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Immunophenotypic and Cytogenetic Features of Childhood Acute Leukemia in Serbia and Montenegro

机译:塞尔维亚和黑山儿童急性白血病的免疫表型和细胞遗传学特征

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摘要

Childhood acute leukemia (AL) is comprised of a heterogeneous group of diseases. The purpose of this study was to evaluate the clinical and biological features of AL in Serbia and Montenegro at presentation using inexpensive technologies. This study included 335 newly diagnosed patients enrolled at the two leading pediatric onco-hematology centers during a six-year period (1996-2002). Morphological analysis was performed using conventional methods and immunophenotyping was performed with five monoclonal antibodies (CD3, CD19, CD10, CD13 and CD33) using the alkaline-phosphatase/anti-alkaline-phosphatase (APAAP) method. Cytogenetic analysis was performed directly on bone marrow cells and/or un-stimulated cells from 24-48h cultures. The distribution ofimmunological subtypes was as follows: 240 (72%) were diagnosed with B-cell precursor acute lymphoblastic leukemia (BCP-ALL), 48 (14%) had T-ALL and 47 (14%) acute myeloid leukemia (AML). Cytogenetic analyses were performed on 193 patients and revealed164 cases of ALL and 29 cases of AML. Normal karyotype was found in 57 % of ALL and 55% of AML patients, while Cytogenetic abnormalities including structural, numerical and complex chromosomal rearrangements were found in 43 % of ALL and 45% of AML patients. Distribution of age, gender and immunophenotype were as expected for Caucasian children. This study represents the first description of the immunophenotypic and Cytogenetic characteristics of a large series of children with AL, and is representativeof the entire population of Serbia and Montenegro.
机译:儿童急性白血病(AL)由多种疾病组成。这项研究的目的是使用廉价技术评估在塞尔维亚和黑山的AL的临床和生物学特征。这项研究包括在六年期间(1996年至2002年)在两个主要的儿科肿瘤血液学中心招募的335名新诊断患者。使用常规方法进行形态分析,并使用碱性磷酸酶/抗碱性磷酸酶(APAAP)方法对五种单克隆抗体(CD3,CD19,CD10,CD13和CD33)进行免疫表型分析。细胞遗传学分析直接在来自24-48h培养的骨髓细胞和/或未刺激的细胞上进行。免疫亚型的分布如下:诊断为B细胞前体急性淋巴细胞白血病(BCP-ALL)的为240(72%),患有T-ALL的为48(14%),患有急性髓性白血病(AML)的为47(14%)。 。对193例患者进行了细胞遗传学分析,发现164例ALL和29例AML。在57%的ALL和55%的AML患者中发现了正常的核型,而在43%的ALL和45%的AML患者中发现了细胞遗传异常,包括结构,数字和复杂的染色体重排。白人儿童的年龄,性别和免疫表型分布符合预期。这项研究代表了一系列AL儿童的免疫表型和细胞遗传学特征的首次描述,并且代表了塞尔维亚和黑山的整个人口。

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