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首页> 外文期刊>Virchows Archiv: an international journal of pathology >Indolent lymphomas in the pediatric population: follicular lymphoma, IRF4/MUM1+lymphoma, nodal marginal zone lymphoma and chronic lymphocytic leukemia
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Indolent lymphomas in the pediatric population: follicular lymphoma, IRF4/MUM1+lymphoma, nodal marginal zone lymphoma and chronic lymphocytic leukemia

机译:小儿的惰性淋巴瘤:滤泡性淋巴瘤,IRF4 / MUM1 +淋巴瘤,淋巴结边缘区淋巴瘤和慢性淋巴细胞性白血病

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摘要

Indolent lymphomas in the pediatric population were discussed during the 2014 European Association for Haematopathology/Society of Hematopathology workshop in Istanbul, Turkey. This session was focused on pediatric-type follicular lymphoma (FL), and its differential diagnosis with the newly recognized entity of IRF4/MUM1+ lymphomas mainly involving Waldeyer's ring. The differential diagnosis between t(14;18) negative FL grade 1/2 and pediatric-type FL in adults was highlighted. The overlapping pathological and clinical features between FL and nodal marginal zone lymphoma (NMZL) in children and young adults were recognized and morphologic and immunophenotypical criteria helpful for the differential diagnosis were presented. Both pediatric-type FL and NMZL are indolent processes that should be distinguished from atypical lymphoid hyperplasia of the tonsils and lymph nodes. The demonstration of a B cell monoclonal population by molecular studies is strongly recommended for the diagnosis. Recognition of these indolent variants to avoid overtreatment was emphasized. Whereas most indolent lymphomas in the pediatric population show characteristic clinical, pathologic, and genetic features that differ from the adult counterpart, other rare indolent lymphoid tumors such as chronic lymphocytic leukemia (CLL) have similar characteristics. In this report, novel findings, areas of special interest, and diagnostic challenges emerging from the cases submitted to the workshop will be discussed.
机译:在土耳其伊斯坦布尔举行的2014年欧洲血液病理学/血液病理学学会研讨会上,对儿科人群惰性淋巴瘤进行了讨论。本次会议的重点是小儿型滤泡性淋巴瘤(FL)及其与新发现的主要涉及Waldeyer环的IRF4 / MUM1 +淋巴瘤的鉴别诊断。强调了t(14; 18)1/2级阴性FL与小儿型FL的鉴别诊断。认识到儿童和青年人FL和淋巴结边缘区淋巴瘤(NMZL)之间重叠的病理和临床特征,并提出了有助于鉴别诊断的形态学和免疫表型标准。小儿型FL和NMZL均为惰性过程,应与扁桃体和淋巴结的非典型淋巴样增生区分开。强烈建议通过分子研究证明B细胞单克隆具有诊断意义。强调了识别这些惰性变体以避免过度治疗。小儿人群中大多数惰性淋巴瘤的临床,病理学和遗传学特征均不同于成人,而其他罕见的惰性淋巴瘤如慢性淋巴细胞白血病(CLL)具有相似的特征。在本报告中,将讨论提交研讨会的病例中发现的新发现,特别感兴趣的领域以及诊断难题。

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