• Granulomatosis with polyangiitis (Wegener's granulomatosis) is a type of vasculitis which can be categorized as a sub-branch of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides. (rheumres.org)
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a type of vasculitis which can be categorized as a sub-branch of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides [1]. (rheumres.org)
  • Granulomatosis with polyangiitis is the third most common type of vasculitis in Iran after Behcet's disease and cutaneous leukocytoclastic angiitis [6]. (rheumres.org)
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis (WG), after the Nazi German physician Friedrich Wegener, is a rare long-term systemic disorder that involves the formation of granulomas and inflammation of blood vessels (vasculitis). (wikipedia.org)
  • Granulomatosis with polyangiitis is characterized by necrotizing granulomatous inflammation, small- and medium-sized vessel vasculitis, and focal necrotizing glomerulonephritis, often with crescent formation. (merckmanuals.com)
  • To assess the Birmingham Vasculitis Activity Score for Wegener's Granulomatosis (BVAS/WG) with respect to its selection and weighting of items. (nih.gov)
  • Wegener's granulomatosis is a form of vasculitis that affects the lungs, kidneys and other organs. (checkorphan.org)
  • Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): evolutions in classification, etiopathogenesis, assessment and management. (medscape.com)
  • Originally, the disease was named for Friedrich Wegener who discussed the disorder in 1936 [2]. (rheumres.org)
  • It is named after Dr. Friedrich Wegener, who described the disease in 1936. (checkorphan.org)
  • The model was tested using the Wegener's Granulomatosis Etanercept Trial (WGET) cohort. (ox.ac.uk)
  • This study used the BVAS/WG data from the Wegener's Granulomatosis Etanercept Trial. (nih.gov)
  • If you or a loved one has been diagnosed with Wegener's Granulomatosis or Granulomatosis with Polyangiitis (GPA), it's important to learn as much as possible about this chronic autoimmune disease in order to better manage your symptoms and treatment plan. (articleinsider.com)
  • Wegener's Granulomatosis and Granulomatosis with Polyangiitis are two different names for the same disease, which is an autoimmune disorder that primarily affects the blood vessels in the lungs, kidneys, and upper respiratory tract. (articleinsider.com)
  • The medical records of patients admitted to the Department and Clinic of Rheumatology who were diagnosed with granulomatosis with polyangiitis between January 1, 2006 and December 31, 2016 were retrospectively studied. (rheumres.org)
  • Patients were classified according to the American College of Rheumatology (ACR) 1990 classification criteria for Wegener's granulomatosis. (rheumres.org)
  • Patients were classified according to the American College of Rheumatology (ACR) 1990 classification criteria for Wegener's granulomatosis [8] and 2012 Revised International Chapel Hill Consensus Conference Nomenclature [1]. (rheumres.org)
  • Efficacy of Rituximab for Otolaryngologic (ENT) Manifestations of Granulomatosis with Polyangiitis (GPA, Wegener's granulomatosis), American College of Rheumatology Annual Scientific Meeting, San Diego, CA, Oct 25-30, 2013. (hss.edu)
  • This study examined the demographic, clinical, radiographic and laboratory characteristics of patients with granulomatosis with polyangiitis (GPA) in Imam Reza Hospital, Mahshad, Iran. (rheumres.org)
  • Granulomatosis with polyangiitis (Wegener): clinical aspects and treatment. (medscape.com)
  • Clinical features of childhood granulomatosis with polyangiitis (Wegener's granulomatosis). (printo.it)
  • Szpirt WM, Heaf JG, Petersen J. Plasma exchange for induction and cyclosporine A for maintenance of remission in Wegener's granulomatosis - a clinical randomized controlled trial. (smw.ch)
  • Granulomatosis with polyangiitis is usually suspected only when a person has had unexplained symptoms for a long period of time. (wikipedia.org)
  • Wegener's granulomatosis is usually only suspected when a patient has had unexplained symptoms for a long period of time. (checkorphan.org)
  • Wegener's Granulomatosis and Granulomatosis with Polyangiitis are essentially the same disease, with the latter being the more modern name for the condition. (articleinsider.com)
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a rare disease. (medlineplus.gov)
  • To assess the correlation and prognostic value of antineutrophil cytoplasmic antibody (cANCA) titers with disease activity in patients with Wegener's granulomatosis (WG). (nih.gov)
  • Introduction Granulomatosis is a medical term for a disease where granulomas - or clusters of certain cell types - are formed. (bmj.com)
  • OBJECTIVE: To identify serum ion patterns that distinguish remission from active disease in patients with Wegener's granulomatosis (WG). (duke.edu)
  • Walker s health odyssey began in 1995, when he was diagnosed with Wegener s Granulomatosis, an uncommon disease that is even more rare among African Americans. (handsonhealth-sc.org)
  • Objective This study was conducted to evaluate the efficacy and safety of repeated and prolonged B cell depletion with rituximab (RTX) for the maintenance of long-term remission in patients with chronic relapsing granulomatosis with polyangiitis (Wegener's) (GPA). (elsevierpure.com)
  • Although the structure of the granulomas and multinucleated giant cells in granulomatosis with polyangiitis (GPA) is known, little is established about what drove granuloma formation and why it is infrequently found in patients with myeloperoxidase-antineutrophil cytoplasm antibodies. (bmj.com)
  • Wegener's granulomatosis: studies in eighteen patients and a review of the literature. (smw.ch)
  • Wegener granulomatosis: an analysis of 158 patients. (smw.ch)
  • Anticytoplasmic antibodies (ACPA) against myelomonocytic cells were demonstrable in 54 of 72 patients with Wegener's granulomatosis (WG). (uni-luebeck.de)
  • The standard treatment for Wegener's granulomatosis is cyclophosphamide and high dose corticosteroids for remission induction and less toxic immunosuppressants like azathioprine, leflunomide, methotrexate or mycophenolate mofetil. (checkorphan.org)
  • Wegener's granulomatosis is part of a larger group of vasculitic syndromes, all of which feature the presence of an abnormal type of circulating antibody termed ANCAs (antineutrophil cytoplasmic antibodies) and affect small and medium-size blood vessels. (checkorphan.org)
  • Although Wegener's granulomatosis affects small and medium-sized vessels, it is formally classified as one of the small vessel vasculitides in the Chapel Hill system. (checkorphan.org)
  • These granulomas are the main reason for the appellation of "Wegener's granulomatosis," although it is not an essential feature. (checkorphan.org)
  • A systematic review of 84 trials examined the evidence for various treatments in Wegener's granulomatosis. (checkorphan.org)
  • Sinonasal Wegener granulomatosis: a single-institution experience with 120 cases. (medscape.com)
  • [ 1 ] A retrospective review of 34 cases of DAH revealed nearly one-third of the cases were caused by Wegener granulomatosis. (medscape.com)
  • Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome). (upmc.com)
  • The differential diagnosis also includes rare vascular etiologies such as lupus pneumonitis, eosinophilic granulomatosis with polyangiitis, idiopathic pulmonary hemosiderosis, IgA nephropathy, hypersensitivity pneumonitis, pulmonary artery rupture, and diffuse alveolar hemorrhage. (appliedradiology.com)
  • Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): evolutions in classification, etiopathogenesis, assessment and management. (medscape.com)
  • Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis ) (single case reports). (altmeyers.org)
  • Wegener's granulomatosis: prospective clinical and therapeutic experience with 85 patients for 21 years. (medscape.com)
  • Elevated relapse rate under oral methotrexate versus leflunomide for maintenance of remission in Wegener's granulomatosis. (medscape.com)
  • Granulomatosis with polyangiitis (Wegener's): an alternative name for Wegener's granulomatosis. (medscape.com)
  • The American College of Rheumatology 1990 criteria for the classification of Wegener's granulomatosis. (medscape.com)
  • Granulomatosis with polyangiitis (GPA) - formerly known as Wegener's granulomatosis - is a rare form of vasculitis. (patient.info)
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a rare disease. (medlineplus.gov)
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis (WG), after the Nazi German physician Friedrich Wegener, is a rare long-term systemic disorder that involves the formation of granulomas and inflammation of blood vessels (vasculitis). (wikipedia.org)
  • Background Granulomatosis with polyangiitis (GPA) formerly known as Wegener's granulomatosis (WG) belongs to the group of ANCA-associated necrotizing vasculitides. (researchensemble.com)
  • Keywords: Wegener's granulomatosis Granulomatosis with polyangiitis Clinical research Clinical picture of disease Evaluation with books Background Granulomatosis with polyangiitis (GPA) previously referred to as Wegener's granulomatosis (WG) [1] is normally a necrotizing vasculitis impacting predominantly little vessels. (researchensemble.com)
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a rare and life-threatening disorder that restricts the blood flow to several organs, including the lungs, kidneys, and upper respiratory tract. (medicalnewstoday.com)
  • CHCC2012 also agreed to rename Wegener's granulomatosis as granulomatosis with polyangiitis (GPA). (medicalnewstoday.com)
  • 10. Cutaneous manifestations of Wegener's granulomatosis: a clinicopathologic study of 17 patients and correlation to antineutrophil cytoplasmic antibody status. (nih.gov)
  • 19. Wegener's granulomatosis associated with renal cell carcinoma. (nih.gov)
  • 20. Renal histology in Chinese patients with anti-myeloperoxidase autoantibody-positive Wegener's granulomatosis. (nih.gov)
  • Herein we describe a well-substantiated case of cyclophosphamide-induced hepatotoxicity in a patient with Wegener's granulomatosis. (nih.gov)
  • Cyclophosphamide-induced hepatitis in Wegener's granulomatosis. (nih.gov)
  • Diffuse histiocytic lymphoma in a patient treated with cyclophosphamide for Wegener's granulomatosis. (nih.gov)
  • For example, Wegener's granulomatosis is now more commonly termed, granulomatosis with polyangiitis, which is more pathophysiologically relevant [1]. (medscimonit.com)
  • He developed effective therapies for formerly fatal inflammatory and immune-mediated diseases such as polyarteritis nodosa, granulomatosis with polyangiitis (formerly Wegener's granulomatosis), and lymphomatoid granulomatosis. (nih.gov)
  • Wegener's granulomatosis may be fatal without prompt medical treatment. (bookriff.com)
  • Effect of cyclophosphamide upon the immune response in Wegener's granulomatosis. (ama-assn.org)
  • Wegener's Granulomatosis A rare, autoimmune, systemic medium and small size vasculitis. (nih.gov)
  • Can you still be diagnosed with Granulomatosis with polyangiitis (GPA, formerly Wegener's) if the ANCA is negative? (vasculitisfoundation.org)
  • Although ANCA is elevated in a majority of patients with granulomatosis with polyangiitis (GPA, formerly called Wegener's), it is not detectable in all patients and is not necessary to make the diagnosis. (vasculitisfoundation.org)
  • Your ticket for the: Can you still be diagnosed with Granulomatosis with polyangiitis (GPA, formerly Wegener's) if the ANCA is negative? (vasculitisfoundation.org)
  • The subtype c-ANCA, shows cytoplasm staining by IFA and is diagnostic for Wegener granulomatosis. (rapidtest.com)
  • PR3 is the most common antigen target of ANCA in patients with granulomatosis with polyangiitis where c-ANCA is found over 90% of the time. (rapidtest.com)
  • Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis. (cdc.gov)
  • Granulomatosis with polyangiitis is characterized by necrotizing granulomatous inflammation, small- and medium-sized vessel vasculitis, and focal necrotizing glomerulonephritis, often with crescent formation. (msdmanuals.com)
  • Granulomatosis with polyangiitis (Wegener's) (GPA) is a systemic inflammatory disease that is characterized by necrotizing, granulomatous inflammation and vasculitis of the small to medium-sized vessels. (nih.gov)
  • When patients present with a limited form of granulomatosis with polyangiitis (GPA) that includes upper airway disease, orbital disease, or pulmonary disease, the differential diagnosis may include infectious and neoplastic diseases and other forms of vasculitis. (medscape.com)
  • It significantly impacts my condition, vasculitis (granulomatosis with polyangiitis/Wegener's and chronic periaortitis). (themighty.com)
  • Granulomatosis with polyangiitis, while more commonly identified in adults, should be suspected in children presenting with hemoptysis, hematuria, and chest imaging showing cavitary pulmonary nodules, ground-glass opacity, and consolidation. (appliedradiology.com)
  • Granulomatosis with polyangiitis (GPA, formerly called Wegener's) is a rare disease of uncertain cause. (bookriff.com)
  • The signs found in granulomatosis with polyangiitis occur as a result of the inflammation of the small vessels and may affect any part of the body. (patient.info)