| Literature DB >> 25363150 |
Stephanie Harel1, Melanie Mohr, Isabelle Jahn, Francoise Aucouturier, Lionel Galicier, Bouchra Asli, Marion Malphettes, Raphael Szalat, Jean-Claude Brouet, Dan Lipsker, Jean-Paul Fermand.
Abstract
This retrospective analysis was conducted in 64 patients diagnosed with type I cryoglobulinaemia (CG) followed at two French centres. Median follow-up was 6·75 years. CG was IgG in 60% and IgM in 40% of all cases and was asymptomatic in 16 patients (25%). Cold-triggered ischaemic skin manifestations were observed in 33 patients (51%). Neurological manifestations were observed in 15 patients and renal manifestations in 13. Most of the patients with necrotic purpura (14/16, P = 0·009) and renal manifestations (11/13, P = 0·057) had IgG CG. IgG CG was associated with monoclonal gammopathy of undetermined significance (MGUS), myeloma, chronic lymphocytic leukaemia and lymphoplasmocytic lymphoma in 18, 13, 5 and 2 patients, respectively. IgM CG was associated with MGUS and Waldenström macroglobulinaemia in 8 and 18 cases, respectively. One third of patients did not receive any specific treatment. Various treatments, including rituximab, were administered to 25/31 patients with IgG CG and 6/25 patients with IgM CG due to CG-related symptoms. Rituximab was ineffective in all cases associated with a predominantly plasmacytic proliferation. To conclude, type I CG has specific clinico-biological characteristics compared to type II CG. Furthermore, there are differences in terms of related manifestations between type I IgG and type I IgM CG.Entities:
Keywords: cryoglobulinaemia; monoclonal gammopathy
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Year: 2014 PMID: 25363150 DOI: 10.1111/bjh.13196
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998