| Literature DB >> 29991541 |
Sariya Wongsaengsak1, Magdalena Czader2, Attaya Suvannasankha1,3.
Abstract
Cold agglutinin-mediated autoimmune haemolytic anaemia is associated with the development of autoantibodies that can agglutinate red blood cells at cold temperatures. While primary cold agglutinin disease is an idiopathic lymphoproliferative disorder, secondary cold agglutinin syndrome (CAS) complicates other diseases such as infections, autoimmune diseases and cancers, mostly low-grade lymphomas. Early recognition, treatment of CAS and treatment of its associated underlying diseases are crucial to a successful outcome. We report a case of CAS in a setting of diffuse large B cell lymphoma, in which the treatment course was complicated by worsened anaemia due to chemotherapy-induced myelosuppression. We reviewed previously reported cases and discussed diagnosis and treatment strategies, including novel complement inhibitors, as potential future therapy. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: haematology (drugs and medicines); malignant and benign haematology; malignant disease and immunosuppression
Mesh:
Year: 2018 PMID: 29991541 PMCID: PMC6047696 DOI: 10.1136/bcr-2017-222064
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X