4.3 Article

Markers of Follicular Helper T Cells Are Occasionally Expressed in T-Cell or Histiocyte-Rich Large B-Cell Lymphoma, Classic Hodgkin Lymphoma, and Atypical Paracortical Hyperplasia A Diagnostic Pitfall For T-Cell Lymphomas of T Follicular Helper Origin

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AMERICAN JOURNAL OF CLINICAL PATHOLOGY
卷 156, 期 3, 页码 409-426

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OXFORD UNIV PRESS INC
DOI: 10.1093/ajcp/aqaa249

关键词

Follicular helper T cells; T-cell or histiocyte-rich large B-cell lymphoma; Atypical paracortical hyperplasia; Classic Hodgkin lymphoma; T-cell lymphomas of T follicular helper origin; PD-1; CXCL13; ICOS; BCL-6; CD10

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  1. Department of Pathology, University of Iowa Hospitals and Clinics

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The study found that AITL more frequently coexpressed more than 2 TFH markers, while PTCL-NOS and PTCL-TFH did not show this phenomenon. The expression of TFH markers also varied in different backgrounds. Caution should be exercised when diagnosing AITL.
Objectives: Follicular helper T cell (TFH) markers are expressed in angioimmunoblastic T-cell lymphoma (AITL) and peripheral T-cell lymphoma of the TFH phenotype (PTCL-TFH). However, differential expression and coexpression of these markers in benign and other malignant lymphoid proliferations have not been well studied. Methods: We performed programmed death-1 (PD-1), C-X-C motif chemokine ligand 13 (CXCL13), inducible costimulator (ICOS), CD10, and B-cell lymphoma 6 protein (BCL-6) immunohistochemistry on AITL, PTCL not otherwise specified (PTCL-NOS), PTCL-TFH, T-cell or histiocyte-rich large B-cell lymphoma (THRLBCL), classic Hodgkin lymphoma (CHL), atypical paracortical hyperplasia (PCH), progressive transformation of germinal centers (PTGC), and reactive follicular hyperplasia (RFH). Results: CXCL13 and ICOS were more sensitive but less specific for AITL than PD-1, CD10, and BCL6. Moreover, 74% of AITL (none of PTCL-NOS or PTCL-TFH) coexpressed more than 2 TFH markers. In background T cells of THRLBCL, 70% of cases coexpressed more than 1 marker. The background T cells of CHL expressed all TFH markers except CD10 in all cases. In addition, 13% of PCH cases coexpressed more than 1 marker. In RFH and PTGC, all markers were expressed mainly in germinal centers with rare extrafollicular staining. Conclusions: AITL, PTCL-NOS, and PTCL-TFH show differential expression of TFH markers. AITL frequently coexpresses more than 2 TFH markers. TFH markers can be expressed in PCH and in background T cells of THRLBCL and CHL. Consequently, caution should be used before a diagnosis of AITL is established, particularly with limited samples.

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