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Raynaud's phenomenon - Management
Underlying causes of, or diseases associated with, secondary Raynaud's phenomenon

  • Connective tissue diseases:
    • Systemic sclerosis/scleroderma.
      • This includes CREST (Calcinosis, Raynaud's phenomenon, Esophageal dysfunction, Sclerodactyly, and Telangiectasia) syndrome, which is now more usually termed 'limited cutaneous systemic sclerosis'.
    • Systemic lupus erythematosus.
    • Rheumatoid arthritis.
    • Sjogren's syndrome.
    • Vasculitis (giant cell arteritis, Takayasu's arteritis, malnutrition).
    • Mixed or undifferentiated connective-tissue disease.
    • Dermatomyositis and polymyositis.
  • Vascular occlusive diseases:
    • Buerger's disease (thromboangiitis obliterans).
    • Arteriosclerosis.
    • Thromboembolic disease.
  • Drugs:
    • Amphetamines and cocaine.
    • Beta-blockers.
    • Angiotensin-converting enzyme (ACE) inhibitors.
    • Cancer chemotherapy (bleomycin, cisplatin, and vinblastine).
    • Ciclosporin.
    • Ergots/ergot derivatives (ergotamine, methysergide, bromocriptine, cabergoline, pergolide).
    • Interferon alpha and beta.
    • Combined oral contraceptives.
    • Sumatriptan.
    • Clonidine.
  • Haematological:
    • Polycythaemia.
    • Monoclonal gammopathies.
    • Paraproteinaemia.
    • Leukaemia.
    • Cryoglobulinaemia.
    • Cold agglutinin disease.
    • Protein C, protein S, or antithrombin III deficiency.
    • Factor V Leiden.
  • Occupational/environmental:
    • Vibration injury leading to vibration white finger (now referred to as 'hand–arm vibration syndrome').
    • Exposure to vinyl polychloride.
    • Frostbite/cold injury.
    • Ulnar aneurysm (hypothenar hammer syndrome).
  • Anatomical:
    • Thoracic outlet syndrome (caused by compression from a cervical rib or scalenus anterior muscle).
    • Carpal tunnel syndrome.
  • Infectious:
    • Hepatitis B and C (associated with cryoglobulinaemia).
    • Mycoplasma infections (cold agglutinins).
    • Parvovirus B19.
  • Endocrine:
    • Hypothyroidism.
    • Phaechromocytoma.
    • Carcinoid syndrome.

[Klippel, 2003; Gayraud, 2007; Pope, 2007b; Bakst et al, 2008]

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