Department of Pathology, Hematopathology Section and Lymph Node Registry, Christian-Albrechts-University Kiel, University Hospital Schleswig-Holstein, Kiel, Germany.
Haematologica. 2011 Feb;96(2):262-8. doi: 10.3324/haematol.2010.030809. Epub 2010 Oct 22.
Background Primary mediastinal large B-cell lymphoma is a rare lymphoma accounting for no more than 3% of all B-cell lymphomas in children and adolescents. However, patients in this young age group with this lymphoma have the shortest event-free survival of patients with any B-cell lymphoma under current standard chemotherapy protocols. Lymphomas with features intermediate between primary mediastinal large B-cell lymphoma and classical Hodgkin's lymphoma (mediastinal gray zone lymphomas) have been acknowledged in the latest World Health Organization classification. Recent studies suggest that mediastinal gray zone lymphomas have an aggressive clinical course whereas patients, at least adult ones, with primary mediastinal large B-cell lymphoma might respond very well to chemotherapy in combination with anti-CD20 antibody.
We aimed to evaluate whether biological differences or so far unrecognized admixed mediastinal gray zone lymphomas might explain the relatively poor outcome of pediatric patients with apparent primary mediastinal large B-cell lymphoma. We, therefore, performed a retrospective histopathological, immunohistochemical and interphase cytogenetic analysis of 52 pediatric lymphomas.
The childhood primary mediastinal large B-cell lymphomas (n=44) showed a similar pattern of histology, immunophenotype and gains at 9p (59%) and 2p (41%) as adult cases, as determined from published data. We identified only four so far unrecognized cases of mediastinal gray zone lymphoma among 52 lymphomas registered in previous trials. Conclusions Mediastinal gray zone lymphoma is very rare in children and adolescents. It does, therefore, seem unlikely that these lymphomas account for the unsatisfactory clinical results with current therapy protocols in pediatric patients. These data have major implications for the design of future treatment protocols for mediastinal lymphomas in children and adolescents.
原发性纵隔大 B 细胞淋巴瘤是一种罕见的淋巴瘤,在儿童和青少年的所有 B 细胞淋巴瘤中所占比例不超过 3%。然而,在当前标准化疗方案下,该年龄段的此类患者无事件生存时间是所有 B 细胞淋巴瘤患者中最短的。在最新的世界卫生组织分类中,已经承认了介于原发性纵隔大 B 细胞淋巴瘤和经典霍奇金淋巴瘤之间的特征的淋巴瘤(纵隔灰色区淋巴瘤)。最近的研究表明,纵隔灰色区淋巴瘤具有侵袭性的临床病程,而至少成年患者的原发性纵隔大 B 细胞淋巴瘤可能对联合抗 CD20 抗体的化疗反应非常好。
我们旨在评估是否存在生物学差异或迄今为止未被识别的混合纵隔灰色区淋巴瘤可能解释了明显原发性纵隔大 B 细胞淋巴瘤的儿科患者预后相对较差的原因。因此,我们对 52 例儿科淋巴瘤进行了回顾性组织病理学、免疫组织化学和间期细胞遗传学分析。
儿童原发性纵隔大 B 细胞淋巴瘤(n=44)表现出与成人病例相似的组织学、免疫表型和 9p(59%)和 2p(41%)增益模式,这是根据已发表的数据确定的。在以前的试验中注册的 52 例淋巴瘤中,我们仅发现了 4 例迄今为止未被识别的纵隔灰色区淋巴瘤。
纵隔灰色区淋巴瘤在儿童和青少年中非常罕见。因此,似乎不太可能这些淋巴瘤导致当前治疗方案在儿科患者中临床效果不理想。这些数据对儿童和青少年纵隔淋巴瘤未来治疗方案的设计具有重大意义。