1例ph1阴性,BCR-ABL重排阳性,血液学不典型慢性髓性白血病(CML)的粒细胞异常染色质聚集。

G Tertian, M Misrahi, D Diallo, F Mielot, C Leonard, S Salmeron, G Tchernia
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引用次数: 0

摘要

在本研究中,我们报告了一例患者表现出异常染色质聚集(ACC)综合征,这是一种罕见的疾病,与骨髓增生性疾病和骨髓增生异常疾病具有相同的特征。虽然在ACC中观察到各种非特异性细胞遗传学异常,但尚未报道Ph1染色体的存在。在我们的患者中,尽管缺乏Ph1,但血液和骨髓样本的PCR分析显示BCR-ABL重排。这些结果表明,至少一些ACC综合征病例可能代表一种形式的ph1阴性慢性髓性白血病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abnormal chromatin clumping in granulocytes in a case of Ph1-negative, BCR-ABL rearrangement positive, haematologically atypical chronic myeloid leukaemia (CML).

In the present study, we report the case of a patient displaying an abnormal chromatin clumping (ACC) syndrome, a rare disease which shares features with both myeloproliferative and myelodysplastic disorders. Although various non specific cytogenetic abnormalities have been observed in ACC, the presence of a Ph1 chromosome has not been reported. In our patient, despite a lack of Ph1, PCR analysis of blood and bone marrow samples revealed a BCR-ABL rearrangement. These results indicate that at least some cases of ACC syndrome could represent a form of Ph1-negative chronic myeloid leukaemia.

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