儿童急性淋巴细胞白血病:马里12例。

B Togo, F Traoré, A A Diakité, S Diallo, B Traoré, O Fenneteau, A Touré, F Traoré-Dicko, M Sylla, T Sidibé, G Leverger
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引用次数: 0

摘要

儿童急性淋巴细胞白血病是工业化国家最常见的儿童恶性肿瘤,在非洲出版物中很少有关于它的数据。本前瞻性单中心研究的目的是评估在马里巴马科Gabriel tour教学医院儿科肿瘤科接受淋巴细胞白血病治疗的儿童的社会人口统计学、临床和实验室特征。患者和方法:本研究包括2007年1月1日至2009年9月30日期间因细胞学记录的急性淋巴细胞白血病接受治疗的所有1至15岁儿童。结果:研究期间共治疗12例,其中男8例,女4例(性别比例2例)。平均年龄92个月。2例年龄小于4岁。5例(41.7%)为5 ~ 9岁,5例(41.7%)为10 ~ 15岁。发病时,9例(75%)患者处于恶病质状态;淋巴结肿大、脾肿大、肝肿大10例;其中2人有神经系统疾病。确诊延迟5个月4例(33.3%),其余病例延迟不到5个月。初始白细胞计数大于50 000/mm3者10例,小于50 000/mm3者2例。所有患者均采用LAL GFAOP方案治疗,其中LAL1 6例,LAL2 5例,LAL3 1例。治疗并发症包括6例无证感染,2例出血,4例重度贫血。4名患者死亡。随访5年,总生存率为66.7%。结论:需要一项包括更多儿童的多中心研究来增加对撒哈拉以南非洲儿童急性淋巴细胞白血病特征的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Childhood acute lymphoblastic leukemia: 12 cases in Mali].

Introduction: Data about childhood acute lymphoblastic leukemia, the most common childhood malignancy in industrialized countries, are scarce in African publications. The purpose of this prospective, unicentric study were to assess the socio-demographic, clinic and laboratory characteristics of the children treated for lymphoblastic leukemia in our pediatric oncology unit in Gabriel Touré Teaching Hospital in Bamako, Mali.

Patients and methods: This study includes all children between 1 and 15 years old treated for cytologically documented acute lymphoblastic leukemia from January 1, 2007 to September 30, 2009.

Results: A total of 12 cases including 8 boys and 4 girls (sex ration, 2) were treated during the study period. Mean age was 92 months. Age was less than 4 years old in 2 cases. 5 (41,7%) were between 5 and 9 years in 5 (41.7%) and between 10 to 15 years in five. At the time of presentation, 9 patients (75%) were in a cachectic state; 10 had lymphadenopathies, splenomegaly and hepatomegaly; and 2 had neurological involvement. The delay for definitive diagnosis was 5 months in 4 cases (33,3 %) and less than 5 months in the remaining cases. Initial white blood cell count was more than 50 000/mm3 in 10 cases and less less than 50 000/mm3 in 2 cases. All patients were treated using the LAL GFAOP protocol including LAL1 in 6 cases, LAL2 in 5 and LAL3 in 1. Treatment complications were included 6 undocumented infections in 6 cases, hemorrhage in 2 and severe anemia in 4. Four patients died. At 5 years follow-up, overall survival rate was 66,7%.

Conclusion: A multicentric study including a greater number of children is needed to increase understanding of the characteristics of childhood acute lymphoblastic leukemia in sub-Saharan Africa.

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