Unusual relapse of an angioimmunoblastic T cell lymphoma 11 years after initial manifestation.

The article presents a case study of a 74-year-old female with lymphadenopathy, fever, and splenomegaly. Topics discussed include results of histological examination of an axillary lymph node which showed atrophic follicles with expanded meshworks of follicular dendritic cells, reports on angimmunoblastic T cell lymphoma (AITL) which is a rare aggressive non-Hodgkin lymphoma and identification of molecular prognosticator.