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外周T细胞起源的成人T细胞淋巴瘤中的复发性染色体异常。

Recurrent chromosome abnormalities in adult T-cell lymphomas of peripheral T-cell origin.

作者信息

Fujita K, Fukuhara S, Nasu K, Yamabe H, Tomono N, Inamoto Y, Shimazaki C, Ohno H, Doi S, Kamesaki H

出版信息

Int J Cancer. 1986 Apr 15;37(4):517-24. doi: 10.1002/ijc.2910370408.

Abstract

Cytogenetic studies were performed on 11 Japanese patients with adult T-cell lymphoma of peripheral T-cell origin. All patients had a histologic diagnosis of diffuse lymphoma, and were treated with intensive combination chemotherapy; their median survival was 6 months. Lymphomas were categorized on the basis of the classification proposed by the Lymphoma Study Group of Japan: 5 patients had the features of pleomorphic lymphoma; 3, mixed lymphoma; 2, large-cell lymphoma; and 1, medium-sized-cell lymphoma. The modal chromosome number of abnormal cells was near-diploid in 7, and hypotetraploid in 4 including 3 patients with pleomorphic lymphoma. Abnormalities of the clonal chromosomes were observed in all 11 patients. A translocation of the short arm of 19 at band 19p13 was found in 2 patients with pleomorphic lymphoma and in one patient each with mixed lymphoma and medium-sized-cell lymphoma. A translocation of the short arm of 14, with a break at band 14p12, occurred in 4 patients with pleomorphic lymphoma. In one patient each with mixed lymphoma and large-cell lymphoma, an extra chromosome 3 was found. The numerical change was unique because their lymphomas were further categorized as "angioimmunoblastic lymphadenopathy with dysproteinemia" and "large-cell immunoblastic lymphoma", respectively. Our findings suggest that characteristic chromosome abnormalities occur in adult T-cell lymphoma, and dividing cells in the tetraploid range tend to be predominant in pleomorphic lymphoma.

摘要

对11例外周T细胞来源的日本成人T细胞淋巴瘤患者进行了细胞遗传学研究。所有患者均经组织学诊断为弥漫性淋巴瘤,并接受了强化联合化疗;他们的中位生存期为6个月。淋巴瘤根据日本淋巴瘤研究组提出的分类进行归类:5例具有多形性淋巴瘤特征;3例为混合性淋巴瘤;2例为大细胞淋巴瘤;1例为中细胞淋巴瘤。异常细胞的众数染色体数在7例中接近二倍体,4例为亚四倍体,其中3例为多形性淋巴瘤患者。11例患者均观察到克隆染色体异常。在2例多形性淋巴瘤患者、1例混合性淋巴瘤患者和1例中细胞淋巴瘤患者中发现了19号染色体短臂19p13处的易位。14号染色体短臂在14p12处断裂的易位发生在4例多形性淋巴瘤患者中。在1例混合性淋巴瘤患者和1例大细胞淋巴瘤患者中分别发现了一条额外的3号染色体。这种数量变化是独特的,因为他们的淋巴瘤分别被进一步归类为“伴有蛋白异常血症的血管免疫母细胞性淋巴结病”和“大细胞免疫母细胞性淋巴瘤”。我们的研究结果表明,成人T细胞淋巴瘤中存在特征性的染色体异常,并且在多形性淋巴瘤中四倍体范围内的分裂细胞往往占主导地位。

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