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使用组织学和免疫组织化学特征评估慢性淋巴细胞白血病/小淋巴细胞淋巴瘤的加速和转化:病例系列。

Assessment for acceleration and transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma using histologic and immunohistochemical features: a case series.

机构信息

Department of Pathology and Laboratory Medicine, University of Virginia, 1215 Lee Street, 3rdFloor Hospital Expansion, Charlottesville, VA, 22908, USA.

出版信息

J Hematop. 2024 Sep;17(3):139-147. doi: 10.1007/s12308-024-00598-3. Epub 2024 Jul 23.

Abstract

Morphologic features of aggressive/ "accelerated" chronic lymphocytic leukemia/small lymphocytic lymphoma (aCLL/SLL) have been described. Richter transformation (RT) also occurs in a subset of CLL/SLL cases. This case series examined inter-observer variability when assessing for aCLL/SLL and RT, with attention to how immunohistochemical (IHC) markers may assist in this evaluation. Twelve cases of CLL/SLL with available FFPE tissue were identified. H&E staining and IHC (CD3, CD20, CD5, CD23, LEF1, LAG3, C-MYC, PD-1, MUM1, Cyclin D1, BCL-6, p53, and Ki-67) were performed. Three hematopathologists reviewed each case. The pathologists provided a final interpretation of (1) CLL/SLL, (2) CLL/SLL with expanded and/or confluent proliferation centers or increased Ki-67 (aCLL/SLL), or (3) large cell transformation/DLBCL. The pathologists lacked consensus in the diagnosis in 6/12 cases (50%). The reviewers disagreed on the presence of expanded/confluent proliferation centers in 8/12 cases (67%). With the exception of Ki-67, no IHC marker showed a difference in the staining profile in aCLL/SLL or RT compared to low-grade cases. This series showed inter-observer variability in the evaluation for aCLL/SLL and RT. A study that serially examines genetic alterations in FFPE tissue and correlates the features with histology and IHC, at diagnosis and throughout the disease course, may help refine indicators of aggressive disease.

摘要

侵袭性/“加速”慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(aCLL/SLL)的形态学特征已有描述。Richter 转化(RT)也发生在一部分 CLL/SLL 病例中。本病例系列研究了评估 aCLL/SLL 和 RT 时的观察者间变异性,并关注免疫组织化学(IHC)标志物如何协助这一评估。确定了 12 例具有可用 FFPE 组织的 CLL/SLL 病例。进行了 H&E 染色和 IHC(CD3、CD20、CD5、CD23、LEF1、LAG3、C-MYC、PD-1、MUM1、Cyclin D1、BCL-6、p53 和 Ki-67)。三位血液病理学家审查了每个病例。病理学家对(1)CLL/SLL、(2)具有扩大和/或融合性增殖中心或 Ki-67 增加的 CLL/SLL(aCLL/SLL),或(3)大细胞转化/DLBCL 提供最终解释。在 6/12 例(50%)病例中,病理学家的诊断不一致。在 8/12 例(67%)病例中,审查者对是否存在扩大/融合性增殖中心存在分歧。除了 Ki-67 之外,没有任何 IHC 标志物在 aCLL/SLL 或 RT 与低级别病例的染色模式上显示出差异。本系列研究表明,在评估 aCLL/SLL 和 RT 时存在观察者间变异性。一项在 FFPE 组织中连续检查遗传改变并将特征与组织学和 IHC 相关联的研究,在诊断时和整个疾病过程中,可能有助于细化侵袭性疾病的指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ae/11324784/593170f1085b/12308_2024_598_Fig1_HTML.jpg

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