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p27Kip1 Immunostaining for the Differential Diagnosis of Small B-Cell Neoplasms in Trephine Bone Marrow Biopsies

机译:p27Kip1免疫染色法用于在Trephine骨髓活检中鉴别小B细胞肿瘤

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The distinction between mantle cell lymphoma (MCL) and other small B-cell non-Hodgkin lymphomas (NHL) is important because MCL has a more aggressive clinical course. In bone marrow (BM) biopsy specimens, this distinction can be particularly difficult. Although cyclin D1 immunostaining and molecular detection of the t(11;14) translocation are highly specific markers for MCL, they fail to detect a proportion of cases. We have recently described that MCL typically lacks detectable expression of the cyclin-dependent kinase inhibitor p27kip1 protein by immunostaining, which is expressed at high levels in most small B-cell NHL inversely correlated to the proliferation rate. We therefore examined whether p27kip1 immunostaining could be a useful adjunct for the differential diagnosis of small B-cell NHL infiltrates in the BM. Trephine BM biopsy specimens of 96 patients, including well-characterized MCL (19 cases), B-cell chronic lymphocytic leukemia (27 cases), follicular lymphoma (18 cases), hairy cell leukemia (22 cases), and marginal zone lymphoma (10 cases) as well as 10 reactive BM, including five with benign lymphoid aggregates were investigated. In addition, the presence of a t(11;14) translocation involving the major translocation cluster was studied by PCR in all MCL. All cases of B-cell chronic lymphocytic leukemia, follicular lymphoma, and marginal zone lymphoma revealed a strong p27kip1 nuclear staining in the majority of neoplastic cells. Fourteen (78%) cases of MCL were p27kip1-negative in the tumor cells, whereas four cases revealed a weak nuclear positivity. Seventeen (77%) cases of hairy cell leukemia were also either completely negative for p27kip1 or showed a faint positive staining in a minority of the neoplastic cells. Nine of 19 cases (47%) of MCL showed a bcl1 rearrangement involving the major translocation cluster region. These findings demonstrate that p27kip1 immunostaining is a valuable additional marker for the differential diagnosis of small B-cell NHL infiltrates in BM biopsies. The reduction or lack of p27kip1 protein expression in MCL, as well as in hairy cell leukemia, might be an important event in the pathogenesis of these disorders.
机译:外套细胞淋巴瘤(MCL)与其他小B细胞非霍奇金淋巴瘤(NHL)之间的区别很重要,因为MCL具有更积极的临床过程。在骨髓活检标本中,这种区分可能特别困难。尽管细胞周期蛋白D1免疫染色和t(11; 14)易位的分子检测是MCL的高度特异性标记,但它们无法检测到一定比例的病例。我们最近描述了MCL通常缺乏通过免疫染色检测到的细胞周期蛋白依赖性激酶抑制剂p27kip1蛋白的表达,这种表达在大多数与增殖速率成反比的B细胞NHL中以高水平表达。因此,我们检查了p27kip1免疫染色是否可能是鉴别BM中小B细胞NHL浸润的有用辅助方法。 Trephine BM活检标本96例,包括特征明确的MCL(19例),B细胞慢性淋巴细胞性白血病(27例),滤泡性淋巴瘤(18例),毛细胞白血病(22例)和边缘区淋巴瘤(10例)病例)以及10例反应性BM,包括5例良性淋巴样聚集物进行了调查。此外,通过PCR在所有MCL中研究了涉及主要易位簇的t(11; 14)易位。所有B细胞慢性淋巴细胞性白血病,滤泡性淋巴瘤和边缘区淋巴瘤的病例在大多数肿瘤细胞中均显示出强烈的p27kip1核染色。肿瘤细胞中14例(78%)MCL呈p27kip1阴性,而4例显示核阳性较弱。 17例(77%)毛细胞白血病患者的p27kip1也完全阴性或在少数肿瘤细胞中呈淡淡阳性染色。 19例MCL中有9例(47%)显示bcl1重排,涉及主要易位簇区域。这些发现表明,p27kip1免疫染色是用于BM活检中小B细胞NHL浸润的鉴别诊断的有价值的附加标记。 MCL以及毛细胞白血病中p27kip1蛋白表达的减少或缺乏可能是这些疾病发病机理中的重要事件。

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