Santos, TMachado, SSousa, VCampos, M2016-05-112016-05-112015BMJ Case Rep. 2015 Oct 7;2015. pii: bcr2015211210http://hdl.handle.net/10400.4/1896Renal 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.engDoenças do RimMacroglobulinemia de WaldenstromCast nephropathy: an extremely rare renal presentation of Waldenström's macroglobulinaemiajournal article10.1136/bcr-2015-211210