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B细胞表型原发性胃淋巴瘤的临床病理研究,特别关注日本人群中的黏膜相关淋巴组织低度B细胞淋巴瘤。

Clinicopathologic study of primary gastric lymphoma of B cell phenotype with special reference to low-grade B cell lymphoma of mucosa-associated lymphoid tissue among the Japanese.

作者信息

Akaza K, Motoori T, Nakamura S, Koshikawa T, Kitoh K, Futamura N, Nakamura T, Kojima M, Kuroda M, Kasahara M

机构信息

Department of Pathology, Fujita Health University School of Medicine, Aichi, Japan.

出版信息

Pathol Int. 1995 Nov;45(11):832-45. doi: 10.1111/j.1440-1827.1995.tb03403.x.

Abstract

Resection specimens from 83 patients with primary gastric lymphoma (PGL) of B cell phenotype at stage IE and at stage IIE according to the Ann Arbor classification were investigated. Histologically, these lymphomas could be divided into four types: Type I lesions (n = 24) were entirely made up of MALT lymphoma; Type II lesions (n = 13) were predominantly MALT lymphoma containing one to a few foci of high-grade B cell lymphoma; Type III lesions (n = 22) consisted largely of high-grade lymphoma with small areas of low-grade MALT lymphoma; and Type IV lesions (n = 24) were pure high-grade B cell lymphoma, mostly of the large cell type. All patients had undergone primary gastric resection, and 14 received additional chemotherapy (n = 12), or both chemotherapy and radiotherapy (n = 2). The survival probability was significantly higher for Types I and II lymphomas than for Types III and IV tumors (P < 0.05 by the generalized Wilcoxon test). According to The General Rules for the Gastric Cancer Study by the Japanese Research Society for Gastric Cancer, the stage of disease showed a clear distinction between each of them (P < 0.01 by the generalized Wilcoxon test). This staging method seemed to serve well as a prognostic indicator. The histological typing of the PGL of the present series also seemed to correlate with the gross appearance, pathologic stage and prognosis. Furthermore, the expression of cyclin D1, bcl-2 and p53 protein, and PCNA was immunohistochemically investigated in 42 cases of the present series. Most of the low-grade PGL (Types I and II) had less than 60% PCNA-positive cells, whereas the high-grade PGL (Types III and IV) had more than 60% positive cells. In a study for cyclin D1 protein, no cases showed the nuclear staining pattern characteristic for mantle cell lymphoma, and the cytoplasmic staining frequently observed in the node-based large B cell lymphoma was seldom identified in the PGL. This discrepancy might suggest a lineage difference among the morphologically similar, but site-different, lymphomas. On the other hand, bcl-2 protein overexpression was almost equal in frequency between the gastric and node-based high-grade B cell lymphomas. This is in contrast to the reports from Western countries, in which the majority of high-grade gastric tumors were bcl-2 negative.

摘要

对83例根据Ann Arbor分期为IE期和IIE期的B细胞表型原发性胃淋巴瘤(PGL)患者的切除标本进行了研究。组织学上,这些淋巴瘤可分为四种类型:I型病变(n = 24)完全由黏膜相关淋巴组织淋巴瘤(MALT淋巴瘤)组成;II型病变(n = 13)主要是MALT淋巴瘤,含有1至数个高级别B细胞淋巴瘤灶;III型病变(n = 22)主要由高级别淋巴瘤组成,伴有小面积的低级别MALT淋巴瘤;IV型病变(n = 24)为纯高级别B细胞淋巴瘤,大多为大细胞型。所有患者均接受了原发性胃切除术,14例接受了额外化疗(n = 12),或化疗及放疗(n = 2)。I型和II型淋巴瘤的生存概率显著高于III型和IV型肿瘤(广义Wilcoxon检验,P < 0.05)。根据日本胃癌研究学会的《胃癌研究总则》,疾病分期在它们之间有明显差异(广义Wilcoxon检验,P < 0.01)。这种分期方法似乎是一个很好的预后指标。本系列PGL的组织学类型似乎也与大体外观、病理分期及预后相关。此外,对本系列中的42例进行了免疫组织化学研究,检测细胞周期蛋白D1、bcl-2和p53蛋白以及增殖细胞核抗原(PCNA)的表达。大多数低级别PGL(I型和II型)PCNA阳性细胞少于60%,而高级别PGL(III型和IV型)阳性细胞多于60%。在一项关于细胞周期蛋白D1蛋白的研究中,没有病例显示套细胞淋巴瘤特有的核染色模式,且在基于淋巴结的大B细胞淋巴瘤中经常观察到的胞质染色在PGL中很少见到。这种差异可能表明形态学相似但部位不同的淋巴瘤之间存在谱系差异。另一方面,胃高级别B细胞淋巴瘤和基于淋巴结的高级别B细胞淋巴瘤中bcl-2蛋白过表达的频率几乎相等。这与西方国家的报道相反,在西方国家,大多数高级别胃肿瘤bcl-2为阴性。

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