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金秋獻禮,共慶雙節(jié)|一份實用的血液腫瘤免疫表型參考圖表,請收好!


免疫表型(Immunophenotype)是指細胞表面、細胞內或分泌的蛋白質(主要是抗原)的表達模式。不同的細胞系列(如淋巴細胞、髓系細胞)和細胞發(fā)育的不同階段,都會表達獨特的CD抗原組合。
免疫表型檢測,在臨床實踐中通常通過流式細胞術(Flow Cytometry)或免疫組化(Immunohistochemistry)來實現,是現代血液腫瘤診療中不可或缺的核心技術之一。它被譽為血液病醫(yī)生的“火眼金睛",其作用貫穿于血液腫瘤的診斷、分型、預后判斷和治療監(jiān)測的全過程。
上周我們更新了一篇非淋系的WHO-HAEM5(第5版造血與淋巴組織腫瘤分類)的疾病名稱中英文對照。

第5版WHO造血淋巴腫瘤疾病名稱中英文對照—非淋系篇
這周我們來看一下,根據WHO-HAEM5(第5版造血與淋巴組織腫瘤分類),而制作的免疫表型的表達圖譜,供血液從業(yè)者日常使用參考。
免疫表型的表達圖譜
(點擊圖片查看高清大圖)





說明
(上下滑動閱覽)
- Waldenstr?m macroglobulinema (ICD-O code=9761/3) is found in a significant subset of patients with lymphoplasmacytic lymphoma with BM involvement and an IgM monoclonal gammopathy of any concentration. 
- In Heavy Chain Diseases, intracellular Ig heavy chains are not always IgMs. 
- Typically IgM+, and less often IgA+ or IgG+. 
- IgD is positive in a minority of the cases. 
- IgM+/-, IgD, IgG or rarely IgA. 
- More frequently with Lambda than Kappa restriction. 
- The membrane expression of CD3 may be weak. 
- 25% of patients coexpress CD8 with CD4, a feature almost unique to T-PLL. 15% are CD4-neg, CD8-pos. 
- Expression of CD94/NKG2 and KIR families of receptors can be detected in 50% or more of cases. 
- Uncommon variants include CD4 TCRα/β-pos cases and TCRγ/δ-pos cases. Approximately 60% of the latter express CD8, the remainder are CD4/CD8-neg. 
- Abnormal uniform expression of CD8 can be seen. 
- KIR-pos cases preferentially express activating receptor isoforms. 
- If TCRα/β-positive, expect dierent immunophenotype for the rest of the markers. 
- A CD4-pos/CD8-neg phenotype predominates in nodal cases. CD4/CD8 double positivity or double negativity is at times seen. 
- CD13 with heterogeneous expression. 
- Co-expression of CD15 and strong CD64 is characteristic of monocytic dierentiation. 
- CD25 is highly associated with t(9;22) B-ALL, at least in adults. 
- NG2 is characteristically expressed and is relatively, though not absolutely, specific. 
- The cortical T stage shows a double positive (CD4-pos/CD8-pos) phenotype. The medullary T stage expresses only either CD4 or CD8. 
- IgM+/IgD+ as for B-CLL/SLL 
- When t(14;18) IGH/BCL2 is present, bcl2 expression is bright 
- >90% of cases also express Sox-11 by IHC 
- MYC protein is strongly expressed due to translocation of the MYC gene to the IGH, IGK, or IGL genes. 
- All immunophenotypes for T-ALL/T-LBL are based on IHC and NOT flow cytometry 
- In AML with inv(16), CD14 and CD64 are mainly expressed by the monocytic component of this AML with myelomonocytic dierentiation, and CD16 is mainly expressed by the granulocytic component 
- In AML with t(15;17), CD2, CD34, and CD123 are most commonly expressed by the microgranular variant 
- In AML with NPM1 mutation, the immunophenotype diers between cases with prominent monocytic dierentiation and cases with prominent myeloblastic morphology (the latter often has cuplike nuclear invagination if a concurrent FLT3-ITD mutation is present) 
- AML with RAM phenotype, a subset of megakaryoblastic AML, expresses high-level CD56 without CD7 



掃碼登記即可下載資料
參考文獻(上下滑動閱覽)

1. WHO Classification of Tumours Editorial Board. Haematolymphoid tumours. Lyon (France): International Agency for Research on Cancer; 2024.
2. Jae ES, Harris NL, Stein H, et al. Dendritic cell neoplasms: A review of the current classification. Am J Surg Pathol.
2022;46(1):100-112.
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4. Zhang L-F, Zhang Y, Shui R-H, et al. MNDA expression and its value in dierential diagnosis of B-cell non-Hodgkin lymphomas: a comprehensive analysis of a large series of 1293 cases. Diagn Pathol. 2024;19:60.
5. Choi JY, Lee JH, Yang WI. Reactive lymphoid hyperplasia in the lymph nodes of patients with lymphoma. Pathol Res Pract. 2021;217:153296.
6. Fujimoto M, Kikuchi M. Kikuchi's disease: the history and the current understanding of the disease. Ann Hematol.
2019;98(3):553-560.
7. Stone JH, Zen Y, Deshpande V. IgG4-related disease. N Engl J Med. 2012;366(6):539-551.
8. Wang Q, Liu H, Liu Q, et al. The clinical features of unicentric and multicentric Castleman disease: a single-center experience. Hematol Oncol. 2021;39(3):314-321.
9. Polizzotto MN, Uldrick TS, Wang V, et al. Kaposi sarcoma–associated herpesvirus (human herpesvirus 8) and the etiology of multicentric Castleman disease. Blood. 2019;133(11):1186-1197.
10. Geyer JT, Medeiros LJ, et al. Indolent T-lymphoblastic proliferation: A diagnostic dilemma. Mod Pathol. 2015;28(4):527-535.
11. Ponniah R, Chua I, et al. The challenges of diagnosing autoimmune lymphoproliferative syndrome. J Clin Pathol. 2018;71(7):651-658.
12. Krenacs T, et al. Rosai-Dorfman disease: A comprehensive review. Leuk Lymphoma. 2020;61(7):1534-1542.


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