Peripheral T-cell Lymphomas of Follicular T-Helper Cell Derivation With Hodgkin/Reed-Sternberg Cells of B-cell Lineage Both EBV-positive and EBV-negative Variants Exist

被引:90
作者
Nicolae, Alina [1 ]
Pittaluga, Stefania [1 ]
Venkataraman, Girish [3 ]
Vijnovich-Baron, Anahi [4 ]
Xi, Liqiang [2 ]
Raffeld, Mark [2 ]
Jaffe, Elaine S. [1 ]
机构
[1] NCI, Hematopathol Sect, Bethesda, MD 20892 USA
[2] NCI, Mol Diagnost Unit, Pathol Lab, Ctr Canc Res, Bethesda, MD 20892 USA
[3] Loyola Univ, Med Ctr, Dept Pathol, Maywood, IL 60153 USA
[4] Ctr Patol CEPACIT, Buenos Aires, DF, Argentina
基金
美国国家卫生研究院;
关键词
peripheral T-cell lymphoma; T follicular helper cells; classical Hodgkin lymphoma; angioimmunoblastic T-cell lymphoma; Epstein-Barr virus; PD-1; CD279; ANGIOIMMUNOBLASTIC LYMPHADENOPATHY; LYMPHOPROLIFERATIVE DISORDERS; GROWTH-PATTERN; DISEASE; PHENOTYPE; TRANSFORMATION; PROLIFERATION; INVOLVEMENT; SURVIVAL; INSIGHTS;
D O I
10.1097/PAS.0b013e3182785610
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Peripheral T-cell lymphomas (PTCLs) are functionally and morphologically complex. Epstein-Barr virus (EBV)-positive B cells have been reported in angioimmunoblastic T-cell lymphoma (AITL) and other PTCLs and may mimic Hodgkin/Reed-Sternberg (HRS) cells, but EBV-negative HRS-like B cells have not been described. We wished to assess the nature of the PTCL associated with HRS-like cells and to determine whether EBV-negative HRS-like cells may be seen. We identified 57 PTCL cases reported as containing HRS-like cells. These included 32 AITL, 19 PTCL, not otherwise specified (NOS), 3 PTCL-NOS, follicular variant, 1 PTCL-NOS, T-zone variant, and 2 adult T-cell leukemia/lymphoma cases. All patients were adults with a median age of 63 and presented with lymphadenopathy. The male: female ratio was 31:26 (1.2:1). Clonal TRG rearrangement was detected in 46/53 cases. Six of 38 cases had a concomitant clonal immunoglobulin gene rearrangement. In 52/57 cases the HRS cells were positive for EBV. Five cases, 3 classified as AITL and 2 as PTCL-NOS, follicular variant, contained HRS-like cells negative for EBV. All PTCLs with EBV-negative HRS cells had a T follicular helper cell immunophenotype. The neoplastic T cells expressed CD3, CD4, and PD-1 and formed rosettes around the HRS-like cells. The HRS-like cells were positive for CD20 (variable intensity), PAX5, CD30, and CD15 (4/5). We conclude that both EBV-positive and EBV-negative HRS-like B cells may occur in the background of PTCL; caution is needed to avoid misdiagnosis as classical Hodgkin lymphoma. The close interaction between the HRS-like cells and the rosetting PD-1-positive T cells suggests a possible pathogenetic role in this phenomenon and provides new insights into the abnormal B-cell proliferations that occur in the context of T-FH malignancies.
引用
收藏
页码:816 / 826
页数:11
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