AA amyloidosis complicating monoclonal gammopathies, an unusual feature validating the concept of "monoclonal gammopathy of inflammatory significance"?


Journal

International journal of clinical practice
ISSN: 1742-1241
Titre abrégé: Int J Clin Pract
Pays: India
ID NLM: 9712381

Informations de publication

Date de publication:
Nov 2021
Historique:
revised: 23 07 2021
received: 24 02 2021
accepted: 03 09 2021
pubmed: 8 9 2021
medline: 27 10 2021
entrez: 7 9 2021
Statut: ppublish

Résumé

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. 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. 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. Monoclonal gammopathies might be a rare and poorly known cause of AA amyloidosis. Such monoclonal gammopathies could be named "monoclonal gammopathies of inflammatory significance."

Identifiants

pubmed: 34490695
doi: 10.1111/ijcp.14817
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14817

Informations de copyright

© 2021 John Wiley & Sons Ltd.

Références

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Auteurs

Alexandre Terré (A)

Department of Internal Medicine, Centre de référence des maladies auto-inflammatoires et des amyloses d'origine inflammatoire (CEREMAIA), Sorbonne University, AP-HP, Tenon Hospital, Paris, France.
Laboratoire d'Excellence GR-Ex, Institut Imagine, INSERM U1163, CNRS ERL 8254, Université Paris Descartes, Sorbonne Paris-Cité, Paris, France.

Magali Colombat (M)

Department of Pathology, CHU Toulouse, Toulouse, France.

Alexandre Cez (A)

Department of Nephrology, Sorbonne University, Tenon Hospital, Paris, France.

Claire Martin (C)

Rheumatology Department, La Rochelle Hospital, La Rochelle, France.

Carine Diet (C)

Nephrology Department, Henri Mondor Hospital, Creteil, France.

Sabine Brechignac (S)

Haematology Department, Avicenne Hospital, Bobigny, France.

Silvia Oghina (S)

Cardiology Department, Henri Mondor Hospital, National Reference Centre of Cardiac Amyloidosis, Creteil, France.

Diane Bodez (D)

Cardiology Department, Centre Cardiologique du Nord, Saint-Denis, France.

Stanislas Faguer (S)

Département de Néphrologie et Transplantation d'Organes, CHU de Toulouse, Toulouse, France.

Léa Savey (L)

Department of Internal Medicine, Centre de référence des maladies auto-inflammatoires et des amyloses d'origine inflammatoire (CEREMAIA), Sorbonne University, AP-HP, Tenon Hospital, Paris, France.

Joris Galland (J)

Department of Internal Medicine, Centre de référence des maladies auto-inflammatoires et des amyloses d'origine inflammatoire (CEREMAIA), Sorbonne University, AP-HP, Tenon Hospital, Paris, France.

Jean-Jacques Boffa (JJ)

Nephrology Department, Henri Mondor Hospital, Creteil, France.

Gilles Grateau (G)

Department of Internal Medicine, Centre de référence des maladies auto-inflammatoires et des amyloses d'origine inflammatoire (CEREMAIA), Sorbonne University, AP-HP, Tenon Hospital, Paris, France.
Inserm UMRS_933, et laboratoire de génétique, Faculté de médecine, Sorbonne University, Trousseau Hospital, AP-HP, Paris, France.

Arnaud Jaccard (A)

Haematology Department, CHU Dupuytren, National Reference Center for AL Amyloidosis Limoges, France.

David Buob (D)

Department of Pathology, Sorbonne University, Tenon Hospital, Paris, France.

Sophie Georgin-Lavialle (S)

Department of Internal Medicine, Centre de référence des maladies auto-inflammatoires et des amyloses d'origine inflammatoire (CEREMAIA), Sorbonne University, AP-HP, Tenon Hospital, Paris, France.
Inserm UMRS_933, et laboratoire de génétique, Faculté de médecine, Sorbonne University, Trousseau Hospital, AP-HP, Paris, France.

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