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T-Cell/Histiocyte Rich Large B-Cell Lymphoma –A Case Series with Review of Literature

机译:T细胞/组织细胞丰富的大型B细胞淋巴瘤–病例系列并文献复习

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T-Cell/Histiocyte Rich Large B-Cell Lymphoma (THRLBCL) is a rare variant of Diffuse Large B Cell Lymphoma (DLBCL). This entity differs from the classical DLBCL in the morphology as well as immunohistochemical expression of various CD markers. This lymphoma is characterized by paucity of large, atypical B-cells and surrounded in the background by a dense population of reactive T-cells and histiocytes. This lymphoma gains importance in differentiation from the classical DLBCL in that it is morphologically very similar to the Nodular Lymphocyte Predominant Hodgkin lymphoma (NLPHL). THRBCL is often refractory to the current line of treatment available. Hence, identification of this entity with the help of immuohistochemical and molecular studies is essential for the correct diagnosis and management. Here in this study, we report a series of four cases which are diagnosed as THRLBCL along with review of the literature.
机译:富含T细胞/组织细胞的大型B细胞淋巴瘤(THRLBCL)是弥漫性大型B细胞淋巴瘤(DLBCL)的罕见变体。该实体在各种CD标记物的形态以及免疫组化表达方面不同于经典的DLBCL。这种淋巴瘤的特点是缺乏大量的非典型B细胞,在背景中被大量反应性T细胞和组织细胞包围。该淋巴瘤在形态学上与结节性淋巴细胞优势霍奇金淋巴瘤(NLPHL)非常相似,因此在区别于经典DLBCL方面具有重要意义。 THRBCL通常对当前可用的治疗方法无效。因此,在免疫组织化学和分子研究的帮助下鉴定该实体对于正确的诊断和治疗至关重要。在本研究中,我们将报告一系列被诊断为THRLBCL的四例病例,并复习文献。

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