Two distinct syndromes of lymphoma associated AL amyloidosis: A case series and review of the literature

Light chain (AL) amyloidosis has a rare association with non-Hodgkin lymphoma (NHL). Both peritumoral and systemic AL amyloidosis have been reported, but a detailed description of these syndromes is lacking. We describe 10 patients with lymphoma associated AL amyloidosis. NHL patients with peritumor...

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Bibliographic Details
Published in:American journal of hematology Vol. 85; no. 10; pp. 805 - 808
Main Authors: Telio, David, Bailey, Denis, Chen, Christine, Crump, Michael, Reece, Donna, Kukreti, Vishal
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-10-2010
Wiley-Liss
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Summary:Light chain (AL) amyloidosis has a rare association with non-Hodgkin lymphoma (NHL). Both peritumoral and systemic AL amyloidosis have been reported, but a detailed description of these syndromes is lacking. We describe 10 patients with lymphoma associated AL amyloidosis. NHL patients with peritumoral amyloidosis had low or undetectable levels of monoclonal (M) protein, mostly single organ involvement(lung or soft tissue), and underlying extranodal marginal zone lymphoma, mucosa associated lymphoid tissue subtype. NHL patients with systemic amyloidosis had high levels of M-protein, multiorgan involvement with frequent cardiac involvement, and predominantly underlying lymphoplasmacytic lymphoma. Systemic amyloidosis was associated with inferior outcomes
Bibliography:Conflict of interest: Nothing to report.
SourceType-Scholarly Journals-1
ObjectType-Correspondence-1
ObjectType-Feature-4
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ObjectType-Review-2
ObjectType-Article-3
ISSN:0361-8609
1096-8652
DOI:10.1002/ajh.21814