Secondary amyloidosis risk factors: Difference between revisions

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** Inflammatory Arthritis
** Inflammatory Arthritis
** Adult-onset Still disease
** Adult-onset Still disease
** Ankylosing spondylitis
**[[Ankylosing spondylitis]]
** Juvenile idiopathic arthritis
**[[Juvenile idiopathic arthritis]]
** Psoriatic arthropathy
**[[Psoriatic arthropathy]]
** Reiter syndrome
**[[Reiter's syndrome|Reiter syndrome]]
** Rheumatoid arthritis
**[[Rheumatoid arthritis]]
** Gout
** Gout
** Systemic Vasculitis
** Systemic [[Vasculitis]]
** Antineutrophil cytoplasmic antibody-associated vasculitis
** Antineutrophil cytoplasmic antibody-associated vasculitis
** Behcet disease
**[[Behcet disease]]
** Giant cell arteritis
**[[Giant cell arteritis]]
** Polyarteritis nodosa
**[[Polyarteritis nodosa]]
** Polymyalgia rheumatica
**[[Polymyalgia rheumatica]]
** Systemic lupus erythematosus
**[[Systemic lupus erythematosus]]
** Takayasu arteritis
**[[Takayasu arteritis]]
** Inflammatory Bowel Disease
**[[Inflammatory Bowel Disease]]
** Ulcerative colitis
**[[Ulcerative colitis]]
** Crohn diseases
**[[Crohn disease]]
* Others include:
* Others include:
** Atrial myxoma
**[[Atrial myxoma]]
** Inflammatory abdominal aortic aneurism
** Inflammatory abdominal aortic aneurism
** Retroperitoneal fibrosis
**[[Retroperitoneal fibrosis]]
** SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome
** SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome
** Sarcoidosis
**[[Sarcoidosis]]
** Sinus histiocytosis with massive lymphadenopathy
** Sinus histiocytosis with massive lymphadenopathy
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 12:26, 30 October 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]

Overview

The most potent risk factor in the development of secondary amyloidosis is a persistent inflammatory disorders.

Risk Factors

References

  1. Koivuniemi, Riitta; Paimela, Leena; Suomalainen, Risto; Törnroth, Tom; Leirisalo-Repo, Marjatta (2009). "Amyloidosis is frequently undetected in patients with rheumatoid arthritis". Amyloid. 15 (4): 262–268. doi:10.1080/13506120802524676. ISSN 1350-6129.
  2. Blank, Norbert; Hegenbart, Ute; Dietrich, Sascha; Brune, Maik; Beimler, Jörg; Röcken, Christoph; Müller-Tidow, Carsten; Lorenz, Hanns-Martin; Schönland, Stefan O. (2018). "Obesity is a significant susceptibility factor for idiopathic AA amyloidosis". Amyloid. 25 (1): 37–45. doi:10.1080/13506129.2018.1429391. ISSN 1350-6129.
  3. van der Hilst, J. C. H.; Yamada, T.; Op den Camp, H. J. M.; van der Meer, J. W. M.; Drenth, J. P. H.; Simon, A. (2008). "Increased susceptibility of serum amyloid A 1.1 to degradation by MMP-1: potential explanation for higher risk of type AA amyloidosis". Rheumatology. 47 (11): 1651–1654. doi:10.1093/rheumatology/ken371. ISSN 1462-0324.
  4. Papa, Riccardo; Doglio, Matteo; Lachmann, Helen J.; Ozen, Seza; Frenkel, Joost; Simon, Anna; Neven, Bénédicte; Kuemmerle-Deschner, Jasmin; Ozgodan, Huri; Caorsi, Roberta; Federici, Silvia; Finetti, Martina; Trachana, Maria; Brunner, Jurgen; Bezrodnik, Liliana; Pinedo Gago, Mari Carmen; Maggio, Maria Cristina; Tsitsami, Elena; Al Suwairi, Wafaa; Espada, Graciela; Shcherbina, Anna; Aksu, Guzide; Ruperto, Nicolino; Martini, Alberto; Ceccherini, Isabella; Gattorno, Marco (2017). "A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry". Orphanet Journal of Rare Diseases. 12 (1). doi:10.1186/s13023-017-0720-3. ISSN 1750-1172.