检查、全血细胞计数和免疫分型以确认诊断。临床分期如Rai和Binet分期。采用SPSS 23.0版本进行统计分析。结果:本组患者中男性占71.8%,女性占28.2%。淋巴结肿大、脾肿大、肝肿大、白细胞增多、血小板减少、贫血分别占71%、49%、13%、60.9%、39%和34.5%。然而,约90%的患者表现为晚期Rai风险期,70%为Binet B期或c期。所有CLL样本均表达CD45、CD19和CD20。所有CLL病例的t细胞标志物CD3均为阴性。CD5在80%的患者中表达;92.7%的患者表达CD23。CD22、CD79b和FMC7分别为91.8%、77.3%和96.4%的患者阴性。结论:在苏丹,CLL是一种老年疾病,男性多于女性。年轻患者的发病率高于西方研究报告的发病率。我们的大多数患者表现为晚期Rai和Binet期。CD22可能是诊断苏丹患者CLL的高度特异性标志物,应包括在苏丹用于区分CLL与其他B细胞淋巴增生性疾病的所有诊断面板中。
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