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Systemic Amyloidosis due to Low-Grade Lymphoma

Wechalekar, AD; Chakraborty, R; Lentzsch, S; (2020) Systemic Amyloidosis due to Low-Grade Lymphoma. Hematology/Oncology Clinics of North America , 34 (6) pp. 1027-1039. 10.1016/j.hoc.2020.08.016. Green open access

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Abstract

Lymphoma-related amyloidosis is a rare entity. Systemic AL amyloidosis is generally caused by an underlying plasma cell clone in the bone marrow with an intact monoclonal immunoglobulin G (IgG) or IgA protein. The rarity of the lymphoma-related amyloidosis makes the generation of data in randomized trials and the determination of the optimal treatment almost impossible. Therefore, treatment recommendations discussed here are based on either retrospective or small prospective trials of single centers.

Type: Article
Title: Systemic Amyloidosis due to Low-Grade Lymphoma
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.hoc.2020.08.016
Publisher version: https://doi.org/10.1016/j.hoc.2020.08.016
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.
Keywords: IgM amyloidosis, Lymphoma-related AL amyloidosis, Rituximab, Waldenstrom macroglobulinemia
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine > Inflammation
URI: https://discovery.ucl.ac.uk/id/eprint/10114979
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