نتایج جستجو برای: anti neutrophil cytoplasmic antibody

تعداد نتایج: 585343  

2017
Alexandra C. Keefe Joseph C. Hymas Lyska L. Emerson John J. Ryan

BACKGROUND Eosinophilic granulomatosis with polyangiitis is a rare, necrotizing systemic vasculitis associated with asthma and hypereosinophilia. Its cause and pathophysiology are still being elucidated. CASE PRESENTATION We report a case of eosinophilic granulomatosis with polyangiitis in a 50-year-old Caucasian woman who presented with chest pain, dyspnea at rest, fever, and periorbital swe...

Journal: :Journal of the Royal Society of Medicine 2003

2014
Rajaie Namas Bernard Rubin Wamidh Adwar Alireza Meysami

Case. We report a rare case of hydralazine-induced anti-neutrophil cytoplasmic antibody-associated vasculitis. A 75-year-old African American woman with history of high blood pressure on hydralazine for 3 years presented with acute onset of shortness of breath and hemoptysis. Lab workup revealed a severe normocytic anemia and a serum creatinine of 5.09 mg/dL (baseline 0.9). Bronchoscopy demonst...

2006
Nursen Duzgun Mehmet Sahin Ergin Ayaslioglu

Anti neutrophil cytoplasmic antibody (ANCA) is strongly associated with some vasculitic disorders. Behçet's disease (BD) is a systemic vasculitis of unknown etiology. In this study, ANCA was found to be positive in 8 out of 66 patients (10.2%) with BD by combination testing consisting of immunofluorescence and ELISA [one patient showed an atypical pattern by indirect immunofloresence techique, ...

The granulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis, is a pauci-immune vasculitis involving small- and medium-sized blood vessels. Classically, the patients inflicted with this disease present with a triad of necrotizing granulomatous inflammation of the respiratory tract, cutaneous necrotizing vasculitis, and glomerulonephritis (GN). The antinuclear (ANA) and...

2015
Hakeem Yusuff Ignacio Malagon Kate Robson Jas Parmar Patrick Hamilton Florian Falter

INTRODUCTION Anti-neutrophil cytoplasmic antibody positive pulmonary capillaritis complicated by diffuse alveolar hemorrhage is a potentially fatal condition for which extracorporeal membrane oxygenation can facilitate improved outcomes and potential cure. Diffuse alveolar hemorrhage can be the initial presentation of an autoimmune disorder. The management is centered on the use of immunosuppre...

Journal: :Rheumatology research 2021

Granulomatosis with polyangiitis )GPA, also known as Wegener’s( is an anti-neutrophil cytoplasmic antibody-associatedmultisystem disease characterized by necrotizing small vessel vasculitis which mainly affects the upper and lower respiratorytracts well kidneys. Involvement of central nervous system uncommon in GPA might be difficult to treat.Pituitary involvement a rare presentation GPA. Prese...

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