LETTER TO THE EDITOR Hepatosplenic alpha beta T-cell lymphoma successfully treated with allogeneic bone marrow transplantation

摘要

Hepatosplenic T-cell lyraphoma (HSTCL) is a rare type of peripheral T-cell lymphoma characterized in young adult males by hepatosplenomegaly, B-symptoms, peripheral blood cytopenias and no lymphadenopathy; lymphomatous infiltrates in the splenic red pulp, hepatic sinusoids and bone marrow sinuses; T cell receptor (TCR) gamma delta-chain and cytotoxic T-cell phenotype; isochromosome (i) 7q in conjunction with other abnormalities, most commonly trisomy 8; and aggressive clinical course.