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Printable Handouts
Navigable Slide Index
- Introduction
- Goals
- Review
- SSc pathogenesis
- Organ complications associated with SSc
- Sclerodactyly
- Raynaud’s phenomenon
- Calcinosis
- Dilated nailfold capillaries
- Telangiectasias
- Esophageal dysmotility
- Interstitial lung disease (ILD)
- Classification
- Classification of diffused and limited cutaneous SSc
- Classification criteria for scleroderma
- Autoantibodies
- Screening: early identification
- Screening and monitoring
- Pulmonary arterial hypertension (PAH)
- PAH management
- PAH therapy
- SSc-ILD overview
- SSc-ILD: predictors of progression and management
- SSc-ILD: therapy
- Scleroderma renal crisis (SRC)
- SRC management and outcomes
- Renal biopsy findings in SRC
- Raynaud’s and digital ulcers
- Pathophysiology of vascular changes in SSc
- Raynaud’s therapy
- Skin fibrosis
- Histopathology of scleroderma in skin
- Therapy for skin fibrosis
- Gastrointestinal involvement in SSc
- Gastric antral vascular ectasia (GAVE): watermelon stomach
- Gastroesophageal reflux disease (GERD)
- Bacterial overgrowth (SIBO)
- Cardiac involvement in SSc
- Symptom-directed adjuvant treatment options for SSc
- Financial disclosure
Topics Covered
- Systemic sclerosis pathogenesis
- Scleroderma
- Raynaud’s phenomenon
- Calcinosis
- Dilated nailfold capillaries
- Telangiectasias
- Interstitial lung disease
- SSc classification
- Pulmonary arterial hypertension
- SSc renal crisis
- Gastrointestinal involvement in SSc
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Derk, C. (2026, May 28). Systemic sclerosis (SSc) [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved May 29, 2026, from https://doi.org/10.69645/BSYI7444.Export Citation (RIS)
Publication History
- Published on May 28, 2026
Financial Disclosures
- PI on Glaxo Smith Kline research study.
A selection of talks on Physiology & Anatomy
Transcript
Please wait while the transcript is being prepared...
0:00
My name is Chris Derk.
I'm a Professor of
Clinical Medicine at
the Division of Rheumatology
at the University
of Pennsylvania.
This talk is in regards
to systemic sclerosis.
0:12
The goals of this
talk will be to
discuss the overview
of the disease.
Discuss a little bit about
basic pathophysiology
and the clinical
manifestations of the disease.
Discuss a little bit
about classification,
screening when somebody sees
the patient in the clinic
and then on follow-up,
and then some up-to-date
organ-specific
management that is
current at the time.
0:38
To start out, I'm going to talk
about the pathophysiology
of the disease.
This is an autoimmune
connective tissue disease of
unknown etiology, which is
characterized by the
triad of fibrosis,
vascular dysfunction, and
immune dysregulation.
The theory is that
in patients who have
a permissive genetic background
some etiologic agent, such
as an environmental factor
such as a virus or a
chemical agent triggers
a change at the molecular
and cellular level.
The initial event
is thought to be
at the endothelial
cell wall level,
and this leads to inflammation
and changes of the vessel wall.
Transmigration of cells from
the vessel into the
surrounding tissue
and inflammatory infiltrate,
production of certain cytokines
and growth factors
that then leads
to an increased production of
collagen in both the skin,
as well as other
visceral organs.
Then production of
auto antibodies, which
at this point are not thought
to be directly pathogenic.
Again, with this graph here,