Results 31 to 40 of about 64,510,463 (206)
Background Although gastrointestinal involvement in patients with granulomatosis with polyangiitis is uncommon, it is associated with mild to severe life-threatening complications. We present a case of pneumatosis cystoides intestinalis in a patient with
Kensuke Nakatani +6 more
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Granulomatosis With Polyangiitis in Otolaryngologist Practice: A Review of Current Knowledge [PDF]
Granulomatosis with polyangiitis (GPA) is an idiopathic vasculitis of medium and small arteries, characterized by necrotizing granulomatous inflammation. GPA typically affects upper and lower respiratory tract with coexisting glomerulonephritis.
Joanna Wojciechowska +3 more
doaj +1 more source
Relapsing granulomatosis with polyangiitis with severe lung and upper respiratory tract involvement successfully treated with rituximab [PDF]
Granulomatosis with polyangiitis (GPA) is a chronic, relapsing, primary systemic small vessel vasculitis associated with anti-neutrophil cytoplasmic antibodies. The disease is characterised by the involvement of various organs.
Anna Masiak, Zbigniew Zdrojewski
core +1 more source
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
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
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Onset of granulomatosis with polyangiitis obscured by heart disease in an elderly man
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
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
A 22-year-old female patient was admitted to hospital after being referred from the oral medicine clinic where she had been seen for persistent gingivitis and mouth ulcers. She described an insidious history of persistent fevers, dry cough and unexplained weight loss over 4–6 weeks.
openaire +3 more sources
Granulomatosis with polyangiitis – diagnostic difficulties?
Granulomatosis with polyangiitis (GPA) is characterized by necrotic vasculitis of the medium and small vessels, granuloma formation and presence of antineutrophil cytoplasmic antibodies against proteinase-3 in serum.
Marta Madej +3 more
core +1 more source
Granulomatosis with polyangiitis, formerly known as Wegener's granulomatosis, is an autoimmune antineutrophil cytoplasmic antibodies – associated systemic vasculitis with a progressive course.Granulomatosis with polyangiitis remains one of the most ...
M. A. Borodin +2 more
doaj +1 more source

