Autoimmune vasculitis

From WikiMD's Wellness Encyclopedia

Autoimmune Vasculitis Autoimmune vasculitis is a group of disorders characterized by inflammation of blood vessels due to an autoimmune response. This condition can affect various organs and tissues, leading to a wide range of symptoms and complications.

Overview[edit | edit source]

Autoimmune vasculitis occurs when the body's immune system mistakenly attacks its own blood vessels, causing inflammation and damage. This can lead to narrowing or blockage of the vessels, reducing blood flow to vital organs and tissues.

Types of Autoimmune Vasculitis[edit | edit source]

There are several types of autoimmune vasculitis, each affecting different sizes and types of blood vessels:

Symptoms[edit | edit source]

Symptoms of autoimmune vasculitis vary depending on the type and organs involved, but common symptoms include:

  • Fever
  • Fatigue
  • Weight loss
  • Muscle and joint pain
  • Skin rashes
  • Neurological symptoms

Diagnosis[edit | edit source]

Diagnosing autoimmune vasculitis involves a combination of clinical evaluation, laboratory tests, and imaging studies. Common diagnostic tools include:

  • Blood tests for inflammatory markers and specific antibodies
  • Urinalysis to check for kidney involvement
  • Imaging studies such as CT or MRI scans
  • Biopsy of affected tissue

Treatment[edit | edit source]

Treatment of autoimmune vasculitis aims to reduce inflammation and suppress the immune system. Common treatments include:

  • Corticosteroids to reduce inflammation
  • Immunosuppressive drugs such as cyclophosphamide or methotrexate
  • Biologic agents targeting specific immune pathways

Prognosis[edit | edit source]

The prognosis for autoimmune vasculitis varies depending on the type and severity of the disease. Early diagnosis and treatment are crucial for improving outcomes and preventing organ damage.

See Also[edit | edit source]

External Links[edit | edit source]

NIH genetic and rare disease info[edit source]

Autoimmune vasculitis is a rare disease.

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Contributors: Prab R. Tumpati, MD