Clinicopathologic, enzyme and histochemical studies of centrocytic (mantle cell) lymphoma: comparison with other types of low-grade B cell lymphoma based on the updated Kiel classification.

M Takeshita, Y Masuda, Y Sumiyoshi, K Ohshima, M Kikuchi, N Kimura, T Okamura, J Nishimura, M Kozuru
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引用次数: 10

Abstract

Lymph nodes from 21 cases of malignant lymphoma of a centrocytic (mantle cell) type, (ML, cc (mc)) were examined. All the cases had monoclonal surface immunoglobulin (sig) M and/or D, but were negative for CD10 (CALLA), and CD11c (LeuM5). Lymphoma cells with CD25 (anti-Tac)+, CD5 (Leu1)+, and alkaline phosphatase (ALPase)- in eight cases showed bone marrow involvement (10-66% of the nucleated cells; mean 32 +/- 18%) but with no leukemic changes. These eight cases had a similar phenotype and were distributed by the lymphoma cells to the examined B-chronic lymphocytic leukemia. Seven cases showed an infiltration of CD25-, CD5+, and ALPase- lymphoma cells, in which only two cases showed focal bone marrow involvement. There was a close relationship between CD25 expression and bone marrow invasion by the lymphoma cells in ML, cc (mc). Three of the six CD25- and CD5- cases presented zonal proliferation of ALPase+ lymphoma cells with round nuclei and a high anti-proliferating cell nuclear antigen/cyclin (PCNA/c) rate in the mantle zone and paracortex, accompanied by a prominent interdigitating dendritic and histiocytic cell reaction. Examined CD25-, CD5- and ALPase+ lymphoma showed a neoplastic counterpart of so-called marginal zone lymphocytes, which was different from other cases of ML, cc (mc). Lymphoma cells in ML, cc (mc), except for those of the so-called marginal zone lymphoma, might be derived from slgM+, D+/-, CD25+/-, CD5+/-, ALPase-, CD10- and CD11c- lymphocytes present in the mantle zone and primary lymph follicles.(ABSTRACT TRUNCATED AT 250 WORDS)

中心细胞(套细胞)淋巴瘤的临床病理、酶和组织化学研究:基于更新的Kiel分类与其他类型低级别B细胞淋巴瘤的比较
本文对21例中心细胞(套细胞)型恶性淋巴瘤(ML, cc (mc))的淋巴结进行了检查。所有病例均有单克隆表面免疫球蛋白(sig) M和/或D,但CD10 (CALLA)和CD11c (LeuM5)阴性。8例有CD25(抗tac)+、CD5 (Leu1)+和碱性磷酸酶(ALPase)-的淋巴瘤细胞累及骨髓(10-66%的有核细胞;平均32±18%),但无白血病改变。这8例具有相似的表型,并由淋巴瘤细胞分布到所检查的b -慢性淋巴细胞白血病。7例显示CD25-、CD5+和ALPase-淋巴瘤细胞浸润,其中只有2例显示局灶性骨髓受累。在ML、cc (mc)中,CD25表达与淋巴瘤细胞侵袭骨髓密切相关。在6例CD25-和CD5-病例中,有3例出现了ALPase+淋巴瘤细胞的带状增殖,其核呈圆形,并且在套区和副皮层具有较高的抗增殖细胞核抗原/细胞周期蛋白(PCNA/c)率,并伴有明显的交叉树突状细胞和组织细胞反应。CD25-、CD5-和ALPase+淋巴瘤与其他ML、cc (mc)不同,均可见所谓的边缘区淋巴细胞的肿瘤对应物。除所谓的边缘区淋巴瘤外,ML、cc (mc)的淋巴瘤细胞可能来源于套区和原发淋巴滤泡中的slgM+、D+/-、CD25+/-、CD5+/-、ALPase-、CD10-和CD11c-淋巴细胞。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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