Granulomatous allergic angiitis

From WikiMD's Food, Medicine & Wellness Encyclopedia

Granulomatous Allergic Angiitis, also known as Churg-Strauss Syndrome or Eosinophilic Granulomatosis with Polyangiitis (EGPA), is a rare autoimmune condition characterized by inflammation of the blood vessels (vasculitis) and the presence of granulomas (small areas of inflammation) within the affected tissues. This disease is part of a larger group of diseases known as Vasculitis which affects various organ systems including the lungs, skin, nervous system, and kidneys. The exact cause of Granulomatous Allergic Angiitis remains unknown, but it is believed to be an autoimmune disorder where the body's immune system mistakenly attacks healthy tissue.

Symptoms[edit | edit source]

The symptoms of Granulomatous Allergic Angiitis can vary widely depending on the organs affected but generally include asthma, sinusitis, skin rashes, fatigue, weight loss, and fever. More severe symptoms can involve the heart, kidneys, and nervous system leading to potentially life-threatening complications.

Diagnosis[edit | edit source]

Diagnosis of Granulomatous Allergic Angiitis involves a combination of clinical evaluation, laboratory tests including blood tests for eosinophils, and imaging studies. A definitive diagnosis often requires a biopsy of affected tissue to identify the characteristic granulomas and vasculitis.

Treatment[edit | edit source]

Treatment for Granulomatous Allergic Angiitis typically involves corticosteroids to reduce inflammation and suppress the immune system. In more severe cases, other immunosuppressive drugs may be used. The goal of treatment is to achieve remission and prevent relapse of the disease.

Epidemiology[edit | edit source]

Granulomatous Allergic Angiitis is a rare condition, with an estimated incidence of approximately 1-3 cases per million people per year. It can affect individuals of any age but is most commonly diagnosed in adults between the ages of 30 and 50.

Prognosis[edit | edit source]

The prognosis for individuals with Granulomatous Allergic Angiitis has improved significantly with the advent of effective treatment strategies. Early diagnosis and treatment are crucial in preventing irreversible organ damage and improving the quality of life for affected individuals.

Granulomatous allergic angiitis Resources
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Contributors: Prab R. Tumpati, MD