| Literature DB >> 27468978 |
Josephine M Vos1,2, Joshua Gustine1, Helmut G Rennke3,4, Zachary Hunter1, Robert J Manning1, Toni E Dubeau1, Kirsten Meid1, Monique C Minnema5, Marie-Jose Kersten6, Steven P Treon1,4, Jorge J Castillo1,4.
Abstract
The incidence and prognostic impact of nephropathy related to Waldenström macroglobulinaemia (WM) is currently unknown. We performed a retrospective study to assess biopsy-confirmed WM-related nephropathy in a cohort of 1391 WM patients seen at a single academic institution. A total of 44 cases were identified, the estimated cumulative incidence was 5·1% at 15 years. There was a wide variation in kidney pathology, some directly related to the WM: amyloidosis (n = 11, 25%), monoclonal-IgM deposition disease/cryoglobulinaemia (n = 10, 23%), lymphoplasmacytic lymphoma infiltration (n = 8, 18%), light-chain deposition disease (n = 4, 9%) and light-chain cast nephropathy (n = 4, 9%), and some probably related to the WM: thrombotic microangiopathy (TMA) (n = 3, 7%), minimal change disease (n = 2, 5%), membranous nephropathy (n = 1, 2%) and crystal-storing tubulopathy (n = 1, 2%). The median overall survival in patients with biopsy-confirmed WM-related nephropathy was 11·5 years, shorter than for the rest of the cohort (16 years, P = 0·03). Survival was better in patients with stable or improved renal function after treatment (P = 0·05). Based on these findings, monitoring for renal disease in WM patients should be considered and a kidney biopsy pursued in those presenting with otherwise unexplained renal failure and/or nephrotic syndrome.Entities:
Keywords: Waldenström macroglobulinaemia; amyloidosis; epidemiology; haemodialysis; renal medicine
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Year: 2016 PMID: 27468978 DOI: 10.1111/bjh.14279
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998