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首页> 外文期刊>Journal of clinical and experimental hematopathology : >Atypical Interfollicular Hyperplasia of Tonsils Resembling Mucosa-Associated Lymphoid Tissue Lymphoma: A Clinicopathological, Immunohistochemical Study and Epstein-Barr Virus Findings in 12 Cases
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Atypical Interfollicular Hyperplasia of Tonsils Resembling Mucosa-Associated Lymphoid Tissue Lymphoma: A Clinicopathological, Immunohistochemical Study and Epstein-Barr Virus Findings in 12 Cases

机译:扁桃体类似黏膜相关淋巴样组织淋巴瘤的非典型小叶间增生:12例临床病理,免疫组织化学研究和爱泼斯坦-巴尔病毒的发现。

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This study attempted to clarify the clinicopathological and immunohistochemical findings and presence or absence of Epstein-Barr virus (EBV) in tonsillar atypical interfollicular hyperplasia (AIFH). A total of 597 consecutive specimens from tonsillectomies performed in Dokkyo University School of Medicine between 1999 and July 2013 were reexamined. Using formalin-fixed, paraffin-embedded sections, histological and immunohistochemical analyses, and in situ hybridization (ISH) were performed. AIFH was identified in the tonsils in 12 (2.0%) cases. These included 7 males and 5 females, aged 3 to 19 years (mean, 7). Histologically, there was expansion of the interfollicular areas by polymorphous infiltration resulting in distortion, but not obliteration of the normal tonsillar architecture. In some areas, the lymphoid follicles had hyperplastic germinal centers with ill-defined borders surrounded by sheet-like proliferation of polymorphous infiltrate showing a marginal zone distribution pattern. The infiltrate was composed of small to medium-sized (transformed) lymphocytes and immunoblasts accompanied by numerous plasma cells and plasmacytoid cells, and resembling monocytoid B cells. The numerous immunoblasts were MUM1+, CD10-, BCL-6-. An ISH study demonstrated EBV-encoded small RNA-1 (EBER-1)+ cells in 9 lesions. Moreover, in 3 lesions, numerous EBER-1+ cells were present in germinal centers as well as in interfollicular areas. The present study indicated that EBV may cause at least a portion of tonsillar AIFH in children and adolescents. In conclusion, an atypical lymphoid infiltration resulting in distortion of tonsillar architecture with numerous MUM1+, CD10-, BCL-6- immunoblasts should raise the suspicion of a reactive process. [ J Clin Exp Hematop 54(2) : 111-116, 2014 ]
机译:这项研究试图阐明扁桃体非典型滤泡间增生(AIFH)的临床病理学和免疫组化发现以及爱泼斯坦-巴尔病毒(EBV)的存在与否。在1999年至2013年7月期间,对独岛大学医学院进行的总共597例扁桃体切除术连续标本进行了重新检查。使用福尔马林固定,石蜡包埋的切片,进行组织学和免疫组化分析,以及原位杂交(ISH)。在扁桃体中发现了12例(2.0%)的AIFH。其中包括7例男性和5例女性,年龄3至19岁(平均7岁)。在组织学上,多晶型浸润使小孔间区域扩大,导致变形,但没有消除正常的扁桃体结构。在某些区域,淋巴滤泡具有增生的生发中心,边界不明确,被多态性浸润物的片状增殖所包围,显示出边缘区分布模式。浸润液由小到中型(转化的)淋巴细胞和免疫母细胞组成,并伴有大量浆细胞和浆细胞样细胞,并类似于单核细胞B细胞。大量免疫原是MUM1 + ,CD10 -,BCL-6 -。 ISH研究表明,EBV编码的小RNA-1(EBER-1) + 细胞在9个病灶中。此外,在3个病灶中,生发中心和卵泡间区域均存在大量的EBER-1 + 细胞。本研究表明,EBV可能导致儿童和青少年的扁桃体AIFH至少引起一部分。总之,非典型淋巴样浸润会导致扁桃体结构变形,并伴有大量MUM1 + ,CD10 -,BCL-6 -免疫母细胞。怀疑反应过程。 [J Clin Exp Hematop 54(2):111-116,2014]

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