Diffuse large B-cell lymphoma: one or more entities? Present controversies and possible tools for its subclassification

被引:61
作者
Pileri, SA
Dirnhofer, S
Went, P
Ascani, S
Sabattini, E
Marafioti, T
Tzankov, A
Leoncini, L
Faliniu, B
Zinzani, PL
机构
[1] Univ Bologna, Sch Med, Inst Haematol & Clin Oncol L&A Seragnoli, Chair Pathol Anat,Lymphoma Unit, I-40138 Bologna, Italy
[2] Univ Basel Hosp, Inst Pathol, CH-4031 Basel, Switzerland
[3] Univ Innsbruck, Inst Pathol, A-6020 Innsbruck, Austria
[4] Univ Siena, Inst Pathol, I-53100 Siena, Italy
[5] Univ Perugia, Monteluce Hosp, Haematopathol Lab, Chair Haematol 2, I-06100 Perugia, Italy
关键词
diffuse large B-cell lymphoma; morphology; phenotype; cytogenetics; genotype; clinics; tissue microarray; gene expression profiling;
D O I
10.1046/j.1365-2559.2002.01538.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Diffuse large B-cell lymphoma (DLBCL) is the commonest type of lymphoid tumour world-wide. This category was included both in the REAL and WHO Classification aiming to lump together all malignant lymphomas characterized by the large size of the neoplastic cells, B-cell derivation, aggressive clinical presentation, and the need for highly effective chemotherapy regimens. These tumours are detected as primary or secondary forms both at the nodal and extranodal levels, in immunocompetent hosts as well as in patients with different types of immunosuppression. They display a significant variability in terms of cell morphology and clinical findings, which justifies the identification of variants and subtypes. Among the latter, the primary mediastinal one does actually correspond to a distinct clinicopathological entity. Immunophenotypic, tissue microarray and molecular studies underline the extreme heterogeneity of DLBCLs and suggest a subclassification of the tumour, based on the identification of different pathogenic pathways, which might have much greater relevance than pure morphology for precise prognostic previsions and adoption of ad hoc therapies. The more recent acquisitions on the pathobiology of DLBCLs are reviewed in the light of the authors' experience, aiming to contribute to the existing debate on the topic.
引用
收藏
页码:482 / 509
页数:28
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