Coupland S E, Krause L, Delecluse H J, Anagnostopoulos I, Foss H D, Hummel M, Bornfeld N, Lee W R, Stein H
Department of Pathology, Universitätsklinikum Benjamin Franklin, Freie Universität, Berlin, Germany.
Ophthalmology. 1998 Aug;105(8):1430-41. doi: 10.1016/S0161-6420(98)98024-1.
Lymphoproliferative lesions of the ocular adnexa were analyzed to examine (1) the suitability of the Revised European-American Lymphoma (REAL) classification for the subtyping of the lymphomas in these sites; (2) the predictive value of the REAL classification for the evolution of these tumors; and (3) the frequency and prognostic impact of tumor type, location, proliferation rate (Ki-67 index), p53, CD5 positivity and the presence of monoclonality within these tumors.
Retrospective review.
The clinical, histomorphologic, immunohistochemical, and molecular biologic (polymerase chain reaction [PCR]) features of lymphoid proliferations of the ocular adnexa were studied. STUDY MATERIALS: The ocular adnexal lymphoproliferative lesions were located as follows: orbit in 52 patients (46%), conjunctiva in 32 patients (29%), eyelid in 23 patients (21%), and caruncle in 5 patients (4%).
Reactive lymphoid hyperplasia was diagnosed in 12 cases and lymphoma in 99 cases; 1 case remained indeterminate. The five main subtypes of lymphoma according to the REAL classification were extranodal marginal-zone B-cell lymphoma (64%), follicle center lymphoma (10%), diffuse large cell B-cell lymphoma (9%), plasmacytoma (6%), and lymphoplasmocytic lymphoma (5%). Age, gender, and anatomic localization of the lymphomas did not have prognostic significance during a follow-up period of 6 months to 16.5 years (mean, 3.3 years). Extent of disease at time of presentation was the most important clinical prognostic factor: advanced disease correlated with increased risk ratios of having persistent disease at the final follow-up and with lymphoma-related death (P < 0.001). Histomorphologic features and immunohistochemical markers positively correlating with disseminated disease at presentation, stage at final follow-up, and occurrence of lymphoma-related death included cytologic atypia (P < 0.001), MIB-1 proliferation rate (P < 0.001), and tumor cell p53 positivity (P < 0.001). The MIB-1 proliferation rates greater than 20% in extranodal marginal-zone B-cell lymphoma corresponded to at least stage II lymphoma (P < 0.05).
The REAL classification is suitable for the subdivision of the ocular adnexal lymphomas. The MIB-1 proliferation rate and p53 positivity may aid the prediction of disease stage and disease progression, whereas PCR can support the diagnosis and reduce the number of histologically indeterminate lesions.
分析眼附属器的淋巴增生性病变,以检验:(1)修订的欧美淋巴瘤(REAL)分类对这些部位淋巴瘤亚型分类的适用性;(2)REAL分类对这些肿瘤演变的预测价值;(3)肿瘤类型、位置、增殖率(Ki-67指数)、p53、CD5阳性以及这些肿瘤内单克隆性的频率和预后影响。
回顾性研究。
研究眼附属器淋巴增生的临床、组织形态学、免疫组织化学和分子生物学(聚合酶链反应[PCR])特征。研究材料:眼附属器淋巴增生性病变的分布如下:眼眶52例(46%),结膜32例(29%),眼睑23例(21%),泪阜5例(4%)。
诊断为反应性淋巴增生12例,淋巴瘤99例;1例仍不能确诊。根据REAL分类,淋巴瘤的五种主要亚型为结外边缘区B细胞淋巴瘤(64%)、滤泡中心淋巴瘤(10%)、弥漫性大细胞B细胞淋巴瘤(9%)、浆细胞瘤(6%)和淋巴浆细胞淋巴瘤(5%)。在6个月至16.5年(平均3.3年)的随访期间,淋巴瘤患者的年龄、性别和解剖学定位均无预后意义。就诊时的疾病范围是最重要的临床预后因素:晚期疾病与最终随访时持续性疾病风险增加以及淋巴瘤相关死亡相关(P<0.001)。与就诊时播散性疾病、最终随访分期和淋巴瘤相关死亡相关的组织形态学特征和免疫组织化学标志物包括细胞异型性(P<0.001)、MIB-1增殖率(P<0.