'Transformation' from amyloid light chain amyloidosis to symptomatic multiple myeloma

Publication date

2018-07

Authors

Rutten, Karlijn H G
Raijmakers, ReinierISNI 0000000390368177
Minnema, Monique C.ORCID 0000-0002-3139-8379ISNI 0000000394782842

Editors

Advisors

Supervisors

DOI

Document Type

Article

Collections

Open Access logo

License

taverne

Abstract

Amyloid light chain (AL) amyloidosis and multiple myeloma (MM) are both clonal plasma cell disorders, and may be concurrently present in patients. However, symptomatic MM seldom develops in patients with AL amyloidosis, while the other way around is common. With this case report, we discuss the difficulties in the differential diagnosis between AL amyloidosis and MM, and extend on the possible mechanisms involved in the development of these overlapping disorders. In addition, we provide clinicians with tools that may help improve their management and monitoring of such patients.

Keywords

Amyloidosis, Multiple myeloma, Plasma cell dyscrasia, Taverne, Internal Medicine

Citation

Rutten, K H G, Raymakers, R A P & Minnema, M C 2018, ''Transformation' from amyloid light chain amyloidosis to symptomatic multiple myeloma', Netherlands Journal of Medicine, vol. 76, no. 5, pp. 249-250.