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Health Conditions and ConcernsGlobal Rank
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Granulomatosis with polyangiitis - Symptoms and causes
WEBNov 30, 2022 · Granulomatosis with polyangiitis is an uncommon disorder that causes inflammation of the blood vessels in your nose, sinuses, throat, lungs and kidneys. Formerly called Wegener's granulomatosis, this condition is one of a group of blood vessel disorders called vasculitis. It slows blood flow to some of your organs.
Mayoclinic.orgGranulomatosis with polyangiitis - Wikipedia
WEBGranulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis (WG), [1] [2] [3] [4] [5] after the German physician Friedrich Wegener, is a rare long-term systemic disorder that involves the formation of granulomas and inflammation of blood vessels (vasculitis).
En.m.wikipedia.orgGranulomatosis with Polyangiitis (GPA, formerly called Wegener’s)
WEBJul 16, 2019 · Granulomatosis with polyangiitis (formerly called Wegener’s) is a rare disease of uncertain cause that can affect people of all ages. It is characterized by inflammation in various tissues, including blood vessels (vasculitis), but primarily parts of the respiratory tract and the kidneys.
My.clevelandclinic.orgGranulomatosis with polyangiitis - Diagnosis and treatment
WEBNov 30, 2022 · Diagnosis. Your doctor will ask you about your signs and symptoms, conduct a physical exam, and take your medical history. Lab tests. Blood tests can check for: Signs of inflammation, such as a high level of C-reactive protein or a high erythrocyte sedimentation rate — commonly referred to as a sed rate.
Mayoclinic.orgGranulomatosis with Polyangiitis - Johns Hopkins Vasculitis
WEBGranulomatosis with Polyangiitis is a disease involving granulomatous inflammation, necrosis and vasculitis that most frequently targets the upper respiratory tract, lower respiratory tract, and kidneys.
Hopkinsvasculitis.orgGranulomatosis with Polyangiitis | Johns Hopkins Medicine
WEBGranulomatosis with polyangiitis (GPA) is an autoimmune disorder that causes swelling and irritation in blood vessels and other tissues. It's uncommon. The exact cause is unknown. It's not hereditary or contagious. Most people with …
Hopkinsmedicine.orgGranulomatosis With Polyangiitis - StatPearls - NCBI Bookshelf
WEBAug 31, 2024 · Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis, is a necrotizing vasculitis affecting small to medium-sized vessels. GPA is part of a spectrum of disorders known as antineutrophil cytoplasmic antibody (ANCA)–associated vasculitides.
Ncbi.nlm.nih.govGranulomatosis with Polyangiitis (GPA) - Granulomatosis with
WEBPathophysiology |. Symptoms and Signs |. Diagnosis |. Prognosis |. Treatment |. Key Points. Granulomatosis with polyangiitis is characterized by necrotizing granulomatous inflammation, small- and medium-sized vessel vasculitis, and focal necrotizing glomerulonephritis, often with crescent formation.
Merckmanuals.comGranulomatosis with Polyangiitis (GPA, formerly Wegener
WEBAug 21, 2024 · Granulomatosis with polyangiitis (GPA), formerly known as Wegener granulomatosis, is a rare multisystem autoimmune disease of unknown etiology. GPA is one of the antineutrophil cytoplasmic
Emedicine.medscape.comGranulomatosis with polyangiitis - Symptoms, diagnosis and
WEBSep 18, 2024 · Granulomatosis with polyangiitis (formerly known as Wegener's granulomatosis) is a rare form of systemic vasculitis. Anti-neutrophil cytoplasmic antibody testing may help with diagnosis, but is not reliable for monitoring disease activity.
Bestpractice.bmj.com