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高危骨髓增生异常综合征与慢性淋巴细胞白血病共存9年以上:淋巴克隆对髓系克隆的抑制作用?

High risk myelodysplastic syndrome coexistent with chronic lymphocytic leukemia for more than 9 years: inhibition of the myeloid clone by the lymphoid clone?

作者信息

Bastion Y, Thomas X, Felman P, Campos L, Charrin C, Coiffier B

机构信息

Hematology Service, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France.

出版信息

Leukemia. 1991 Nov;5(11):1006-9.

PMID:1961029
Abstract

We describe a patient in whom the concomitant diagnosis of refractory anemia with excess of blasts (16% on initial marrow examination) and chronic lymphocytic leukemia was made more than 9 years ago. The myeloid clone showed a complex karyotypic abnormality. Evolution has so far been remarkably stable, without transformation into acute leukemia. Clonogenic assays showed that patient's serum inhibited the patient's own granulocyte-macrophage colony-forming units (CFU-GM). This inhibition was also present for a control subject's CFU-GM and acute myeloid leukemia clonogenic cells. This raises the problem of a down-regulation of the myeloid clone by the malignant lymphoid clone in this patient, and the possible mechanisms for this are discussed.

摘要

我们描述了一位患者,9年多前该患者被同时诊断为难治性贫血伴原始细胞增多(初始骨髓检查时原始细胞占16%)和慢性淋巴细胞白血病。髓系克隆显示出复杂的核型异常。迄今为止,病情进展一直非常稳定,未转化为急性白血病。集落形成试验显示,患者血清抑制了患者自身的粒-巨噬细胞集落形成单位(CFU-GM)。这种抑制作用在对照受试者的CFU-GM和急性髓系白血病集落形成细胞中也存在。这就提出了该患者中恶性淋巴系克隆对髓系克隆进行下调的问题,并对其可能机制进行了讨论。

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