Granulomatous Polyangiitis Treatment

• January 12, 2024
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A rare autoimmune condition called granulomatosis with polyangiitis (GPA) damages vital organs and produces inflammation in blood vessels. Before, it was referred to as Wegener's granulomatosis. Anti-neutrophil cytoplasmic antibodies (ANCAs) are frequently linked to GPA, a systemic small and medium vessel vasculitis. The non-specificity and variability of symptoms can cause a delay in diagnosis. An unusual condition called granulomatosis with polyangiitis results in inflammation of the blood vessels in your kidneys, nose, sinuses, throat, and lungs. This ailment was formerly known as Wegener's granulomatosis and is a member of the vasculitis group of blood vessel disorders. Some of your organs' blood flow is slowed by it. Granulomas, which are regions of inflammation in the affected tissues, might impair the function of these organs. A full recovery from granulomatosis with polyangiitis may be possible with early diagnosis and treatment. The illness may not be curable without medical attention.

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