Suppr超能文献

美国病理学学会专家意见:经典霍奇金淋巴瘤的免疫组化评估。

American Registry of Pathology Expert Opinions: Immunohistochemical evaluation of classic Hodgkin lymphoma.

机构信息

Neogenomics, Inc., 31 Columbia, Aliso Viejo, CA 92656, United States of America.

Memorial/Sloane-Kettering Cancer Center, New York, NY, United States of America.

出版信息

Ann Diagn Pathol. 2019 Apr;39:105-110. doi: 10.1016/j.anndiagpath.2019.02.001. Epub 2019 Feb 6.

Abstract

The diagnosis of classic Hodgkin lymphoma requires immunohistochemical confirmation in most cases and one can argue for these studies as standard-of-care in the diagnostic workup. The authors propose a panel of studies for primary identification of CHL to include: CD3, CD20, CD15, CD30 and PAX5. When pattern discordances are identified, additional assessment is recommended. In the case of overexpression of B lineage markers by Hodgkin/Reed-Sternberg cells, or a differential diagnosis that includes large B-cell lymphoma or variants, additional markers recommended are: CD45, OCT2, BOB1, CD79a and MUM1/IRF4. If primary mediastinal large B cell lymphoma is considered in the differential diagnosis, suggested additional markers include: P63, CD23, CD45 and CD79a. When considering a differential diagnosis that includes anaplastic large cell lymphoma we suggest: ALK, CD45, pan T cell antigens (such as CD2, CD5, CD7, and CD43), and cytotoxic markers (granzyme, perforin, and TIA1). If peripheral T cell lymphoma or T cell lymphomas of follicular helper origin are considered in the differential diagnosis, the following panel is recommended: pan T cell antigens, CD4, CD8, one or more follicular dendritic cell markers, and assessment for Epstein-Barr virus (EBV) infection, preferably EBV encoded RNA (EBER) as assessed by in situ hybridization When the differential diagnosis includes nodular lymphocyte predominant Hodgkin lymphoma, recommended additional studies include OCT2, CD21 and/or CD23, PD1, and assessment for EBV infection. The authors recognize that these panels may not be adequate to completely characterize other lymphomas, but these panels will usually be sufficient to distinguish classic Hodgkin lymphoma from other lymphoma types.

摘要

经典型霍奇金淋巴瘤的诊断在大多数情况下需要免疫组织化学确认,因此可以将这些研究作为诊断工作的标准。作者提出了一组研究来初步确定 CHL,包括:CD3、CD20、CD15、CD30 和 PAX5。当发现模式不一致时,建议进行额外的评估。在霍奇金/里德-斯特恩伯格细胞过度表达 B 细胞标记物或包括大 B 细胞淋巴瘤或变体的鉴别诊断的情况下,建议增加以下标记物:CD45、OCT2、BOB1、CD79a 和 MUM1/IRF4。如果在鉴别诊断中考虑原发性纵隔大 B 细胞淋巴瘤,则建议增加以下标记物:P63、CD23、CD45 和 CD79a。当考虑包括间变性大细胞淋巴瘤的鉴别诊断时,我们建议增加:ALK、CD45、泛 T 细胞抗原(如 CD2、CD5、CD7 和 CD43)和细胞毒性标记物(颗粒酶、穿孔素和 TIA1)。如果在鉴别诊断中考虑外周 T 细胞淋巴瘤或滤泡辅助起源的 T 细胞淋巴瘤,则建议使用以下面板:泛 T 细胞抗原、CD4、CD8、一个或多个滤泡树突状细胞标记物,并评估 EBV 感染,最好通过原位杂交评估 EBV 编码 RNA(EBER)。当鉴别诊断包括结节性淋巴细胞为主型霍奇金淋巴瘤时,建议增加 OCT2、CD21 和/或 CD23、PD1 的研究,并评估 EBV 感染。作者认识到这些面板可能不足以完全描述其他淋巴瘤,但这些面板通常足以将经典型霍奇金淋巴瘤与其他淋巴瘤类型区分开来。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验