Journal article
Treatment of patients with Waldenström macroglobulinaemia: clinical practice guidelines from the Myeloma Foundation of Australia Medical and Scientific Advisory Group
D Talaulikar, CS Tam, D Joshua, JP Ho, J Szer, H Quach, A Spencer, S Harrison, P Mollee, AW Roberts, N Horvath, C Lee, A Zannettino, R Brown, B Augustson, W Jaksic, J Gibson, A Kalff, A Johnston, J Trotman Show all
Internal Medicine Journal | WILEY | Published : 2017
DOI: 10.1111/imj.13311
Abstract
Waldenström macroglobulinaemia (WM) is an indolent B-cell malignancy characterised by the presence of immunoglobulin M (IgM) paraprotein and bone marrow infiltration by clonal small B lymphocytes, plasmacytoid lymphocytes and plasma cells. The symptoms of WM are protean, often follow an asymptomatic phase and may include complications related to the paraneoplastic effects of IgM paraprotein. The revised 2016 World Health Organization classification includes the MYD88 L265P mutation, which is seen in >90% of cases, within the diagnostic criteria for WM. While treatment of WM has often been considered together with other indolent B cell lymphomas, there are unique aspects of WM management that..
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