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Wegener's granulomatosis - PubMed
Wegener's granulomatosis is an organ- and/or life-threatening autoimmune disease of as yet unknown etiology. The classic clinical triad consists of necrotizing granulomatous inflammation of the upper and/or lower respiratory tract, necrotizing glomerulonephritis, and an autoimmune necrotizing systemic vasculitis affecting predominantly small vessels.
Pubmed.ncbi.nlm.nih.govDA: 23 PA: 10 MOZ Rank: 33
Granulomatosis with Polyangiitis (GPA, formerly called Wegener’s)
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. Appointments & Access.
My.clevelandclinic.orgDA: 22 PA: 50 MOZ Rank: 49
Wegener’s Granulomatosis - Laryngopedia | Dr. Robert Bastian
Wegener’s granulomatosis is a rare autoimmune disorder in which blood vessels become inflamed. The inflammation causes swelling and scarring. Three typical organs attacked are sinus/nasal cavities, lungs, and kidneys. In the forme fruste variant, it is mostly an inflammatory stenosis (narrowing) of the area below the vocal folds, and also the trachea. A person …
Laryngopedia.comDA: 16 PA: 25 MOZ Rank: 43
Granulomatosis with Polyangiitis (Wegener's) Symptoms, …
Granulomatosis with polyangiitis is a rare disease in which blood vessels become inflamed (a condition called vasculitis) and localized, nodular collections of abnormal inflammatory cells, known as granulomas, are found in affected tissues.; Granulomatosis is the term that refers to the presence of granulomas, which are small areas of inflammation filled with immune …
Emedicinehealth.comDA: 23 PA: 38 MOZ Rank: 64
Granulomatosis with polyangiitis - Wikipedia
Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis (WG), is a rare long-term systemic disorder that involves the formation of granulomas and inflammation of blood vessels (vasculitis). It is a form of vasculitis that affects small- and medium-size vessels in many organs but most commonly affects the upper respiratory tract, lungs and kidneys.
En.wikipedia.orgDA: 16 PA: 38 MOZ Rank: 58
Granulomatosis with Polyangiitis (GPA) - Arthritis Society
Granulomatosis with polyangiitis (GPA, formerly called Wegener’s granulomatosis). Although the disease can involve any organ system, it most commonly affects the upper respiratory tract (sinuses, nose, ears), lungs, kidneys, skin and nerves.
Arthritis.caDA: 12 PA: 50 MOZ Rank: 100
Wegener granulomatosis - PMC
Wegener granulomatosis, or granulomatous vasculitis, is a disease that produces inflammation of the medium and small arteries and venules ( 2 – 4 ). Necrotizing and crescentic changes are found in the glomeruli ( 1 ). The process typically affects the upper and lower airways and kidneys.
Ncbi.nlm.nih.govDA: 20 PA: 25 MOZ Rank: 51
Wegener’s granulomatosis - Health Jade
Wegener’s granulomatosis is a rare condition in which your blood vessels become inflamed. Wegener’s granulomatosis is a type of vasculitis, or inflammation of the blood vessels. Wegener’s granulomatosis involves the small and medium-sized blood vessels throughout your body. The inflammation in the blood vessel does not allow blood to flow ...
Healthjade.comDA: 14 PA: 25 MOZ Rank: 46
Wegener's Granulomatosis: Diagnosis & Treatment - Steady. Health
Granulomatosis with polyangiitis (GPA) — formerly Wegener’s granulomatosis — is a very rare disease, affecting only one in every 30,000-50,000 people.. Reviewed by Medical Team. Reviewed by Medical Team.
Steadyhealth.comDA: 20 PA: 50 MOZ Rank: 81
Granulomatosis with Polyangiitis - Merck Manuals Consumer Version
Granulomatosis with polyangiitis is most common among whites but can occur in all ethnic groups and at any age. Most people are affected at about age 40. Its cause is unknown. It resembles an infection, but no infecting organism has been identified. Collections of immune cells that cause inflammation (called granulomas) form nodules and ...
Merckmanuals.comDA: 20 PA: 50 MOZ Rank: 41
Wegener's Granulomatosis Treatment Today - The Rheumatologist
Wegener’s granulomatosis (WG) is a complex multisystem vasculitic disease of unknown cause. Although once rapidly progressive and often fatal, WG is now a manageable condition in which remission can be achieved by conventional immunosuppressive therapy. With the introduction of effective therapy by Fauci and Wolff in the 1970s and 1980s, the ...
The-rheumatologist.orgDA: 26 PA: 49 MOZ Rank: 85
Granulomatosis with Polyangiitis - Johns Hopkins Vasculitis Center
Granulomatosis with Polyangiitis is a disease involving granulomatous inflammation, necrosis and vasculitis that most frequently targets the upper respiratory tract, lower respiratory tract, and kidneys. Although Granulomatosis with Polyangiitis can begin at any age, the average age of onset is about 40 years.
Hopkinsvasculitis.orgDA: 25 PA: 50 MOZ Rank: 87
Granulomatosis with polyangiitis | Radiology Reference Article ...
Granulomatosis with polyangiitis (GPA), previously known as Wegener granulomatosis, is a multisystem necrotizing non-caseating granulomatous c-ANCA positive vasculitis affecting small to medium-sized arteries, capillaries, and veins, with a predilection for the respiratory system and kidneys. This article discusses GPA in general. For organ-specific …
Radiopaedia.orgDA: 15 PA: 42 MOZ Rank: 69
Wegener's granulomatosis - TheFreeDictionary.com
Wegener's granulomatosis: Definition Wegener's granulomatosis is a very rare disease that affects many different organs and systems of the body. It mainly attacks the respiratory system (sinuses, nose, windpipe, and the lungs) and the kidneys. One of the main features of the disease is an inflammation of the blood vessels ( vasculitis ). The ...
Medical-dictionary.thefreedictionary.comDA: 40 PA: 16 MOZ Rank: 69
Granulomatosis with Polyangiitis - NORD (National Organization …
For many years, granulomatosis with polyangiitis was known as Wegener’s granulomatosis or Wegener granulomatosis. Wegener is the surname of a physician who was one of the first to describe the disorder in detail in the medical literature back in the 1930s. Other doctors before Wegener also described the disease. Surnames don’t characterize ...
Rarediseases.orgDA: 16 PA: 48 MOZ Rank: 78
Granulomatosis with Polyangiitis (GPA, formerly Wegener …
Granulomatosis with polyangiitis (GPA), formerly known as Wegener granulomatosis, is a rare multisystem autoimmune disease of unknown etiology. Its hallmark features include necrotizing granulomatous inflammation and pauci-immune vasculitis in small- and medium-sized blood vessels (see the images below).
Emedicine.medscape.comDA: 22 PA: 24 MOZ Rank: 61
Wegener's Granulomatosis : Causes, Symptoms, Treatment and Faq's
Wegener’s granulomatosis causes systemic inflammation of blood vessels. It is an extremely rare medical condition that leads to quick inflammation of blood vessels across your body. However, the most commonly inflamed parts include the …
Healthlibrary.askapollo.comDA: 27 PA: 50 MOZ Rank: 94
Granulomatosis with polyangiitis - Symptoms, diagnosis and …
Granulomatosis with polyangiitis (formerly known as Wegener's granulomatosis) is a systemic vasculitis that typically involves small and medium vessels. Although any organ may be targeted, the classic triad consists of upper and lower respiratory tract involvement and pauci-immune glomerulonephritis. Involvement of cutaneous, ocular ...
Bestpractice.bmj.comDA: 20 PA: 17 MOZ Rank: 54
Mucocutaneous leishmaniasis masquerading as Wegener …
A biopsy was consistent with limited Wegener's granulomatosis although antineutrophil cytoplasmic antibodies were negative. Her nasal inflammation progressed despite trials of prednisone, methotrexate, and azathiop … A 43-year-old Brazilian female presented in 2001 with nasal stuffiness and sinusitis. A biopsy was consistent with limited Wegener's …
Pubmed.ncbi.nlm.nih.govDA: 23 PA: 10 MOZ Rank: 51
Wegener's Granulomatosis | BW Arthritis & Rheumatology, PA
Wegener's granulomatosis, also known as granulomatosis with polyangiitis (GPA), is a rare disease characterized by the inflammation of blood vessels. In addition to blocking blood flow to vital organs, this condition causes the formation of granulomas (inflamed masses) to form around the blood vessels, destroying normal tissue. Although this disease can be fatal if left untreated, …
Bwarthritis.comDA: 19 PA: 28 MOZ Rank: 66
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