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慢性嗜中性粒细胞白血病的克隆性证据。

Evidence of clonality in chronic neutrophilic leukaemia.

作者信息

Böhm J, Kock S, Schaefer H E, Fisch P

机构信息

Department of Pathology, University of Freiburg, Medical School, D-79002 Freiburg, Germany.

出版信息

J Clin Pathol. 2003 Apr;56(4):292-5. doi: 10.1136/jcp.56.4.292.

Abstract

BACKGROUND

Chronic neutrophilic leukaemia (CNL) is a rare myeloproliferative disorder of elderly patients characterised by sustained neutrophilia and splenomegaly. The diagnosis of CNL requires the exclusion of BCR/ABL positive chronic myelogenous leukaemia (CML) and of leukaemoid reactions (LRs). The differentiation between CNL and LR is problematic because both conditions share similar morphological features; it is also important because patients with CNL generally have a poor prognosis.

AIMS

To determine whether CNL and LR could be distinguished on the basis of different clonality patterns.

METHODS

Blood samples from 52 women were studied using the human androgen receptor gene assay (HUMARA).

RESULTS

Monoclonality was found in the neutrophils in all 17 patients with different myeloproliferative syndromes (MPSs), including those with CNL. In four of the patients with CNL, autologous T cells were also monoclonal, suggesting that they belonged to the neoplastic clone. This finding was in contrast to other MPSs in which T cells were almost always polyclonal. Of nine patients with clinically suspected LR, the neutrophils of five were polyclonal, whereas three patients had monoclonal neutrophils, suggesting that they might be in the process of developing an MPS. Among 26 healthy blood donors, 20 had polyclonal neutrophils and five showed skewed clonality patterns. One case of LR and one normal blood donor were scored "not informative" at the HUMARA locus.

CONCLUSIONS

Clonality studies of blood neutrophils using HUMARA aid in distinguishing female patients with monoclonal CNL from those with LR. For the diagnosis of CNL, monoclonality of the neutrophils should be demonstrated whenever possible.

摘要

背景

慢性中性粒细胞白血病(CNL)是一种罕见的老年骨髓增殖性疾病,其特征为持续性中性粒细胞增多和脾肿大。CNL的诊断需要排除BCR/ABL阳性慢性粒细胞白血病(CML)和类白血病反应(LR)。CNL与LR的鉴别诊断存在问题,因为这两种情况具有相似的形态学特征;这一点也很重要,因为CNL患者的预后通常较差。

目的

确定是否可以根据不同的克隆模式区分CNL和LR。

方法

使用人类雄激素受体基因检测(HUMARA)对52名女性的血液样本进行研究。

结果

在所有17例不同骨髓增殖综合征(MPS)患者中,包括CNL患者,中性粒细胞均发现单克隆性。在4例CNL患者中,自体T细胞也是单克隆的,表明它们属于肿瘤克隆。这一发现与其他MPS不同,在其他MPS中T细胞几乎总是多克隆的。在9例临床疑似LR的患者中,5例患者的中性粒细胞是多克隆的,而3例患者的中性粒细胞是单克隆的,这表明他们可能正处于发展为MPS的过程中。在26名健康献血者中,20人的中性粒细胞是多克隆的,5人显示克隆模式偏斜。1例LR患者和1名正常献血者在HUMARA位点的检测结果为“无信息”。

结论

使用HUMARA对血液中性粒细胞进行克隆性研究有助于区分单克隆CNL女性患者和LR患者。对于CNL的诊断,应尽可能证明中性粒细胞的单克隆性。

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