{"id":11374,"date":"2025-07-26T22:24:15","date_gmt":"2025-07-26T20:24:15","guid":{"rendered":"https:\/\/valintermed.com\/?p=11374"},"modified":"2025-07-26T22:24:15","modified_gmt":"2025-07-26T20:24:15","slug":"granulematoz-vegenera","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/vegener-s-granulomatosis\/","title":{"rendered":"Wegener's granulomatosis"},"content":{"rendered":"
<\/div>\n

Wegener's granulomatosis (WG) is a rare but serious autoimmune disease characterized by systemic inflammation, primarily affecting the respiratory tract, lungs, and kidneys. This disease belongs to the group of vasculitis, but can also affect other organs, including the skin, eyes, and nervous system. The pathogenetic basis of granulomatosis is a necrotizing granulomatous inflammatory process, which leads to tissue destruction and functional impairment. Despite its rarity, in the absence of timely diagnosis and treatment, WG can lead to significant complications and progressive loss of function of the affected organs.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n