Eosinophilic vasculitis
| Eosinophilic vasculitis | |
|---|---|
| Synonyms | |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Fever, fatigue, weight loss, skin rash, muscle pain, joint pain |
| Complications | Organ damage, neuropathy, kidney failure |
| Onset | |
| Duration | |
| Types | |
| Causes | Autoimmune disorder |
| Risks | |
| Diagnosis | Blood test, biopsy, imaging studies |
| Differential diagnosis | Churg-Strauss syndrome, Polyarteritis nodosa, Microscopic polyangiitis |
| Prevention | |
| Treatment | Corticosteroids, immunosuppressive drugs |
| Medication | Prednisone, Cyclophosphamide, Methotrexate |
| Prognosis | |
| Frequency | |
| Deaths | |
Eosinophilic vasculitis is a rare type of vasculitis that is characterized by the presence of eosinophils in the blood vessels. This condition can affect various organs in the body, including the skin, lungs, and gastrointestinal tract.
Symptoms[edit | edit source]
The symptoms of eosinophilic vasculitis can vary depending on the organs affected. Common symptoms include:
Causes[edit | edit source]
The exact cause of eosinophilic vasculitis is unknown. However, it is believed to be an autoimmune disease, where the body's immune system mistakenly attacks its own tissues.
Diagnosis[edit | edit source]
Diagnosis of eosinophilic vasculitis is often challenging due to its rarity and the wide range of symptoms. It typically involves a combination of blood tests, imaging studies, and sometimes a biopsy of affected tissue.
Treatment[edit | edit source]
Treatment for eosinophilic vasculitis typically involves medications to reduce inflammation and suppress the immune system. These may include corticosteroids and immunosuppressive drugs.
See also[edit | edit source]
References[edit | edit source]
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