来自分子遗传学和细胞遗传学分析的证据表明骨髓组织病理学在慢性骨髓增生性疾病的诊断中是可靠的。

M Werner, V Kaloutsi, F Kausche, T Buhr, A Georgii
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引用次数: 3

摘要

通过将组织学结果与ph1易位的分子遗传学和细胞遗传学分析相关联,评估慢性骨髓增生性疾病(CMPD)患者骨髓标本的组织病理学诊断的可靠性。m-bcr重排仅在组织学诊断为慢性髓性白血病(CML)的患者(28/30)中检测到。这一发现得到了24/26 CML患者中ph1染色体存在的支持。其他类型的CMPD,包括真性红细胞增多症(PV)、原发性血小板增多症(PTH)和慢性巨核细胞-粒细胞性脊髓症(CMGM),以及无法分类的CMPD (CMPD. uc)患者均为ph 1阴性(n = 38)。对于骨髓纤维化合并CML、CMGM和CMPD的患者,CML与ph1阴性CMPD的组织病理学区分也是可靠的。结果表明,骨髓组织病理学可以可靠地诊断CML。这与血液学数据相反,如高血小板计数,在各种形式的CMPD中显示出相当大的重叠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence from molecular genetic and cytogenetic analyses that bone marrow histopathology is reliable in the diagnosis of chronic myeloproliferative disorders.

The reliability of histopathological diagnosis in bone marrow specimens from patients with chronic myeloproliferative disorders (CMPD) was evaluated by correlating the histological findings with molecular genetic and cytogenetic analyses of the Ph1-translocation. A rearrangement of m-bcr was detected only in patients (28/30) diagnosed histologically as chronic myeloid leukemia (CML). This finding was supported by the presence of a Ph1-chromosome in 24/26 patients with CML examined. All the patients with other types of CMPD, including polycythemia vera (PV), primary thrombocythemia (PTH) and chronic megakaryocytic-granulocytic myelosis (CMGM), as well as those with unclassifiable CMPD (CMPD.UC) were Ph1-negative (n = 38). The histopathological discrimination of CML from Ph1-negative varieties of CMPD was also reliable for patients with myelofibrosis complicating CML, CMGM and CMPD.UC. The results demonstrate that bone marrow histopathology allows a reliable diagnosis of CML. This is in contrast with hematological data such as high platelet counts which show considerable overlapping in the various forms of CMPD.

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