| Literature DB >> 27656456 |
Pranav Dorwal1, Ritesh Sachdev2, Amit Pande3, Dharmendra Jain4, Bhawna Jha1, Vimarsh Raina5.
Abstract
Hepatosplenic T-cell lymphoma is a rare haematopoietic malignancy that comprises less than 1% of Non-Hodgkin lymphomas. We are reporting a case of a 26-year-old female, who presented with pallor, weight loss, jaundice, pancytopenia and hepatosplenomegaly. The bone marrow examination showed infiltration by lymphoid cells. These cells on flow cytometric evaluation showed the phenotype of hepatosplenic T cell lymphoma. The cells were positive for CD3, CD8, CD56 and TCR γδ and negative for CD5, CD4, CD8, CD16, CD57, TCRαβ along with B cell markers. This case is reported for being a rare clinical entity and its presence in an immunocompetent female making it rarer.Entities:
Keywords: Cluster of differentiation; Hepatosplenomegaly; Immunophenotyping; Pancytopenia
Year: 2016 PMID: 27656456 PMCID: PMC5028430 DOI: 10.7860/JCDR/2016/16943.8355
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X