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Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis (WG), is a systemic disorder that involves both granulomatosis and polyangiitis. What are symptoms of Wegener's granulomatosis? How is Wegener's granulomatosis diagnosed? Outline • Features of Wegener’s Granulomatosis • Patient Presentation • Imaging Findings in Our Patient – Pulmonary Involvement – Renal Involvement Read about symptoms, causes, diagnosis and treatment of granulomatosis with polyangiitis (GPA or Wegener's granulomatosis), a rare type of vasculitis. When the … Granulomatosis de Wegener 122 Gac Méd Méx Vol. 146 No. 2, 2009 infiltrado pulmonar y hemoptisis, 17 cuya frecuencia es de 5 a 45%, con mal pronóstico y … ABSTRACT. Wegener's granulomatosis is characterized by granulomatous necrotizing vasculitis that primarily affects the airways (upper and lower) and the kidneys. Five cases of pregnancy occurring in three women with previously diagnosed Wegener's granulomatosis are described. The disease was diffuse in one case and localised 7º Congreso Virtual Hispanoamericano de Anatomía Patológica http://www.conganat.org/7congreso/final/vistaImpresion.asp?id_t 1 de 14 24/09/2005 … List of URLs related to Wegener's granulomatosis and other autoimmune conditions Wegener’s granulomatosis is an antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. This rare autoimmune disease is characterized by a necrotizing