Systemic Sclerosis Flashcards

1
Q

What is SS?

A
  • Autoimmune inflammatory and fibrotic connective tissue disease
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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
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3
Q

What are the features of LcSSc?

*remember CREST syndrome

A
  • Calcinosis
  • Raynaud’s disease
  • Esophageal dysmotility
  • Sclerodactyly
  • Telangiectasia
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4
Q
A
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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
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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
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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

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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
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9
Q
A
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10
Q

What features will you find in nailfold capillaroscopy?

A
  • Abnormal capillaries
  • Avascular areas
  • Micro haemorrhages
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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
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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
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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
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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
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