Griesser H, Henry M, Boie C, Banerjee D
Department of Pathology, University of Toronto, Canada.
Hematol Pathol. 1994;8(4):121-34.
Primary large-cell anaplastic lymphomas (LCAL) presenting in the gastrointestinal tract are rare and sometimes difficult to distinguish from nonlymphoid tumors. Because recognition of these tumors as lymphoma has clinical and prognostic implications for the patient, the diagnostic contribution of genotyping by polymerase chain reaction (PCR) and of immunophenotyping was evaluated in 16 routinely processed samples of gastric and small-intestinal LCALs. Gene rearrangement analysis was done with primers for the immunoglobulin heavy (IgH) and T-cell receptor gamma(TCR gamma) chain. Nine of the 16 cases were assigned to T- or B-lymphoid lineage immunophenotypically. Twelve of the 16 samples had a predominant T- or B-cell clone by PCR. Combination of both methods resulted in lineage assignment of 14 cases (9 T-LCAL, 5 B-LCAL). Two LCAL samples were EBV positive by PCR, one also by immunophenotyping. High expression levels of p53 did not correlate with the presence of EBV or cell lineage. Thus, gene rearrangement studies on routinely processed biopsy specimens by PCR are practical and add to the diagnostic repertoire in cases of gastrointestinal large-cell tumors of immunophenotypically undefined lineage.
原发于胃肠道的大细胞间变性淋巴瘤(LCAL)较为罕见,有时难以与非淋巴瘤性肿瘤相鉴别。鉴于将这些肿瘤识别为淋巴瘤对患者具有临床及预后意义,我们对16例经常规处理的胃及小肠LCAL样本进行了聚合酶链反应(PCR)基因分型及免疫表型分析,以评估其诊断价值。采用免疫球蛋白重链(IgH)和T细胞受体γ链(TCRγ)引物进行基因重排分析。16例病例中,9例经免疫表型分析确定为T或B淋巴细胞系。16个样本中有12个通过PCR检测显示主要为T或B细胞克隆。两种方法结合可对14例病例进行细胞系别判定(9例T-LCAL,5例B-LCAL)。2例LCAL样本经PCR检测显示EBV阳性,其中1例同时经免疫表型分析也为阳性。p53的高表达水平与EBV的存在或细胞系别无关。因此,通过PCR对常规处理的活检标本进行基因重排研究切实可行,可为免疫表型未明确的胃肠道大细胞肿瘤的诊断增添手段。