Results 51 to 60 of about 50,602 (199)
Granulomatosis With Polyangiitis in Otolaryngologist Practice: A Review of Current Knowledge [PDF]
Clinical and Experimental Otorhinolaryngology, 2016 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
Arthritis &Rheumatology, Volume 78, Issue 5, Page 1134-1144, May 2026.Objective The objective of the study was to determine risk factors for relapse of antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) after reinduction of remission with rituximab and discontinuation of maintenance therapy. Methods This is a post hoc analysis of the RITAZAREM clinical trial.
Ellen Romich +62 more
wiley +1 more source
Wegener\u27s granulomatosis mimicking a sternal abscess.
, 1996 Bone destruction as a manifestation of Wegener\u27s granulomatosis has been reported, but these cases were limited to the head and face. We present a case in which a sternal abscess was the initial manifestation of Wegener\u27s granulomatosis. We believe
Detterbeck, F C +6 more
core +1 more source
Frozen Eye in Granulomatosis with Polyangiitis (Wegener's)
Proceedings of Singapore Healthcare, 2013 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
doaj +1 more source
Revista Colombiana de Nefrología, 2017 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
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 5, May 2026.Histopathological analysis of an infiltrative nasal lesion, diagnostic for Extranodal NK/T cell lymphoma (ENKTL), with its characteristic angiotropism, angiodestruction, and immunohistochemical staining, including positivity for EBER. ABSTRACT Extranodal NK/T‐cell lymphoma is an aggressive malignancy, rare in Western populations, that can mimic benign ...
Leonor Dias +5 more
wiley +1 more source
Turkish Journal of Nephrology, 2019 Highest prevalence of all antineutrophil cytoplasmic antibody associated systemic vasculitides is the Wegener granulomatosis, and it’s typically characterized by a necrotizing granulomatous vasculitis of the respiratory tracts, kidneys, and skin ...
Kenan TURGUTALP +9 more
doaj
Wegener´s granulomatosis in a young patient preceded by localized cutaneous manifestations
Dermatology Reports, 2011 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
doaj +1 more source
Aortic Valve Perforation in Pediatric Granulomatosis With Polyangiitis: A Case Report
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Granulomatosis with polyangiitis, formerly Wegener's granulomatosis, is a rare antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis primarily affecting the respiratory tract and kidneys. Cardiovascular involvement, particularly valvular disease, is rare, especially in pediatric patients.
Libor Svoboda +5 more
wiley +1 more source
Internal Auditory Canal Dural Enhancement in Granulomatosis with Polyangeitis Disease
Case Reports in Neurological Medicine, 2018 Diffuse dural enhancement of the internal auditory canal in T1-weighted gadolinium-enhanced magnetic resonance imaging could be a helpful and early clinical sign in a very aggressive limited granulomatosis with polyangeitis disease, called previously ...
Juan Carlos Izquierdo Velásquez +1 more
doaj +1 more source