Crist W M, Kelly D R, Ragab A H, Roper M, Dearth J C, Castleberry R P, Flint A
Cancer. 1981 Nov 1;48(9):2070-5. doi: 10.1002/1097-0142(19811101)48:9<2070::aid-cncr2820480925>3.0.co;2-u.
Tissues from 22 children with non-Hodgkin lymphoma (NHL) were studied pathologically and immunologically. Most children were noted to have marked (B- or T-cell) neoplasms and the Lukes-Collins classification was predictive of immunologic phenotype in cases where markers were present. Our series and a review of the literature demonstrates that most abdominal NHL are B-cell in origin and are often small noncleaved follicular center cell lymphoma (Burkitt type). Most mediastinal primary lesions are T-cell in origin and of convoluted cell morphology. A few neoplasms (often peripheral nodal) lack the characteristic surface immunoglobulin or erythrocyte rosetting properties of B- or T-cell lesions, respectively. Frequently marrow and central nervous system involvement are observed in T-cell lymphomas and are not in frequent in B cell neoplasms. Shared immunologic and clinical features between the B- or T-cell lymphomas and their leukemic counterparts support the concept that they often differ only in the stage of disease progression.
对22例非霍奇金淋巴瘤(NHL)患儿的组织进行了病理和免疫研究。多数患儿表现为显著的(B细胞或T细胞)肿瘤,在有标记物的病例中,Lukes-Collins分类可预测免疫表型。我们的系列研究及文献回顾表明,多数腹部NHL起源于B细胞,常为小无裂滤泡中心细胞淋巴瘤(伯基特型)。多数纵隔原发性病变起源于T细胞,具有卷曲细胞形态。少数肿瘤(常为外周淋巴结)分别缺乏B细胞或T细胞病变特征性的表面免疫球蛋白或红细胞花环形成特性。T细胞淋巴瘤常累及骨髓和中枢神经系统,而B细胞肿瘤则不常见。B细胞或T细胞淋巴瘤与其白血病对应物之间共有的免疫和临床特征支持这样的概念,即它们通常仅在疾病进展阶段有所不同。