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霍奇金淋巴瘤、淋巴瘤样丘疹病及皮肤T细胞淋巴瘤源自一个共同的T细胞克隆。

Hodgkin's disease, lymphomatoid papulosis, and cutaneous T-cell lymphoma derived from a common T-cell clone.

作者信息

Davis T H, Morton C C, Miller-Cassman R, Balk S P, Kadin M E

机构信息

Department of Medicine, Beth Israel Hospital, Boston, MA 02215.

出版信息

N Engl J Med. 1992 Apr 23;326(17):1115-22. doi: 10.1056/NEJM199204233261704.

Abstract

BACKGROUND

Lymphomatoid papulosis is a benign cutaneous eruption that in 10 to 20 percent of patients is associated with the development of lymphoma. The atypical cells of lymphomatoid papulosis histologically resemble the malignant cells of cutaneous T-cell lymphoma or the Reed-Sternberg cells of Hodgkin's disease. We studied a patient in whom lymphomatoid papulosis developed in 1971, Hodgkin's disease in 1975, and cutaneous T-cell lymphoma in 1985, to determine whether these diseases are clonally related.

METHODS

The T-cell-receptor alpha-chain gene was cloned and sequenced from a cell line derived from the advanced-stage cutaneous T-cell lymphoma, and the polymerase chain reaction was used to search for this rearrangement of the alpha-chain gene in tissues obtained earlier that were affected by Hodgkin's disease or lymphomatoid papulosis.

RESULTS

The tumor-specific rearrangement of the alpha-chain gene was detected in the patient's earlier tissues affected by lymphomatoid papulosis and Hodgkin's disease, but not in control tissue, including uninvolved tissues from the staging laparotomy for Hodgkin's disease. Cytogenetic studies revealed a translocation, t(8;9)(p22;p24), in cutaneous T-cell lymphoma lines and in a dermatopathic lymph node removed two years before the clinical onset of the cutaneous T-cell lymphoma. Immunohistochemical findings were consistent with an activated T-cell phenotype for the atypical cells of lymphomatoid papulosis, the Reed-Sternberg cells of Hodgkin's disease, and the malignant cells of the T-cell lymphoma.

CONCLUSIONS

Lymphomatoid papulosis, Hodgkin's disease, and cutaneous T-cell lymphoma can be derived from a single T-cell clone. A t(8;9) genetic translocation may be involved in the pathogenesis of lymphomatoid papulosis or its progression to malignant disease.

摘要

背景

淋巴瘤样丘疹病是一种良性皮肤疹,10%至20%的患者会发展为淋巴瘤。淋巴瘤样丘疹病的非典型细胞在组织学上类似于皮肤T细胞淋巴瘤的恶性细胞或霍奇金病的里德-斯腾伯格细胞。我们研究了一名患者,该患者于1971年患淋巴瘤样丘疹病,1975年患霍奇金病,1985年患皮肤T细胞淋巴瘤,以确定这些疾病是否存在克隆相关性。

方法

从晚期皮肤T细胞淋巴瘤衍生的细胞系中克隆并测序T细胞受体α链基因,并使用聚合酶链反应在早期获得的受霍奇金病或淋巴瘤样丘疹病影响的组织中寻找α链基因的这种重排。

结果

在患者早期受淋巴瘤样丘疹病和霍奇金病影响的组织中检测到α链基因的肿瘤特异性重排,但在对照组织中未检测到,包括霍奇金病分期剖腹探查术中未受累的组织。细胞遗传学研究显示,在皮肤T细胞淋巴瘤细胞系以及皮肤T细胞淋巴瘤临床发病前两年切除的皮肤性淋巴结中存在易位t(8;9)(p22;p24)。免疫组织化学结果与淋巴瘤样丘疹病的非典型细胞、霍奇金病的里德-斯腾伯格细胞以及T细胞淋巴瘤的恶性细胞的活化T细胞表型一致。

结论

淋巴瘤样丘疹病、霍奇金病和皮肤T细胞淋巴瘤可能源自单个T细胞克隆。t(8;9)基因易位可能参与淋巴瘤样丘疹病的发病机制或其向恶性疾病的进展。

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