Tubbs R R, Sheibani K
Department of Pathology, Cleveland Clinic Foundation, Ohio 44106.
Semin Diagn Pathol. 1984 Nov;1(4):272-84.
Malignant lymphomas have come to be recognized as neoplasms of the immune system. These lymphoproliferative disorders demonstrate surface and cytoplasmic antigenic phenotypes that reflect qualitative and quantitative alterations or aberrant expression of genetic material. Traditionally, cell suspension studies have been used for phenotypic analysis. Alternative immunohistologic methods can be used to profile immunophenotypes in situ. Most lymphoproliferative disorders can be readily classified as T or B cell malignancies, and criteria have been evolved to differentiate neoplastic from reactive/physiologic expansions of lymphoid clones. However, antigenic phenotypic expression does not always correspond to known immunophenotypes of subsets of T or B cells and probably reflects the complexity of neoplastic transformation. Currently, frozen tissue sections, preferably in combination with cell suspension analysis using cytocentrifuge preparations and/or flow cytometry, can provide information to phenotype lymphomas classified by the International Formulation or other nomenclature. Their continued utility depends on development of and adherence to strict quality assurance programs.
恶性淋巴瘤已被公认为是免疫系统的肿瘤。这些淋巴增殖性疾病表现出表面和细胞质抗原表型,反映了遗传物质的定性和定量改变或异常表达。传统上,细胞悬液研究一直用于表型分析。也可采用其他免疫组织学方法原位分析免疫表型。大多数淋巴增殖性疾病可很容易地分类为T或B细胞恶性肿瘤,并且已经制定了标准以区分肿瘤性与反应性/生理性淋巴细胞克隆扩增。然而,抗原表型表达并不总是与已知的T或B细胞亚群免疫表型相对应,可能反映了肿瘤转化的复杂性。目前,冷冻组织切片,最好结合使用细胞离心涂片制备法和/或流式细胞术进行细胞悬液分析,可为按照国际分类法或其他命名法分类的淋巴瘤提供表型信息。它们能否持续发挥作用取决于严格质量保证计划的制定和遵守情况。