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真性红细胞增多症转化为急性非淋巴细胞白血病并伴有t(1;3)(p36;q21)核型。

Transformation of polycythemia vera to acute nonlymphocytic leukemia accompanied by t(1;3)(p36;q21) karyotype.

作者信息

Najfeld V, Coyle T, Berk P D

机构信息

Polly Annenberg Levee Hematology Center, Mount Sinai Medical Center, New York, NY 10029.

出版信息

Cancer Genet Cytogenet. 1988 Jul 15;33(2):193-200. doi: 10.1016/0165-4608(88)90029-5.

Abstract

The case of a patient with a history of polycythemia vera and 46,XX karyotype who transformed into acute nonlymphocytic leukemia with 46,XX,t(1;3)(p36;q21) rearrangement is reported. Significant percentages of the circulating blasts in the peripheral blood were positive on immunocytochemical stains for megakaryocyte markers, anti-Factor VIII, and antiglycoprotein IIb/IIIa. On the basis of our studies and published reports, trilineage hematopoietic abnormalities and a poor response to therapy may represent typical features of patients with t(1;3).

摘要

报告了一例真性红细胞增多症病史且核型为46,XX的患者,其转变为急性非淋巴细胞白血病,伴有46,XX,t(1;3)(p36;q21)重排。外周血中循环原始细胞的显著比例在免疫细胞化学染色中对巨核细胞标志物、抗凝血因子VIII和抗糖蛋白IIb/IIIa呈阳性。根据我们的研究和已发表的报告,三系造血异常和对治疗反应不佳可能是t(1;3)患者的典型特征。

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