l26阳性、cd15阴性的霍奇金病和反应性t细胞含量高的大b细胞淋巴瘤的鉴别诊断:形态学和免疫组织化学研究

D T Nguyen, L W Diamond, M L Hansmann, R Fischer
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引用次数: 0

摘要

具有明显优势的反应性T细胞的b细胞非霍奇金淋巴瘤,即所谓的富T细胞b细胞淋巴瘤(TCRBCLs),在形态学上可能与霍奇金病(HD)混淆。本文对10例l26阳性、cd15阴性的HD和10例TCRBCL进行比较,以建立石蜡切片的鉴别特征;4例HD的形态学特征为结节性淋巴细胞显性(LP)型。10例HD中有9例含有少于20个核分裂/20个高倍视野(hpf),只有1例累及囊包膜。相比之下,10例TCRBCL中有9例有丝分裂大于20 /20 hpf, 7例有淋巴结周围浸润。HDLP很容易与TCRBCL区分,通过扩大的树突网络勾勒出L和H结节和高含量的cd57阳性淋巴细胞。其余6例非lp L26阳性HD的免疫染色模式相对独特,在Reed-Sternberg细胞和变体中缺乏CD45, L26和Ki-B5的反应性不一致。只有3例TCRBCL具有相似的CD45和L26/Ki-B5免疫染色模式,这些可以通过明显的细胞质轻链限制来区分。这些结果表明,当只有固定材料可用时,评估有丝分裂计数、包膜受损伤和Ki-M4p、CD57、L26/Ki-B5和CD45的免疫组织化学染色模式有助于区分TCRBCL和L26阳性HD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential diagnosis of L26-positive, CD15-negative Hodgkin's disease and large B-cell lymphoma with a high content of reactive T-cells: a morphologic and immunohistochemical study.

B-cell non-Hodgkin's lymphomas with a marked preponderance of reactive T cells, so-called T-cell rich B-cell lymphomas (TCRBCLs), can be morphologically confused with Hodgkin's disease (HD). To establish helpful distinguishing features in paraffin sections, 10 cases of L26-positive, CD15-negative HD and 10 cases of TCRBCL were compared; 4 cases of HD had morphologic features of the nodular lymphocyte predominant (LP) type. Nine of 10 cases of HD contained fewer than 20 mitoses/20 high power fields (hpf) and only 1 had pericapsular involvement. In contrast, 9 of 10 TCRBCL had greater than 20 mitoses/20 hpf and 7 had perinodal infiltration. HDLP was easily distinguished from TCRBCL by the expanded dendritic meshworks outlining the L & H nodules and the high content of CD57-positive lymphocytes. The remaining 6 cases of non-LP L26-positive HD had a relatively distinctive immunostaining pattern, with absence of CD45 and discordant reactivity for L26 and Ki-B5 in Reed-Sternberg cells and variants. Only 3 cases of TCRBCL had a similar CD45 and L26/Ki-B5 immunostaining pattern, and these could be distinguished by demonstrable cytoplasmic light-chain restriction. These results show that evaluation of the mitotic count, pericapsular involvement, and immunohistochemical staining patterns for Ki-M4p, CD57, L26/Ki-B5, and CD45 can help to discriminate TCRBCL from L26-positive HD when only fixed material is available.

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