Systemic Sclerosis Flashcards
1
Q
What is SS?
A
- Autoimmune inflammatory and fibrotic connective tissue disease
2
Q
What are the two types of SS?
A
- Limited Cutaneous Systemic Sclerosis (more common)
- Skin affected: face, forearms, lower legs up to knee
- Diffuse Cutaneous Systemic Sclerosis
- Skin affected: upper arms, thighs, trunk
3
Q
What are the features of LcSSc?
*remember CREST syndrome
A
- Calcinosis
- Raynaud’s disease
- Esophageal dysmotility
- Sclerodactyly
- Telangiectasia
4
Q
A
5
Q
What are the features of DC
cSSc?
A
- CREST + Internal organs
- CVS: HTN, CAD
- Lungs: Pulmonary HTN & Pulmonary Fibrosis
- Kidneys: Glomerulonephritis, scleroderma renal crisis
6
Q
What are the cardinal features of SSc
A
- Excessive collagen production and deposition
- Vascular damage
- Immune system activation via autoantibody production and cell-mediated autoimmune mechanism
7
Q
What are the features of SSc?
A
- Scleroderma - hardening of skin
- Sclerodactyly - skin tightening around joints
- Telangiectasia
- Calcinosis
- Raynaud’s phenomenon
- Oesophageal dysmotility
- Systemic and pulmonary HTN
- Pulmonary Fibrosis
- Scleroderma renal crisis
- Myalgia, joint pain
*basically all systems are affected. Refer patientinfo for full list
8
Q
What Ix would you order for SSc?
A
- Bloods
- FBC
- ESR
- CRP
- U&E
- Autoantibodies
- ANA - sensitive but not specific
- Specific
- Anti-centromere antibodies - LcSSc
- scl-70 antibodies - DcSSc
- Nailfold capillaroscopy
9
Q
A
10
Q
What features will you find in nailfold capillaroscopy?
A
- Abnormal capillaries
- Avascular areas
- Micro haemorrhages
11
Q
What are the diagnostic crietria for SSc?
*must be equal to or > 9
A
- Skin thickening extending proximal to the MCP joints (score 9).
- Skin thickening of the fingers (score 2 for puffy fingers, 4 for sclerodactyly).
- Fingertip lesions (score 2 for ulcers, 3 for fingertip pitting scars).
- Telangiectasia (score 2).
- Abnormal nailfold capillaries (score 2).
- Pulmonary arterial hypertension and/or interstitial lung disease (score 2).
- Raynaud’s phenomenon (score 3).
- SSc-related autoantibodies (score 3
12
Q
What are the differential diagnosis for SSc?
A
- Raynaud’s phenomenon from other causes
- Vibration injury
- RA or SLE
- Amyloidosis
- Chronic graft vs host disease
- Paraneoplastic syndrome
13
Q
How would you mx SSc non-pharmalogically?
A
- Avoid smoking
- Gentle skin stretching to maintain the range of motion
- Regular emollients
- Avoiding cold triggers for Raynaud’s
- Physiotherapy to maintain healthy joints
- Occupational therapy for adaptations to daily living to cope with limitations
14
Q
How would you mx SSc medically?
A
*no standardised tx for SSc yet.
- Nifedipine - Raynaud’s phenomenon
- Anti acid medications (e.g. PPIs) and pro-motility medications (e.g. metoclopramide) for gastrointestinal symptoms
- Analgesia - joint pain
- Antibiotics - skin infections
- Antihypertensives can be used to treat hypertension (usually ACE inhibitors)
- Treatment of pulmonary artery hypertension
- Supportive management of pulmonary fibrosis