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89例扁桃体原发性非霍奇金淋巴瘤患者的临床特征

[Clinical features of 89 patients with primary non-Hodgkin's lymphoma of the tonsil].

作者信息

Qin Yan, Shi Yuan-Kai, He Xiao-Hui, Yang Jian-Liang, Yang Sheng, Yu Yan-Xia, Li Bo, Wang Qi-Lu, Zhou Li-Qiang, Sun Yan

机构信息

Department of Medical Oncology, Cancer Hospital/Cancer Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, P. R. China.

出版信息

Ai Zheng. 2006 Apr;25(4):481-5.

Abstract

BACKGROUND & OBJECTIVE: Head and neck lymphoma develops predominantly in the tonsil. This study was to investigate the clinical features of primary non-Hodgkin's lymphoma (NHL) of the tonsil, and to explore possible ways to improve the prognosis and quality of life of the patients after treatment.

METHODS

Clinical data of 89 naive patients with NHL of the tonsil, treated from May 1990 to Jan. 2003, were retrospectively reviewed. All patients were confirmed pathologically and classified according to revised European-American Lymphoid Neoplasms and World Health Organization Classification, and staged according to the Ann Arbor classification. Stage I-II patients received radiochemotherapy-predominant treatment, whereas stage III-IV patients received chemotherapy-predominant treatment.

RESULTS

Of the 89 cases, 60 (67%) were diffuse large B-cell subtype, 11 (12%) were peripheral T-cell subtype, 5 (6%) were indolent lymphoma, 1 was anaplastic large T-cell lymphoma, and 1 was T lymphoblastic lymphoma; 81 (91%) were stage I-II disease. Of the 89 patients, 58 (72%) received radiochemotherapy, 19 (21%) received radiotherapy alone, 3 received chemotherapy alone, and 1 received radiochemotherapy combined with rituximab. The 5-year overall survival rate was 80%, that of stage I-II patients was 84%. Cox regression multivariate analysis showed that the survival rate was correlated to the value of international prognostic index (IPI), and whether the patient had primary refractory or relapsed disease, but was not correlated to sex, age, pathologic subtype, B symptoms, and bulky disease.

CONCLUSIONS

Most patients with NHL of the tonsil are at early stages, with good prognosis. Diffuse large B-cell lymphoma is the most common pathologic subtype. Primary refractory, relapse, and IPI>1 are independent prognostic factors.

摘要

背景与目的

头颈部淋巴瘤主要发生于扁桃体。本研究旨在探讨扁桃体原发性非霍奇金淋巴瘤(NHL)的临床特征,并探索改善患者治疗后预后及生活质量的可能方法。

方法

回顾性分析1990年5月至2003年1月间收治的89例初治扁桃体NHL患者的临床资料。所有患者均经病理确诊,并根据欧美淋巴瘤修订分类及世界卫生组织分类进行分型,按Ann Arbor分期标准进行分期。Ⅰ-Ⅱ期患者以放化疗为主,Ⅲ-Ⅳ期患者以化疗为主。

结果

89例患者中,弥漫大B细胞亚型60例(67%),外周T细胞亚型11例(12%),惰性淋巴瘤5例(6%),间变性大T细胞淋巴瘤1例,T淋巴母细胞淋巴瘤1例;Ⅰ-Ⅱ期81例(91%)。89例患者中,58例(72%)接受放化疗,19例(21%)单纯接受放疗,3例单纯接受化疗,1例接受放化疗联合利妥昔单抗治疗。5年总生存率为80%,Ⅰ-Ⅱ期患者为84%。Cox回归多因素分析显示,生存率与国际预后指数(IPI)值及患者是否为原发性难治或复发性疾病相关,而与性别、年龄、病理亚型、B症状及大包块病无关。

结论

大多数扁桃体NHL患者处于早期,预后良好。弥漫大B细胞淋巴瘤是最常见的病理亚型。原发性难治、复发及IPI>1是独立的预后因素。

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