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骨髓增生异常综合征中的混合谱系嗜酸性粒细胞/嗜碱性粒细胞危象:一种罕见的进展形式。

Mixed-lineage eosinophil/basophil crisis in MDS: a rare form of progression.

作者信息

Wimazal F, Baumgartner C, Sonneck K, Zauner C, Geissler P, Schur S, Samorapoompichit P, Müllauer L, Födinger M, Agis H, Sperr W R, Valent P

机构信息

Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Austria.

出版信息

Eur J Clin Invest. 2008 Jun;38(6):447-55. doi: 10.1111/j.1365-2362.2008.01950.x. Epub 2008 Apr 24.

Abstract

BACKGROUND

Basophilic crisis and eosinophilia are well recognized features of advanced chronic myeloid leukaemia. In other myeloid neoplasms, however, transformation with marked basophilia and eosinophilia is considered unusual.

DESIGN

We examined the long-term follow-up of 322 patients with de novo myelodysplastic syndromes (MDS) to define the frequency of basophilic, eosinophilic and mixed lineage (basophilic and eosinophilic) transformation.

RESULTS

Of all patients, only one developed mixed lineage crisis (>or= 20% basophils and >or= 20% eosinophils). In this patient, who initially suffered from chronic myelomonocytic leukaemia, basophils increased to 48% and eosinophils up to 31% at the time of progression. Mixed lineage crisis was not accompanied by an increase in blast cells or organomegaly. The presence of BCR/ABL and other relevant fusion gene products (FIP1L1/PDGFRA, AML1/ETO, PML/RAR alpha, CBF beta/MYH11) were excluded by PCR. Myelomastocytic transformation/myelomastocytic leukaemia and primary mast cell disease were excluded by histology, KIT mutation analysis, electron microscopy and immunophenotyping. Basophils were thus found to be CD123+, CD203c+, BB1+, KIT- cells, and to express a functional IgE-receptor. Among the other patients with MDS examined, 4(1.2%) were found to have marked basophilia (>or= 20%) and 7(2.1%) were found to have massive eosinophilia ( >or= 20%), whereas mixed-lineage crisis was detected in none of them.

CONCLUSIONS

Mixed basophil/eosinophil crisis may develop in patients with MDS but is an extremely rare event.

摘要

背景

嗜碱性粒细胞危象和嗜酸性粒细胞增多是晚期慢性髓性白血病的公认特征。然而,在其他髓系肿瘤中,伴有显著嗜碱性粒细胞增多和嗜酸性粒细胞增多的转化被认为不常见。

设计

我们对322例初发骨髓增生异常综合征(MDS)患者进行了长期随访,以确定嗜碱性粒细胞、嗜酸性粒细胞及混合谱系(嗜碱性粒细胞和嗜酸性粒细胞)转化的频率。

结果

在所有患者中,只有1例发生了混合谱系危象(嗜碱性粒细胞≥20%且嗜酸性粒细胞≥20%)。该患者最初患有慢性粒单核细胞白血病,病情进展时嗜碱性粒细胞增至48%,嗜酸性粒细胞增至31%。混合谱系危象未伴有原始细胞增多或器官肿大。通过聚合酶链反应排除了BCR/ABL及其他相关融合基因产物(FIP1L1/PDGFRA、AML1/ETO、PML/RARα、CBFβ/MYH11)的存在。通过组织学、KIT突变分析、电子显微镜检查和免疫表型分析排除了髓肥大细胞转化/髓肥大细胞白血病和原发性肥大细胞疾病。嗜碱性粒细胞被发现为CD123+、CD203c+、BB1+、KIT-细胞,并表达功能性IgE受体。在其他接受检查的MDS患者中,4例(1.2%)有显著嗜碱性粒细胞增多(≥20%),7例(2.1%)有大量嗜酸性粒细胞增多(≥20%),但均未检测到混合谱系危象。

结论

MDS患者可能发生嗜碱性粒细胞/嗜酸性粒细胞混合危象,但极为罕见。

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