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与20号染色体长臂缺失相关的血液学表现

Hematologic manifestations associated with deletions of the long arm of chromosome 20.

作者信息

Davis M P, Dewald G W, Pierre R V, Hoagland H C

出版信息

Cancer Genet Cytogenet. 1984 May;12(1):63-71. doi: 10.1016/0165-4608(84)90009-8.

Abstract

We investigated 20 patients with hematologic disorders who had a clone of cells with a deletion of most of a chromosome #20 long arm (20q-) in the bone marrow. Three patients had polycythemia vera (PV), 6 had acute nonlymphocytic leukemia (ANLL), 8 had preleukemia (PL), and 3 had other myeloproliferative disorders. In our laboratory, a 20q- chromosome is found in 6% of patients with PV, 3% of patients with ANLL, and 1% of patients with PL. Among the 6 patients with ANLL and a 20q- abnormality, 3 had erythroleukemia. There were no apparent clinical differences among our patients with 20q- chromosomes compared with other patients with similar disorders who did not have a 20q- chromosome. The breakpoint of the 20q- anomaly, in each instance, was in band 20q11, but it occurred near the centromere at 20q1101 in 16 patients and at the distal part of this band at 20q1109 in 4 patients. Three of the 4 patients with a breakpoint at 20q1109 had PL.

摘要

我们研究了20例血液系统疾病患者,这些患者骨髓中存在一个细胞克隆,其20号染色体长臂大部分缺失(20q-)。3例患者患有真性红细胞增多症(PV),6例患有急性非淋巴细胞白血病(ANLL),8例患有白血病前期(PL),3例患有其他骨髓增殖性疾病。在我们实验室,PV患者中6%、ANLL患者中3%以及PL患者中1%可发现20q-染色体。在6例患有ANLL且存在20q-异常的患者中,3例患有红白血病。与其他患有类似疾病但无20q-染色体的患者相比,我们的20q-染色体患者之间没有明显的临床差异。在每个病例中,20q-异常的断点位于20q11带,但16例患者的断点在20q1101靠近着丝粒处,4例患者的断点在该带的远端20q1109处。4例断点在20q1109的患者中有3例患有PL。

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