| Literature DB >> 28571156 |
Ruchee Khanna1, Sushma Belurkar1, P Lavanya2, Chethan Manohar3, Manna Valiathan3.
Abstract
Mantle Cell Lymphoma (MCL) is a type of Non-Hodgkin's lymphoma and has a wide spectrum of histopathological subtypes of which the blastoid or the blastic variant constitutes 10-15% of all cases. It is difficult to diagnose blastoid variant of MCL on the basis of morphology alone as it mimics lymphoblastic lymphoma and centroblastic large cell lymphoma, hence additional analysis like immunophenotyping and molecular studies aid in its diagnosis. We present a case of 45-year-old male who presented to medicine OPD with chief complaints of fever, fatigability and inguinal swelling. Complete blood count, peripheral smear and bone marrow examination was performed. Peripheral smear showed thrombocytopenia along with 53% abnormal cells. On bone marrow examination 43% abnormal lymphoid cells were seen. This case was diagnosed as blastoid variant of MCL on the basis of routine morphology and immunohistochemistry on bone marrow biopsy and flow cytometric immunophenotyping on peripheral blood.Entities:
Keywords: Flow cytometry; Hepatomegaly; Non-Hodgkin’s lymphoma
Year: 2017 PMID: 28571156 PMCID: PMC5449802 DOI: 10.7860/JCDR/2017/24221.9670
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X