The study investigates the clinical features and treatment of a rare condition called CD4CD8 T-cell large granular lymphocytic leukemia (T-LGLL) through a case report.
A 70-year-old woman was diagnosed and exhibited symptoms like low platelet counts and myelodysplasia, with blood tests showing an abundance of large granular lymphocytes.
Treatment involving cyclophosphamide and prednisone led to partial remission, highlighting the unique clinical characteristics of CD4CD8 T-LGLL compared to other forms.