Angioimmunoblastic T-Cell Lymphoma Diagnosed From Serous Effusion by Integration of Cytologic Features and Ancillary Studies

Abstract Objectives To explore the approach to the diagnosis of malignant serous effusion (SE) caused by angioimmunoblastic T-cell lymphoma (AITL). Methods The clinical, cytomorphologic, immunophenotypic, and molecular features of 6 patients were summarized. Results Clinically, SE caused by AITL was...

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Published inAmerican journal of clinical pathology Vol. 159; no. 4; pp. 379 - 394
Main Authors Li, Jinnan, Zhu, Xianglan, Deng, Xueqin, Zhang, Wenyan, Jiang, Yong, Wan, Yin, Chen, Jie, Li, Cong, Liu, Weiping, Zhao, Sha, Su, Xueying
Format Journal Article
LanguageEnglish
Published US Oxford University Press 04.04.2023
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Summary:Abstract Objectives To explore the approach to the diagnosis of malignant serous effusion (SE) caused by angioimmunoblastic T-cell lymphoma (AITL). Methods The clinical, cytomorphologic, immunophenotypic, and molecular features of 6 patients were summarized. Results Clinically, SE caused by AITL was predominant in middle-aged and older male patients with multiple SEs and lymphadenopathy. Cytomorphology showed small to medium-sized, irregular lymphocytes with clear cytoplasm and mixed with various inflammatory cells and apoptosis. Hodgkin/Reed-Sternberg–like cells were detected in 2 of 6 cases. Furthermore, 2 patterns of cytomorphology were described for the first time. Flow cytometry revealed abnormal T-cell populations with loss of surface CD3 (3/4 cases) and CD7 (3/4 cases). In addition, B-cell populations lacking surface immunoglobulin (Ig) were identified in 2 of 4 cases. Immunocytochemical staining revealed expression of at least 2 T follicular helper markers. Epstein-Barr virus–encoded RNA (EBER)–positive cells were demonstrated in 4 of 5 cases. Clonal T-cell receptor γ chain rearrangement was detected in 6 cases, and 3 of them had concomitant clonal immunoglobulin gene rearrangement. Moreover, 2 cases revealed discrepant findings regarding IgH/Igκ rearrangements in cytohistologic correlation. Conclusions This study broadens the morphologic spectrum of malignant SE caused by AITL and provides diagnostic criteria in routine practice.
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ISSN:0002-9173
1943-7722
DOI:10.1093/ajcp/aqac170