AA amyloidosis complicating monoclonal gammopathies, an unusual feature validating the concept of "monoclonal gammopathy of inflammatory significance"?. Issue 11 (21st September 2021)
- Record Type:
- Journal Article
- Title:
- AA amyloidosis complicating monoclonal gammopathies, an unusual feature validating the concept of "monoclonal gammopathy of inflammatory significance"?. Issue 11 (21st September 2021)
- Main Title:
- AA amyloidosis complicating monoclonal gammopathies, an unusual feature validating the concept of "monoclonal gammopathy of inflammatory significance"?
- Authors:
- Terré, Alexandre
Colombat, Magali
Cez, Alexandre
Martin, Claire
Diet, Carine
Brechignac, Sabine
Oghina, Silvia
Bodez, Diane
Faguer, Stanislas
Savey, Léa
Galland, Joris
Boffa, Jean‐Jacques
Grateau, Gilles
Jaccard, Arnaud
Buob, David
Georgin‐Lavialle, Sophie - Abstract:
- Abstract: Introduction: AL amyloidosis is caused by the proliferation of an immunoglobulin‐secreting B cell clone. AA amyloidosis is a rare complication of chronic inflammation. However, some patients present with diseases combining monoclonal immunoglobulin production and chronic inflammation. The aim of this work was to describe cases of AA amyloidosis associated with monoclonal gammopathies. Patients and methods: We reviewed all patients reported in French national amyloid centres presenting with AA amyloidosis and monoclonal gammopathy and performed a literature review. The quality of AA amyloidosis diagnosis and the causal relationship with monoclonal gammopathy were assessed. Results: In total, four patients from our centres and eight from the literature fulfilled the inclusion criteria. The haematological disorders presenting with monoclonal gammopathy were as follows: Waldenström macroglobulinaemia (n = 8), Schnitzler syndrome (n = 2), multiple myeloma (n = 1) and monoclonal gammopathy of undetermined significance (n = 1). Treatment strategies varied among the cases, with the treatment of the haematological disorder in 4 and anti‐inflammatory treatment in 2. Conclusion: Monoclonal gammopathies might be a rare and poorly known cause of AA amyloidosis. Such monoclonal gammopathies could be named "monoclonal gammopathies of inflammatory significance."
- Is Part Of:
- International journal of clinical practice. Volume 75:Issue 11(2021)
- Journal:
- International journal of clinical practice
- Issue:
- Volume 75:Issue 11(2021)
- Issue Display:
- Volume 75, Issue 11 (2021)
- Year:
- 2021
- Volume:
- 75
- Issue:
- 11
- Issue Sort Value:
- 2021-0075-0011-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-09-21
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Periodicals
610.5 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://www.blackwell-synergy.com/loi/ijcp ↗
http://www.blackwell-synergy.com/openurl?genre=journal&eissn=1742-1241 ↗
http://www.blackwellpublishing.com/journal.asp?ref=1368-5031&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1742-1241 ↗
https://www.hindawi.com/journals/ijclp/ ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ijcp.14817 ↗
- Languages:
- English
- ISSNs:
- 1368-5031
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.172160
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- 24518.xml