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骨髓的多倍体现象。

Polyploidy of the bone marrow.

作者信息

Borgström G H, Vuopio P, De la Chapelle A

出版信息

Scand J Haematol. 1976 Aug;17(2):123-31. doi: 10.1111/j.1600-0609.1976.tb01165.x.

Abstract

In a consecutive series of 841 patients whose bone marrows were cytogenetically investigated because of verified or suspected haematological disease, 11 patients were found to have at least 10% polyploid bone marrow mitoses. The chromosome numbers varied greatly between the cells of the same patients and between the patients. In 4 cases, the number was nearly or exactly tetraploid and in 1 patient a prevalent octaploid line was seen. Structurally abnormal marker chromosomes were seen in 8 of the patients. A total of 31 bone marrow chromosome counts were performed on a young woman with acute myelomonocytic leukaemia who had had several drug-induced remissions during the 3 1/2 years of disease. The results were related to the clinical findings. On several occasions a clear-cut correlation was noted between high proportions (nearly 100%) of polyploid cells and relapse on the one hand and low proportions (as low as 0%) of polyploids and remission on the other. Of the 11 patients, 2 had chronic myeloid leukaemia, 3 acute myelomonocytic leukaemia, 3 acute myeloid leukaemia and a further 3 some other malignant haematological disorders. We conclude that polyploidy is a feature associated with rare cases of leukaemia and other malignant diseases. It is often a sign of a poor prognosis.

摘要

在一组因确诊或疑似血液系统疾病而接受骨髓细胞遗传学检查的841例连续患者中,发现11例患者的骨髓有丝分裂中至少10%为多倍体。同一患者的细胞之间以及不同患者之间,染色体数目差异很大。4例患者的染色体数目接近或恰好为四倍体,1例患者可见一条占优势的八倍体线。8例患者可见结构异常的标记染色体。对一名患有急性粒单核细胞白血病的年轻女性进行了总共31次骨髓染色体计数,该患者在患病3年半期间有几次药物诱导的缓解。结果与临床发现相关。有几次,一方面多倍体细胞比例高(接近100%)与复发之间,另一方面多倍体细胞比例低(低至0%)与缓解之间存在明显的相关性。11例患者中,2例患有慢性粒细胞白血病,3例患有急性粒单核细胞白血病,3例患有急性髓细胞白血病,另外3例患有其他恶性血液系统疾病。我们得出结论,多倍体是与罕见白血病病例和其他恶性疾病相关的一个特征。它往往是预后不良的一个迹象。

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