Polymyositis and dermatomyositis classification: Difference between revisions
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==Overview== | ==Overview== | ||
Polymyositis and dermatomyositis | Polymyositis and dermatomyositis is one of the subtypes of idiopathic [[inflammatory myopathy]]. The 2017 European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) classified idiopathic [[inflammatory myopathy]] into 6 subtypes including polymyositis, dermatomyositis, inclusion body myositis, immune-mediated necrotizing myopathies (IMNM), amyopathic dermatomyositis, and juvenile dermatomyositis. | ||
==Classification== | ==Classification== | ||
*Polymyositis and dermatomyositis is one of the subtypes of inflammatory | *Polymyositis and dermatomyositis is one of the subtypes of idiopathic [[inflammatory myopathy]].<ref>Bronner, I. M. (2009). Polymyositis and dermatomyositis: classification, risk factors and outcome (Doctoral dissertation, Universiteit van Amsterdam [Host]).</ref><ref name="Hilton-Jones2011">{{cite journal|last1=Hilton-Jones|first1=David|title=Observations on the classification of the inflammatory myopathies|journal=La Presse Médicale|volume=40|issue=4|year=2011|pages=e199–e208|issn=07554982|doi=10.1016/j.lpm.2010.10.035}}</ref> | ||
* | *The 2017 European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) classified idiopathic [[inflammatory myopathy]] into 6 subtypes:<ref name="pmid29550929">{{cite journal |vauthors=Leclair V, Lundberg IE |title=New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter |journal=Curr Rheumatol Rep |volume=20 |issue=4 |pages=18 |date=March 2018 |pmid=29550929 |pmc=5857275 |doi=10.1007/s11926-018-0726-4 |url=}}</ref><ref name="pmid29079590">{{cite journal |vauthors=Lundberg IE, Tjärnlund A, Bottai M, Werth VP, Pilkington C, Visser M, Alfredsson L, Amato AA, Barohn RJ, Liang MH, Singh JA, Aggarwal R, Arnardottir S, Chinoy H, Cooper RG, Dankó K, Dimachkie MM, Feldman BM, Torre IG, Gordon P, Hayashi T, Katz JD, Kohsaka H, Lachenbruch PA, Lang BA, Li Y, Oddis CV, Olesinska M, Reed AM, Rutkowska-Sak L, Sanner H, Selva-O'Callaghan A, Song YW, Vencovsky J, Ytterberg SR, Miller FW, Rider LG |title=2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups |journal=Ann. Rheum. Dis. |volume=76 |issue=12 |pages=1955–1964 |date=December 2017 |pmid=29079590 |doi=10.1136/annrheumdis-2017-211468 |url=}}</ref><ref name="BenvenisteLéger2011">{{cite journal|last1=Benveniste|first1=Olivier|last2=Léger|first2=Jean-Marc|title=Inflammatory or necrotizing myopathies, myositides and other acquired myopathies, new insight in 2011|journal=La Presse Médicale|volume=40|issue=4|year=2011|pages=e197–e198|issn=07554982|doi=10.1016/j.lpm.2011.02.002}}</ref> | ||
** | **Polymyositis | ||
**Dermatomyositis | |||
**[[Inclusion body myositis]] | |||
**Immune-mediated necrotizing myopathies (IMNM) | |||
**Amyopathic dermatomyositis | |||
**Juvenile dermatomyositis | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Medicine]] | |||
[[Category:Rheumatology]] | |||
[[Category:Dermatology]] | |||
[[Category:Up-To-Date]] | |||
Latest revision as of 23:47, 29 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]
Overview
Polymyositis and dermatomyositis is one of the subtypes of idiopathic inflammatory myopathy. The 2017 European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) classified idiopathic inflammatory myopathy into 6 subtypes including polymyositis, dermatomyositis, inclusion body myositis, immune-mediated necrotizing myopathies (IMNM), amyopathic dermatomyositis, and juvenile dermatomyositis.
Classification
- Polymyositis and dermatomyositis is one of the subtypes of idiopathic inflammatory myopathy.[1][2]
- The 2017 European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) classified idiopathic inflammatory myopathy into 6 subtypes:[3][4][5]
- Polymyositis
- Dermatomyositis
- Inclusion body myositis
- Immune-mediated necrotizing myopathies (IMNM)
- Amyopathic dermatomyositis
- Juvenile dermatomyositis
References
- ↑ Bronner, I. M. (2009). Polymyositis and dermatomyositis: classification, risk factors and outcome (Doctoral dissertation, Universiteit van Amsterdam [Host]).
- ↑ Hilton-Jones, David (2011). "Observations on the classification of the inflammatory myopathies". La Presse Médicale. 40 (4): e199–e208. doi:10.1016/j.lpm.2010.10.035. ISSN 0755-4982.
- ↑ Leclair V, Lundberg IE (March 2018). "New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter". Curr Rheumatol Rep. 20 (4): 18. doi:10.1007/s11926-018-0726-4. PMC 5857275. PMID 29550929.
- ↑ Lundberg IE, Tjärnlund A, Bottai M, Werth VP, Pilkington C, Visser M, Alfredsson L, Amato AA, Barohn RJ, Liang MH, Singh JA, Aggarwal R, Arnardottir S, Chinoy H, Cooper RG, Dankó K, Dimachkie MM, Feldman BM, Torre IG, Gordon P, Hayashi T, Katz JD, Kohsaka H, Lachenbruch PA, Lang BA, Li Y, Oddis CV, Olesinska M, Reed AM, Rutkowska-Sak L, Sanner H, Selva-O'Callaghan A, Song YW, Vencovsky J, Ytterberg SR, Miller FW, Rider LG (December 2017). "2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups". Ann. Rheum. Dis. 76 (12): 1955–1964. doi:10.1136/annrheumdis-2017-211468. PMID 29079590.
- ↑ Benveniste, Olivier; Léger, Jean-Marc (2011). "Inflammatory or necrotizing myopathies, myositides and other acquired myopathies, new insight in 2011". La Presse Médicale. 40 (4): e197–e198. doi:10.1016/j.lpm.2011.02.002. ISSN 0755-4982.