Angioimmunoblastic T-cell lymphoma associated with leukocytosis and lymphocytosis; a case report and systematic review
نویسندگان
1 Regenerative medicine, organ procurement and transplantation multi-disciplinary center, Razi hospital, school of medicine, Guilan university of medical sciences, Rasht, Iran; drsaeidanvari@gmail.com
2 Student research committee, school of paramedical sciences, Guilan university of medical sciences, Rasht, Iran
3 Department of Internal Medicine, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran;
4 Department of Hematology and Blood Banking, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
5 Clinical laboratory sciences department, School of Paramedical Sciences, Guilan University of Medical Sciences, Rasht, Iran
6 Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
doi
10.58209/ijbc.15.1.36چکیده
Background: Angioimmunoblastic T-cell lymphoma (AITL) is an uncommon lymphoma arising from follicular T-helper cells. Since this is a rare disease, diagnosis is unfortunately difficult. AITL responds to treatments, therefore by reviewing the characteristics of the available cases, we aimed to classify the available data for in-time diagnosis. Objectives and data sources: ...
