Mollejo Manuela, Algara Patrocino, Mateo Marisol S, Menárguez Javier, Pascual Esperanza, Fresno Manuel F, Camacho Francisca I, Piris Miguel A
Lymphoma Group, Molecular Pathology Program, Centro Nacional de Investigaciones Oncológicas, Madrid, Spain.
Am J Surg Pathol. 2003 Jul;27(7):895-902. doi: 10.1097/00000478-200307000-00004.
Only a few series of splenic large B-cell lymphoma have been previously reported, including limited immunophenotypic studies and clinical data. Here we review the clinical data, morphology, and immunophenotype of series of 33 cases of large B-cell lymphoma presenting in the spleen. Three main groups of tumors are identified. Group A was characterized by macronodular tumors (20 cases), with predominantly stage I disease and a favorable clinical outcome. All cases were bcl6 positive. Group B was characterized by a micronodular pattern (nine cases), including a subset with T-cell-rich B-cell lymphoma features. Most of the patients in this group were diagnosed at advanced clinical stages and died of the disease. All cases were bcl6 positive. Group C was characterized by diffuse red pulp infiltration (four cases) and advanced clinical stages and showed an aggressive behavior. All but one case were bcl6 positive. The results of this series define a characteristic type of large B-cell lymphoma presenting in the spleen as a tumoral mass, associated with a relatively favorable clinical course. Additionally, they provide evidence that clinical presentation as a tumor confined to the spleen and the hilar lymph nodes is associated with lower aggressivity.
此前仅有少数关于脾大B细胞淋巴瘤的系列报道,包括有限的免疫表型研究和临床数据。在此,我们回顾了33例脾脏大B细胞淋巴瘤的临床数据、形态学及免疫表型。确定了三种主要的肿瘤类型。A组以大结节性肿瘤为特征(20例),主要为I期疾病,临床预后良好。所有病例bcl6均呈阳性。B组以小结节模式为特征(9例),包括一部分具有富于T细胞的B细胞淋巴瘤特征的病例。该组大多数患者在临床晚期被诊断,死于该疾病。所有病例bcl6均呈阳性。C组以弥漫性红髓浸润为特征(4例),处于临床晚期,表现出侵袭性。除1例病例外,所有病例bcl6均呈阳性。该系列结果确定了一种特征性的大B细胞淋巴瘤类型,其表现为脾脏肿瘤块,临床病程相对良好。此外,它们提供了证据表明,表现为局限于脾脏和肺门淋巴结的肿瘤与较低的侵袭性相关。