Mature B-cell acute leukemia: a clinical, morphological, immunological, and cytogenetic study of nine cases.

Hematologic pathology Pub Date : 1991-01-01
A Hammami, W C Chan, S D Michels, V H Nassar
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Abstract

Nine patients who presented with acute lymphoid leukemia of mature B-cell phenotype without FAB-L3 morphology are discussed. All patients were male with a median age of 69 years. All patients had extensive bone marrow involvement at presentation with lymphoid leukemic cells in the peripheral blood. Six patients had extramedullary disease and 3 developed meningeal involvement sometime during the course of their illness. The leukemic cells were negative for terminal deoxynucleotidyl transferase in all 9 cases, and monoclonal surface immunoglobulin was demonstrated in all 8 cases evaluated with a lambda light chain predominance. Clonal chromosomal abnormalities were detected in 4 of 6 cases studied with no specific pattern identified, although abnormalities involving chromosome 8 were present in all 4 cases. Despite aggressive chemotherapy, only 2 patients achieved complete remission which was of short duration (1 month) in 1 patient. Eight patients died of their disease 1 week to 20 months after diagnosis with a median survival of 5.5 months. Mature B-cell acute leukemias that are not of the FAB-L3 type have a very aggressive clinical course and poor prognosis.

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成熟b细胞急性白血病:九例临床、形态学、免疫学和细胞遗传学研究。
本文讨论了9例无FAB-L3形态的成熟b细胞型急性淋巴细胞白血病患者。所有患者均为男性,中位年龄69岁。所有患者在外周血淋巴性白血病细胞出现时均有广泛的骨髓受累。6例患者有髓外病变,3例在发病过程中出现脑膜受累。9例白血病细胞末端脱氧核苷酸转移酶均为阴性,8例白血病细胞均存在单克隆表面免疫球蛋白,以lambda轻链优势进行评估。6例研究病例中有4例检测到克隆性染色体异常,但未确定具体模式,尽管所有4例病例均存在涉及8号染色体的异常。尽管有积极的化疗,只有2例患者达到完全缓解,持续时间短(1个月)。8例患者在诊断后1周到20个月死亡,中位生存期为5.5个月。非FAB-L3型的成熟b细胞急性白血病具有非常侵袭性的临床病程和不良预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Topobiology in hematopoiesis. Progress in antisense therapeutics. Ex vivo expansion of hematopoietic progenitor cells in human cord blood: an effect enhanced by cord blood serum. Lineage identification of acute leukemias: relevance of immunologic and ultrastructural techniques. Bone marrow morphology during induction phase of therapy for acute myeloid leukemia (AML).
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