Cryofibrinogenemia

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Revision as of 19:36, 20 July 2020 by Aidan (talk | contribs) (Text replacement - "Clinical Presentation" to "Clinical Manifestations")

Definition

  • Disease caused by cold-precipitating proteins present in the plasma but not serum (i.e. associated with the clotting factors) that is associated with skin manifestations and thrombosis

Etiology

  • Primary
    • About half eventually develop lymphoma
  • Secondary
    • Cancer, usually lymphoma
    • Infection
      • Bacterial
      • Viral, including HIV, herpesviruses, and hepatitides
    • Autoimmune
      • Systemic lupus erythematosus
      • Sjögren syndrome
      • Rheumatoid arthritis
      • mixed CTD
      • Polymyositis
      • Dermatomyositis
      • Systemic sclerosis
      • Antiphospholipid syndrome
      • Hashimoto and Graves diseases
      • Sarcoidosis
      • Pyoderma gangrenosum
      • Psoriasis
      • Spondyloarthropathy
      • Inflammatory bowel disease
    • Vasculitis
      • ANCA-associated vasculitides
      • Giant cell arteritis
      • Behçet disease
      • Polyarteritis nodosa
      • Henoch-Schönlein purpura
    • Cryoglobulinemia

Pathophysiology

  • Cryofibrinogen is composed of fibrinogen, fibronectin, and fibrin, with or without albumin and immunoglobulins

Clinical Manifestations

  • Cold intolerance
  • Skin findings
    • Raynaud phenomenon
    • Purpura
    • Livedo reticularis
    • Skin necrosis
    • Acral ulcers
    • Gangrene
  • Arterial and venous thromboses

Investigations

  • Cryofibrinogen, returns as a percentage
    • Detectable in up to 7% of healthy patients

Management

  • Mild
    • Cold avoidance
  • Moderate
    • Corticosteroids
    • Aspirin
    • Alternatively, stanozolol 2 to 4mg BID (an anabolic steroid)
  • Severe
    • Plasmapheresis
    • Immunosupressing medications
      • Azathrioprine
      • Chlorambucil (in addition to corticosteroids)