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美国人类T细胞淋巴瘤病毒(HTLV)阳性白血病 - 淋巴瘤的细胞遗传学研究

Cytogenetic studies in human T-cell lymphoma virus (HTLV)-positive leukemia-lymphoma in the United States.

作者信息

Whang-Peng J, Bunn P A, Knutsen T, Kao-Shan C S, Broder S, Jaffe E S, Gelmann E, Blattner W, Lofters W, Young R C

出版信息

J Natl Cancer Inst. 1985 Feb;74(2):357-69.

PMID:2983135
Abstract

Cytogenetic studies were conducted on fresh and cultured cells from 11 patients with human T-cell leukemia virus-associated adult T-cell leukemia-lymphoma. Clones with abnormal karyotypes were detected in 9 of the 11 patients. Chromosome numbers were near-diploid in cells from all but 1 patient who also had a tetraploid clone. The chromosome abnormalities in these cells were extensive; numerous complex structural changes were seen in every chromosome pair. Structural abnormalities occurred most frequently in chromosome 6. The 6 patients with chromosome 6 deletions had breakpoints at bands q11, q13, q16q23, q21q23, q22q24, and q23q24. The characteristic clinical features of these 6 patients were aggressive course, short survival, poor response to chemotherapy, high white blood cell counts, hypercalcemia, and bone lesions, whereas cytogenetically abnormal patients without chromosome 6q deletions tended to have a more indolent course. The precise role of the 6q deletion cannot be established with certainty from these data. However, this abnormality appears to occur with a greater than expected frequency in this large cell aggressive lymphoma, in association with hypercalcemia and lytic bone lesions.

摘要

对11例成人T细胞白血病-淋巴瘤患者的新鲜细胞和培养细胞进行了细胞遗传学研究。11例患者中有9例检测到核型异常的克隆。除1例患者有四倍体克隆外,其余患者细胞的染色体数目接近二倍体。这些细胞中的染色体异常广泛;在每对染色体中都观察到许多复杂的结构变化。结构异常最常出现在6号染色体上。6例6号染色体缺失的患者,断点位于q11、q13、q16q23、q21q23、q22q24和q23q24带。这6例患者的特征性临床特点为病程侵袭性、生存期短、对化疗反应差、白细胞计数高、高钙血症和骨病变,而细胞遗传学异常但无6q缺失的患者病程往往较为惰性。根据这些数据尚不能确定6q缺失的确切作用。然而,在这种大细胞侵袭性淋巴瘤中,这种异常出现的频率似乎高于预期,且与高钙血症和溶骨性骨病变有关。

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