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Abstract: PO1939

Patients with Active Mantle Cell Lymphoma May Present with Monoclonal, Polyclonal, or C3-Dominant Glomerulonephritides, Which Respond to Lymphoma-Directed Therapy

Session Information

Category: Pathology and Lab Medicine

  • 1600 Pathology and Lab Medicine

Authors

  • Andeen, Nicole K., Oregon Health & Science University, Portland, Oregon, United States
  • Abdulameer, Shahad, University of Washington, Seattle, Washington, United States
  • Charu, Vivek, Stanford University, Stanford, California, United States
  • Zuckerman, Jonathan E., University of California Los Angeles, Los Angeles, California, United States
  • Troxell, Megan L., Stanford University, Stanford, California, United States
  • Kambham, Neeraja, Stanford University, Stanford, California, United States
  • Alpers, Charles E., University of Washington, Seattle, Washington, United States
  • Najafian, Behzad, University of Washington, Seattle, Washington, United States
  • Nicosia, Roberto F., University of Washington, Seattle, Washington, United States
  • Smith, Kelly D., University of Washington, Seattle, Washington, United States
  • Kung, Vanderlene Liu, Oregon Health & Science University, Portland, Oregon, United States
  • Avasare, Rupali S., Oregon Health & Science University, Portland, Oregon, United States
  • Yamashita, Michifumi, Cedars-Sinai Medical Center, Los Angeles, California, United States
  • Bissonnette, Mei Lin, The University of British Columbia, Vancouver, British Columbia, Canada
  • Akilesh, Shreeram, University of Washington, Seattle, Washington, United States
  • Hou, Jean, Cedars-Sinai Medical Center, Los Angeles, California, United States
Background

There are limited reports on kidney biopsy findings in patients with mantle cell lymphoma (MCL).

Methods

We initiated a multi-institutional, retrospective review of kidney biopsy findings from patients with active and treated MCL.

Results

Twenty-nine patients (31 biopsies) with MCL and kidney biopsies were identified, with a median age of 66 (range 48-87), 76% of whom were men. Nineteen patients had active MCL at the time of biopsy, 13 of which (68%) presented with acute kidney injury, proteinuria and/or hematuria, and biopsy findings attributable to lymphoma (Table); 6 (32%) had findings not readily attributable to MCL. Of the former, 10 (77%) had immune complex (IC) disease including proliferative glomerulonephritis with monotypic Ig deposits (PGNMID, 2), C3 dominant GN (3), PLA2R-negative membranous (MN, 3), and/or tubular basement membrane deposits (2). Lymphomatous infiltration was present in 6, 3 with coincident IC lesions. Four with available follow-up were treated for MCL, all with remission of GN (1 PGNMID, 2 C3 dominant GN, 1 MN). Ten patients were biopsied while MCL was in remission; these findings were attributed to various underlying diseases.

Conclusion

In patients with active MCL who undergo kidney biopsy, 68% had kidney biopsy findings attributable to lymphoma. Diverse immune complex diseases were seen in ~50%, including monoclonal, polyclonal, and C3 dominant GN patterns, and nearly 1/3rd had lymphomatous infiltration. Limited follow-up suggests these IC lesions respond to MCL-directed therapy.