Juliusson G, Ost A, Biberfeld P, Robèrt K H
Acta Pathol Microbiol Immunol Scand A. 1986 Mar;94(2):133-9.
A 56-year old man with a Rai stage IV B-cell chronic lymphocytic leukaemia (polymorphic immunocytoma according to the Kiel classification) of mu kappa-phenotype with a clonal chromosomal abnormality in cells from peripheral blood, bone marrow, and spleen is reported on. Following splenectomy (without further therapy) the blood lymphocytosis gradually decreased to normal and the patient entered a remission, assigned 42 months after splenectomy by immunological and cytogenetic studies that revealed no cells of clonal origin in blood or bone marrow. Utilizing cellular markers of clonality, we thus confirm that haematological remissions may follow splenectomy. A subsequently developed orbital lymphoma (without leukaemia) consisted of tumor cells derived from the initial leukaemia cell clone as indicated by their immune and cytogenetic phenotype. The case report is discussed in relation to previous reports on "spontaneous" remissions of lymphoid leukaemias.
报告了一名56岁男性,患有Rai IV期B细胞慢性淋巴细胞白血病(根据基尔分类为多形性免疫细胞瘤),呈μκ表型,外周血、骨髓和脾脏细胞存在克隆性染色体异常。脾切除术后(未进行进一步治疗),血液淋巴细胞增多症逐渐降至正常,患者进入缓解期,脾切除术后42个月通过免疫和细胞遗传学研究确定缓解,研究显示血液或骨髓中无克隆起源的细胞。利用克隆性细胞标志物,我们因此证实脾切除术后可能出现血液学缓解。随后发生的眼眶淋巴瘤(无白血病)由最初白血病细胞克隆衍生的肿瘤细胞组成,其免疫和细胞遗传学表型表明了这一点。结合先前关于淋巴细胞白血病“自发”缓解的报告对该病例报告进行了讨论。