Angioimmunoblastic T-cell lymphoma:a case report and review of literature

Objective To raise awareness of angioimmunoblastic T-cell lymphoma (AITL) by one case of AITL and review of literature reports.Methods The clinic and follow-up data of one patient with AITL were analyzed,and clinical features,diagnosis and treatment of AITL were discussed combining with literature.Results AITL is derived from centro-follicular T-helper cells.It is characterized by generalized lymphacenopathy,fever,skin rash,anemia and autoimmune features are frequently described. The diagnosis of AITL needs clinical syndrome and morphology.Despite treatment with polychemotherapy,the prognosis is poor.Conclusions Peripheral nodes pressing hronchia in AITL patients may induce cough.System physical examination helps to reduce misdiagnosis. Key words: Cough variation asthma; Angioimmunoblastic T-cell lymphoma