Results 31 to 40 of about 21,129 (222)

Onset of granulomatosis with polyangiitis obscured by heart disease in an elderly man

open access: yesRadiology Case Reports, 2020
We describe a case of 85-year-old man who presented to the Emergency Department with sudden dyspnea. He had a past medical history of cardiomyopathy and radiography and nonenhanced computed tomography (CT) of the chest showed pulmonary edema.
C. Pace   +4 more
doaj   +1 more source

The role of the host—Neutrophil biology

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Neutrophilic polymorphonuclear leukocytes (neutrophils) are myeloid cells packed with lysosomal granules (hence also called granulocytes) that contain a formidable antimicrobial arsenal. They are terminally differentiated cells that play a critical role in acute and chronic inflammation, as well as in the resolution of inflammation and wound ...
Iain L. C. Chapple   +4 more
wiley   +1 more source

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

open access: yes, 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   +11 more
core   +2 more sources

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

open access: yesJournal 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   +5 more
doaj   +1 more source

International guidelines for the management ofANCA-associated systemic vasculitides

open access: yesСовременная 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

open access: yesJACC: 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   +7 more
doaj   +1 more source

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

open access: yes, 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

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

open access: yes, 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   +5 more
core   +2 more sources

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

open access: yesJournal 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   +4 more
doaj   +1 more source

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

open access: yesFrontiers in Medicine, 2022
Antineutrophil cytoplasmic antibody associated vasculitis includes granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis (EGPA), and microscopic polyangiitis.
Lirong Lin   +4 more
doaj   +1 more source

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