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弥漫性大B细胞淋巴瘤的梭形细胞变体具有生发中心B细胞起源的基因型和表型标志物。

A spindle cell variant of diffuse large B-cell lymphoma possesses genotypic and phenotypic markers characteristic of a germinal center B-cell origin.

作者信息

Carbone Antonino, Gloghini Annunziata, Libra Massimo, Gasparotto Daniela, Navolanic Patrick M, Spina Michele, Tirelli Umberto

机构信息

Department of Pathology, Istituto Nazionale Tumori, Milano, Italy.

出版信息

Mod Pathol. 2006 Feb;19(2):299-306. doi: 10.1038/modpathol.3800540.

Abstract

Lymphoma with prominent spindle cell features, the so-called spindle cell lymphoma, is an unusual morphological variant of diffuse large B-cell lymphoma. Five new cases of spindle cell lymphoma have been analyzed by a multiparameter approach in order to clarify its clinical and biological features. All patients presented advanced stage disease with extranodal involvement. Vagina was the most common extranodal site. All patients received chemotherapy and are alive in complete remission. Morphologically, all five cases exhibited proliferation of spindle cells with a vaguely storiform pattern highly suggestive of spindle cell neoplasms of nonlymphoid origin. In contrast, the results of immunohistochemical analysis indicated that all five cases were hematolymphoid neoplasms of the B-cell lineage. These lymphomas consisted of a B-cell clonal population which exhibited somatic immunoglobulin and BCL-6 mutations as well as BCL-6 protein expression. The neoplastic spindle cells therefore closely resemble B cells residing in the germinal center. The absence of MUM1 expression in neoplastic spindle cells suggested that neoplastic spindle cells may be related to the early phases of intragerminal center maturation of B cells. The germinal center phenotype, with restricted expression of BCL-6, was associated with the presence of a primary extranodal origin, normal lactate dehydrogenase levels, and good response to treatment.

摘要

具有显著梭形细胞特征的淋巴瘤,即所谓的梭形细胞淋巴瘤,是弥漫性大B细胞淋巴瘤一种不常见的形态学变异型。为阐明其临床和生物学特征,采用多参数方法分析了5例新的梭形细胞淋巴瘤病例。所有患者均表现为晚期疾病并伴有结外受累。阴道是最常见的结外部位。所有患者均接受了化疗,目前存活且处于完全缓解状态。形态学上,所有5例病例均表现为梭形细胞增殖,呈模糊的席纹状模式,高度提示非淋巴源性梭形细胞瘤。相比之下,免疫组化分析结果表明,所有5例病例均为B细胞系的血液淋巴肿瘤。这些淋巴瘤由一个B细胞克隆群体组成,该群体表现出体细胞免疫球蛋白和BCL-6突变以及BCL-6蛋白表达。因此,肿瘤性梭形细胞与生发中心的B细胞非常相似。肿瘤性梭形细胞中MUM1表达缺失提示肿瘤性梭形细胞可能与B细胞生发中心内成熟的早期阶段有关。生发中心表型,伴有BCL-6的限制性表达,与原发性结外起源、乳酸脱氢酶水平正常以及对治疗反应良好有关。

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