| Literature DB >> 26446315 |
Tânia Santos1, Susana Machado1, Vítor Sousa2, Mário Campos1.
Abstract
Renal involvement in Waldenström's macroglobulinaemia (WM) is very unusual when compared to multiple myeloma. We report a case of a patient who developed anuric acute kidney injury secondary to cast nephropathy, dependent on high-flux haemodialysis. Complementary study revealed the presence of blood IgM monoclonal gammopathy and a massive bone marrow lymphoplasmacytic infiltration. There were no osteolytic lesions and no clinical signs/symptoms of hyperviscosity syndrome. The diagnosis of WM was established and a dexamethasone plus cyclophosphamide regime was started, in addition to plasmapheresis. The patient partially recovered renal function allowing haemodialysis and plasmapheresis withdrawal. He remained asymptomatic with a good response to chemotherapy and 12 months after his renal function remained stable. This is a rare clinical case in which WM presented as an IgM cast nephropathy, which in turn is an extremely rare renal presentation of this equally rare haematological disorder. 2015 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2015 PMID: 26446315 PMCID: PMC4600820 DOI: 10.1136/bcr-2015-211210
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X