Results 31 to 40 of about 21,257 (220)

The incidence, prevalence and mortality of granulomatosis with polyangiitis in the UK Clinical Practice Research Datalink [PDF]

, 2016
Objectives: To estimate the incidence, prevalence and mortality of Granulomatosis with polyangiitis (GPA) in the United Kingdom. Methods: We conducted a historical cohort study using data from the Clinical Practice Research Datalink and Hospital Episode
Crooks, Fiona A. Pearce, Herlyn, Knight, Lewis, Matthew J. Grainge, Ntatsaki, Peter C. Lanyon, Richard A. Watts, Richard B. Hubbard, Takala, Takala   +11 more
core   +2 more sources

Simultaneous unilateral presentation of three different ocular manifestations of granulomatosis with polyangiitis

Journal of Ophthalmic & Vision Research, 2018
Purpose: To report the simultaneous presentation of three ocular manifestations of granulomatosis with polyangiitis in one eye. Case Report: A 42-year-old man with a confirmed diagnosis of granulomatosis with polyangiitis was referred to the emergency ...
Ali Salehi, Farzan Kianersi, Heshmatollah Ghanbari, Zahra Dastborhan, Ebrahim Gerami, Elnaz Pirmoazzen   +5 more
doaj   +1 more source

International guidelines for the management ofANCA-associated systemic vasculitides

Современная ревматология, 2019
The paper deals with international guidelines for the management of antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitides (SVs) that are a group of severe life-threatening immune-mediated diseases. This group includes granulomatosis
T. V. Beketova
doaj   +1 more source

GPA-Induced Granulomatous Endocarditis Mimicking a Thrombotic Mitral Valve Stenosis

JACC: Case Reports, 2020
We present the case of a patient with granulomatous endocarditis of the mitral valve leading to severe valve stenosis caused by granulomatosis with polyangiitis.
Christoph Marquetand, MD, Peter Lamprecht, MD, Franz F. Dressler, MD, Sven Perner, MD, PhD, Konstanze Holl-Ulrich, MD, Ulrich Stierle, MD, Anas Aboud, MD, Jan-Christian Reil, MD   +7 more
doaj   +1 more source

Association of ANCA associated vasculitis and rheumatoid arthritis: a lesser recognized overlap syndrome [PDF]

, 2015
Background ANCA associated vasculitis (AAV) is an autoimmune disease with significant morbidity and mortality, in which diagnostic delay is associated with worse outcomes. AAV is rarely found in association with other immune mediated diseases.
Draibe, J, Salama, AD
core   +2 more sources

ANCA-associated vasculitis – Should we change the standard of care? [PDF]

, 2015
Collaborative clinical trials over the last 25 years have revolutionised the care of patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. This has led to production of management recommendations and standards of care.
Bligny, Bourgarit, Choi, de Groot, De Groot, Fauci, Faurschou, Finkielman, Flossmann, Ghosh, Guillevin, Han, Harper, Hauer, Hoffman, Jayne, Jennette, Jennette, Koldingsnes, Leavitt, Luqmani, Mahr, Masi, Mooney, Mooney, Mukhtyar, Mukhtyar, Mukhtyar, Mukhtyar, Nataraja, Ntatsaki, Pagnoux, Pradhan, Rahmattulla, Rao, Reinhold-Keller, Sharma, Sorensen, Stone, Stone, Suppiah, Talar-Williams, Walsh, Watts, Watts, Watts   +45 more
core   +1 more source

Granulomatosis with polyangiitis in a patient with polydipsia, facial nerve paralysis, and severe otologic complaints: a case report and review of the literature

Journal of Medical Case Reports, 2022
Background Granulomatosis with polyangiitis, formerly known as Wegener granulomatosis, is a necrotizing vasculitis with granulomatous inflammation that belongs to the class of antineutrophil cytoplasmic antibodies-positive diseases.
Lukas Koenen, Ulf Elbelt, Heidi Olze, Sören Zappe, Steffen Dommerich   +4 more
doaj   +1 more source

Eosinophilic Granulomatosis With Polyangiitis Presenting With Oral Granuloma as the Initial Symptom: A Case Report

Frontiers in Medicine, 2022
Antineutrophil cytoplasmic antibody associated vasculitis includes granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis (EGPA), and microscopic polyangiitis.
Lirong Lin, Rongjie Yu, Luquan Zheng, Shuyu Gong, Jurong Yang   +4 more
doaj   +1 more source

An uncommon presentation of eosinophilic granulomatosis with polyangiitis: a case report [PDF]

, 2014
INTRODUCTION: Eosinophilic granulomatosis with polyangiitis is a rare and potentially fatal disease if not readily diagnosed. Cerebral involvement is extremely rare and clinical presentation as hemorrhagic stroke is even rarer.
Andolina, G, Banco, MA, Bonura, A, BUSCEMI, Silvio, COSTANZA GAGLIO, Edy, TAORMINA, Giuseppe   +5 more
core   +2 more sources

Childhood-onset granulomatosis with polyangiitis and microscopic polyangiitis: systematic review and meta-analysis

Orphanet Journal of Rare Diseases, 2016
Background The data from cohorts of childhood-onset granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) remain scarce and heterogeneous. We aimed to analyse the features at presentation, therapeutic approaches and the disease course
Michele Iudici, Pierre Quartier, Benjamin Terrier, Luc Mouthon, Loïc Guillevin, Xavier Puéchal   +5 more
doaj   +1 more source