Frater J L, Tsiftsakis E K, Hsi E D, Pettay J, Tubbs R R
Department of Clinical Pathology, Cleveland Clinic Foundation, Ohio 44195, USA.
Diagn Mol Pathol. 2001 Dec;10(4):214-22. doi: 10.1097/00019606-200112000-00002.
Increasingly, molecular biologic techniques have become important in the diagnosis of non-Hodgkin lymphomas. In the differential diagnosis of lymphoma(s) of small lymphocytes (LSL), reliable detection of t(11;14) or t(14;18) would confirm the diagnosis of mantle cell lymphoma (MCL) or follicle center lymphoma (FCL), respectively. A total of 87 LSL cases (27 MCL, 39 FCL, 17 small lymphocytic lymphoma [SLL], 3 marginal zone lymphomas, and 1 paraimmunoblastic variant of SLL) were diagnosed by a combination of light microscopy, immunohistochemistry, and flow cytometric immunophenotyping. Interphase fluorescence in situ hybridization (FISH) for t(11;14) and t( 14;18) using dual-fusion probes (Vysis, Downers Grove, IL) was performed on touch (n = 69) or gravity (n = 18) preparations from these cases. Of 27 MCL cases tested, 25 (93%) had demonstrable t(11;14), none had t(14;18), and 2 were negative for t(11;14) and t(14;18). Twenty-five of 39 (64%) FCL cases had t(14;18), none had t(11;14), and the remaining FCL cases (14 cases [35%]) had neither t(11;14) nor t(14;18). All 17 (100%) SLL cases had neither t(11;14) nor t(14;18). All 3 (100%) marginal zone lymphoma cases had neither t(11;14) nor t(14;18). The case of paraimmunoblastic variant of SLL had t(11;14) and was negative for t(14;18). No discrepant [i.e., positive for both t(11;14) and t(14;18)] or false-positive cases were noted. Interphase FISH using these commercially available probes is a useful adjunct to light microscopy, immunohistochemistry, and flow cytometric immunophenotyping in the diagnosis of LSL. FISH can be performed successfully on archival single-cell preparations (touch preparations or gravity preparations) when fresh tissue is unavailable. No discordant or false-positive cases were identified.
分子生物学技术在非霍奇金淋巴瘤的诊断中日益重要。在小淋巴细胞淋巴瘤(LSL)的鉴别诊断中,可靠检测t(11;14)或t(14;18)分别可确诊套细胞淋巴瘤(MCL)或滤泡中心淋巴瘤(FCL)。通过光学显微镜、免疫组织化学和流式细胞免疫表型分析相结合的方法,共诊断出87例LSL病例(27例MCL、39例FCL、17例小淋巴细胞淋巴瘤[SLL]、3例边缘区淋巴瘤和1例SLL的副免疫母细胞变异型)。使用双色融合探针(Vysis,伊利诺伊州唐纳德斯格罗夫)对这些病例的触片(n = 69)或自然沉降片(n = 18)进行t(11;14)和t(14;18)的间期荧光原位杂交(FISH)检测。在检测的27例MCL病例中,25例(93%)可检测到t(11;14),无t(14;18),2例t(11;14)和t(14;18)均为阴性。39例FCL病例中有25例(64%)有t(14;18),无t(11;14),其余FCL病例(14例[35%])既无t(11;14)也无t(14;18)。所有17例(100%)SLL病例既无t(11;14)也无t(14;18)。所有3例(100%)边缘区淋巴瘤病例既无t(11;14)也无t(14;18)。SLL的副免疫母细胞变异型病例有t(11;14),t(14;18)为阴性。未发现不一致(即t(11;14)和t(14;18)均为阳性)或假阳性病例。使用这些市售探针进行的间期FISH是LSL诊断中光学显微镜、免疫组织化学和流式细胞免疫表型分析的有用辅助手段。当无法获得新鲜组织时,可在存档的单细胞标本(触片或自然沉降片)上成功进行FISH检测。未发现不一致或假阳性病例。