Share these talks and lectures with your colleagues
Invite colleaguesWe noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at support@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support support@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support support@hstalks.com
We hope you have enjoyed this limited-length demo talk
This is a limited length demo talk; you may
login
or review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Objectives
- Idiopathic inflammatory myopathies
- Clinical presentation
- Bohan and Peter criteria
- Advances
- Dermatomyositis and polymyositis
- Idiopathic inflammatory myopathies
- Dermatomyositis
- Dermatomyositis rashes
- Pattern of weakness: dermatomyositis
- Polymyositis
- Inclusion body myositis (IBM)
- Patterns of weakness: IBM
- Asymmetric forearm scooping
- Immune-mediated necrotizing myopathy
- Summary of the different sub-groups
- Evaluation
- Strength testing
- Skin exam
- Assessment for other organ involvement
- Myositis specific antibodies
- Dermatomyositis specific antibodies (1)
- Dermatomyositis specific antibodies (2)
- IMNM specific antibodies
- IBM- related antibody
- Myositis associated antibodies
- Myositis antibodies and clinical associations
- EMG
- MRI
- Muscle biopsy
- Pathology: Dermatomyositis
- Pathology: Polymyositis
- Pathology: IBM
- Pathology: IMNM
- Considerations for treatment
- Treatment options
- Challenges
- Conclusions
Topics Covered
- Clinical presentation of the idiopathic inflammatory myopathies
- Classification criteria for myositis
- Myositis antibodies and clinical associations
- Diagnostic tools and evaluation of myositis
- Treatment strategies for myositis
Links
Categories:
Therapeutic Areas:
Talk Citation
Albayda, J. (2017, January 30). An overview of the idiopathic inflammatory myopathies [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved February 23, 2019, from https://hstalks.com/bs/3428/.Publication History
An overview of the idiopathic inflammatory myopathies
Published on January 30, 2017
36 min
Other Talks in the Therapeutic Area: Immunology & Inflammation
Transcript
0:00
My name is Jemima Albayda.
I'm an Assistant Professor
at the Johns Hopkins University,
seeing patients
at the Division of Rheumatology,
Myositis Center.
Today, I will give you "An overview
of the Idiopathic
Inflammatory Myopathies".
0:17
Our objectives with this talk
are to describe
the clinical presentation
of the idiopathic
inflammatory myopathies.
To define
the subgroups of myositis.
And present the framework
for current understanding
of classification.
To enumerate
the known antibody associations.
And discuss how they help guide
prognosis and management.
To detail the clinical evaluation
of myositis
and the role of ancillary testing.
And to briefly discuss
treatment strategies.
0:47
The idiopathic
inflammatory myopathies
are a rare group of acquired
autoimmune muscle disorders.
Clinically, they are characterized
by muscle weakness
and by inflammatory cell
infiltrates in the muscle.
Although, it is thought
of as a muscle disorder,
it is quite heterogenous
in presentation
and treatment response.
Extramuscular manifestations
are often seen
and can include skin
and lung inflammation,
joint, heart,
and rarely GI tract involvement.
There's also a known increased risk
of malignancy,
particularly,
in cases of dermatomyositis.