Image Description
CD20+ and CD79a+ B-cells are present in varying numbers either scattered singly or in follicular aggregates in angioimmunoblastic T-cell lymphoma.
The B cells are small but become large and blast-like when infected with EBV. Latent membrane protein 1 (LMP1) is positive by immunohistochemistry in 30% to 50% of cases; however, EBER is more sensitive for detecting the EBV (see next two images)
About the Disease
Angioimmunoblastic T-cell lymphoma (AITL) is a type of peripheral T-cell lymphoma arising from follicular helper T cells of the germinal center. It is a systemic disease that presents with generalized lymphadenopathy, hepatosplenomegaly, constitutional symptoms, skin rash, anemia, and polyclonal hypergammaglobulinemia. There is effacement of the normal nodal architecture with disappearance of follicles and germinal centers, a polymorphic cellular infiltrate that extends into perinodal tissues, and proliferation of high endothelial venules and follicular dendritic cells. The atypical T-cells have irregular nuclei and clear cytoplasm. Epstein-Barr virus (EBV) can be detected by in-situ hybridization in 80% to 90% of lymph nodes affected by AITL. The virus is present in transformed B-cells and is not considered to play a role in the pathogenesis. The T-cell receptor genes are clonally rearranged. AITL is a rapidly progressive disease with a median survival of under 3 years. Given the abnormal T-cell function and the immunodeficient state, the cause of death in most cases is complications from infectious diseases. Many patients with AITL also develop EBV+ diffuse large B-cell lymphoma. References:Jaffe, E. S. et al (2017). Hematopathology - Second Edition. Philadelphia, PA. Elsevier. Swerdlow S. H. et al (2017). WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Revised 4th Edition. Lyon, France.