Vasculitis is a group of autoimmune disorders that cause inflammation of blood vessels, which can reduce blood flow and damage vital organs. The condition varies depending on the size and location of the affected vessels.
Common types include giant cell arteritis (GCA), granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and polyarteritis nodosa (PAN).
Because vasculitis can affect many different organs, symptoms vary significantly. Common signs may include:
Urgent evaluation is essential when symptoms suggest possible eye, kidney, or organ involvement, as these can progress rapidly without treatment.
Diagnosis requires a combination of lab testing, imaging, and, in some cases, a tissue biopsy to confirm inflammation and assess severity. Tests may include:
Treatment depends on the type and severity of vasculitis, but always focuses on controlling inflammation and preventing organ damage. Management may include:
With early diagnosis and expert management, many types of vasculitis can be brought into remission. Ongoing follow-up is vital to monitor for relapse, protect organ function, and maintain overall health. Most patients lead active, fulfilling lives with proper long-term care.