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恶性淋巴瘤,小淋巴细胞型:84例临床病理研究及中间淋巴细胞淋巴瘤的推荐标准

Malignant lymphoma, small lymphocytic type: a clinicopathologic study of 84 cases with suggested criteria for intermediate lymphocytic lymphoma.

作者信息

Evans H L, Butler J J, Youness E L

出版信息

Cancer. 1978 Apr;41(4):1440-55. doi: 10.1002/1097-0142(197804)41:4<1440::aid-cncr2820410432>3.0.co;2-g.

Abstract

Clinical and histopathologic findings were reviewed in 84 cases of malignant lymphoma of the small (well differentiated) lymphocytic type. The slides were studied without clinical information, and the following morphologic features were evaluated: pattern of growth, number of large lymphocytes, mitotic rate, degree of capsular involvement, presence of plasma cells and/or plasmacytoid lymphocytes, and presence of residual germinal centers. Subsequently, clinical information was obtained. The minimum follow-up period on living patients was 5 years. The patients were divided into 3 clinical categories: 1) monoclonal gammopathy (MG)-11 cases, 2) chronic lymphocytic leukemia (CLL) without MG-56 cases, and 3) those without MG or CLL at the time of lymph node biopsy-17 cases. The criterion for CLL was an initial absolute lymphocyte count less than 4000/mm3. Four of the patients with MG also had CLL, and 6 of those in the third group later developed CLL, from 1 to 61 months after lymph node biopsy. Generalized lymphadenopathy was the usual presentation in all 3 groups, and bone marrow examination was positive in all but 1 of the 49 cases, representing all 3 groups, in which it was performed. Median survival for the 84 patients was 51 months. The only clinical parameters which showed a significant association with poorer survival were age above 60 and anemia (Hb. conc. less than 11.0). There was no significant relationship between morphologic characteristics and clinical categories other than the association of plasmacytoid cells with MG in 6 cases. A mitotic rate of 30 or more mitoses per 20 high power fields (HPF), found in 5 cases with at least 1 in each clinical category, showed a highly significant association with decreased survival (p = .01). Variations in mitotic rate between 0 and 29 mitoses per 20 HPF and other morphologic parameters did not show a significant relationship with prognosis. It was concluded that malignant lymphoma of the small lymphocytic type is a definite clinicopathologic entity which may or may not exhibit MG or CLL, and it is proposed that the term "intermediate lymphocytic lymphoma" be applied only to those cases showing histopathologic characteristics of small lymphocytic lymphoma and a mitotic rate of 30 or more mitoses per 20 HPF.

摘要

回顾了84例小(高分化)淋巴细胞型恶性淋巴瘤的临床和组织病理学表现。在不了解临床信息的情况下研究切片,并评估以下形态学特征:生长模式、大淋巴细胞数量、有丝分裂率、包膜受累程度、浆细胞和/或浆细胞样淋巴细胞的存在以及残留生发中心的存在。随后获取临床信息。存活患者的最短随访期为5年。患者分为3个临床类别:1)单克隆丙种球蛋白病(MG)-11例,2)无MG的慢性淋巴细胞白血病(CLL)-56例,3)淋巴结活检时无MG或CLL的患者-17例。CLL的标准是初始绝对淋巴细胞计数低于4000/mm³。11例MG患者中有4例也患有CLL,第三组中的6例在淋巴结活检后1至61个月后来发展为CLL。全身淋巴结肿大是所有3组的常见表现,49例(代表所有3组)中除1例外在进行骨髓检查时均呈阳性。84例患者的中位生存期为51个月。与较差生存率有显著关联的唯一临床参数是年龄大于60岁和贫血(血红蛋白浓度低于11.0)。除6例浆细胞样细胞与MG相关外,形态学特征与临床类别之间无显著关系。在每个临床类别中至少有1例的5例患者中,发现每20个高倍视野(HPF)有30个或更多有丝分裂,这与生存率降低高度相关(p = 0.01)。每20个HPF有丝分裂率在0至29个之间的变化以及其他形态学参数与预后无显著关系。结论是,小淋巴细胞型恶性淋巴瘤是一种明确的临床病理实体,可能表现或不表现MG或CLL,并建议术语“中间淋巴细胞淋巴瘤”仅适用于那些显示小淋巴细胞淋巴瘤组织病理学特征且每20个HPF有丝分裂率为30个或更多的病例。

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