Results 41 to 50 of about 2,274 (148)
Cytomegalovirus retinitis presenting as vasculitis in a patient with Wegener’s granulomatosis
Paris G Tranos1, Ilias Georgalas2, Panagiota Founti1, Ioannis Ladas21Papageorgiou University Hospital, Thessaloniki, Greece; 2Department of Ophthalmology, “G.Genimatas” Hospital, Athens, GreecePurpose: To present an unusual case of ...
Paris G Tranos +3 more
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Granulomatosis with Polyangiitis (Wegener Granulomatosis) Mimicking Infective Endocarditis
Introduction Infective endocarditis (IE) has been reported to mimic granulomatosis with polyangiitis (GPA) and to test positive to antineutrophil cytoplasmic antibodies (ANCA), which may lead to a misdiagnosis and inappropriate treatment.
Imène Rachdi +6 more
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ABSTRACT A 65‐year‐old woman presented to a tertiary care center with a classical clinical scenario—3 months of persistent, right‐sided frontal headache. Over the course of 20 days, a right‐sided frontal headache developed into ptosis of the right upper eyelid.
Saiful Islam Chowdhury +6 more
wiley +1 more source
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
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ABSTRACT Timely diagnosis of type 1 diabetes (T1D), especially in high‐risk populations, is crucial for preventing serious health complications. T1D is a chronic progressive autoimmune disease that has presymptomatic stages that can be identified through the detection of islet autoantibodies. Given that T1D is associated with other autoimmune diseases,
Nick Thomas +8 more
wiley +1 more source
Frozen Eye in Granulomatosis with Polyangiitis (Wegener's)
Ocular involvement in Granulomatosis with Polyangiitis (GP or Wegener Granulomatosis) is a potentially serious disease manifestation which needs prompt diagnosis and treatment.
Qin Yan MRCP +2 more
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El presente manuscrito se hace con el fin de reportar un caso del tema en mención y realizar una revisión de la literatura disponible más reciente con respecto al diagnóstico y tratamiento. Antecedentes La granulomatosis de Wegener (GW) se caracteriza
José Luis Fabris Vargas +4 more
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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
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ANCA‐Negative Granulomatosis With Polyangiitis Mimicking Sinusitis and Rhinoscleroma: A Case Report
Introduction This case details the diagnostic challenge of ANCA‐negative granulomatosis with polyangiitis (GPA) initially presenting as refractory chronic rhinosinusitis, mimicking recurrent infections, and other granulomatous conditions. It highlights the potential for significant diagnostic delay when serological markers are absent.
Sergey Gorbunov +2 more
wiley +1 more source
Wegener´s granulomatosis in a young patient preceded by localized cutaneous manifestations
Wegener´s granulomatosis (WG) is a rare, systemic vasculitis involving multiple organs. The clinical presentation is highly diverse, and there is considerable risk of mortality if diagnosis and treatment are delayed.
Jesper Smit +3 more
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