Double-Hit Lymphoma Presenting as Primary Renal Lymphoma: A Case Report

Journal Title: Journal of Interdisciplinary Histopathology - Year 2013, Vol 1, Issue 2

Abstract

B-cell lymphomas with concurrent MYC with BCL2 and/or BCL6 rearrangements, also known as “double hit” lymphomas (DHL), are rare neoplasms characterized by highly aggressive clinical behavior, complex karyotypes, and a spectrum of pathological features overlapping with Burkitt lymphoma (BL) and diffuse large B-cell lymphoma (DLBCL). Primary renal lymphoma (PRL) by definition is a renal lymphoma without evidence of systemic involvement. PRL is extremely rare with less than 100 cases of both Hodgkin disease and non-Hodgkin lymphoma reported in literature. Double hit lymphomas have extremely poor prognosis, and high resistance to intensive chemotherapy, including high-dose chemotherapy. We describe a very rare case of DHL arising in kidney as PRL in whom concurrent MYC and IGH-BCL2 rearrangements were detected.

Authors and Affiliations

Vikas Mehta, Chandy Ellimottil, Jodi Speiser, Milind Velankar, Güliz Barkan

Keywords

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  • EP ID EP135611
  • DOI 10.5455/jihp.20130121075815
  • Views 77
  • Downloads 0

How To Cite

Vikas Mehta, Chandy Ellimottil, Jodi Speiser, Milind Velankar, Güliz Barkan (2013). Double-Hit Lymphoma Presenting as Primary Renal Lymphoma: A Case Report. Journal of Interdisciplinary Histopathology, 1(2), 93-97. https://europub.co.uk/articles/-A-135611