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DLBCL-Richter transformation in CLL

DLBCL-Richter transformation in CLL
#00061042
Author: Huan-You Wang
Category: Lymphoma: Mature B-cell and Plasma cell Neoplasms > Low-grade B-cell lymphoma > Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma > Richter Transformation > DLBCL variant-RT
Published Date: 05/06/2017

Cervical lymph node (LN) dissection for squamous cell carcinoma was performed on a 69-year-old man in whom chronic lymphocytic leukemia (CLL) was diagnosed in 2004. Fluorescence in situ hybridization determined that the CLL had an ATM deletion. Prior to surgery, the patient experienced a 30-lb (∼14-kg) unintentional weight loss and diffuse lymphadenopathy.

The LN shows numerous discrete foci (inner portion) to confluent (periphery) areas composed of medium to large atypical lymphoid cells in the background of small lymphocytic lymphoma (SLL) (panels A-B; hematoxylin and eosin stain, original magnifications ×20 [A] and ×400 [B]).

These atypical large lymphoid cells are positive for CD20 (panel C, bright; original magnification ×40) with aberrant coexpression of CD5 (panel D, dim; original magnification ×200) compared with negative CD3 (panel E; original magnification ×200). In contrast to surrounding SLL, these atypical large lymphoid cells display ∼60% proliferation index by Ki-67 in both confluent (panel F; original magnification ×20) and nodular regions (panels F-G; original magnifications ×20 [F] and ×200 [G]). Interestingly, the large atypical cells express C-MYC (panel H; original magnification ×200) and MUM1 (panel I; original magnification ×20).

The overall findings are most compatible with the large B-cell lymphoma (LBCL) variant of Richter transformation (RT).