Results 21 to 30 of about 50,602 (199)

Current and future prospects in the management of granulomatosis with polyangiitis (Wegener's granulomatosis) [PDF]

, 2014
Ruth M Tarzi, Charles D PuseyRenal and Vascular Inflammation Section, Department of Medicine, Imperial College, London, UKAbstract: Granulomatosis with polyangiitis (GPA, formerly Wegener's granulomatosis) is a multisystem autoimmune condition ...
Pusey CD, Tarzi RM, Tarzi, Ruth M, Pusey, Charles D   +3 more
core   +1 more source

Gravidez e granulomatose de Wegener: urn caso clinic

Revista Portuguesa de Pneumologia, 1998
RESUMO: A granulomatose de Wegener (GW) é uma vasculite com manifestações multissistémicas, atingindo frequentemente o aparelho respiratório, e o rim.Descreve-se um caso clinico cuja manifestação inaugural da doença ocorreu no pulmão (hemorragia alveolar
P. Monteiro, P. Azevedo, G. Brum, A.C. Mendes, F. Monteiro, J. Monteiro, J. Valença   +6 more
doaj   +1 more source

Wegener Granulomatosis Complicated by Brain Abscess Caused by Nocardia spp. [PDF]

, 2016
Wegener granulomatosis is a multisystemic disease associated with high mortality rate and characterized by necrotizing granulomatous vasculitis predominantly in the respiratory tract and kidneys.
Aydin, Mehtap, Sahin, Sevgi, Kiziltas, Safak, Balcan, Baran   +3 more
core   +1 more source

Pioderma gangrenoso como manifestación cutánea de granulomatosis con poliangeítis. A propósito de un caso

Revistas Argentina de Medicina, 2022
La granulomatosis con poliangeítis es una vasculitis necrosante de causa desconocida que afecta a vasos de mediano y pequeño calibre. Se asocia a anticuerpos de neutrófilo (ANCA). Afecta con más frecuencia el aparato respiratorio y renal.
Carla Romina Lamolla
doaj   +2 more sources

Wegener's granulomatosis [PDF]

British Journal of Ophthalmology, 2003
Wegener's granulomatosis (WG) is a systemic granulomatous inflammatory disease of unknown origin. It occurs at any age, with the peak incidence in the third and fourth decades. The classic diagnostic triad of WG is necrotising granuloma of the upper or lower respiratory tract, vasculitis, and nephritis.
K S, Lim, G A, Lee, C E, Pavesio, L A, Ficker   +3 more
openaire   +2 more sources

Wegener granulomatosis as possible cause of vertigo: case report and review

B-ENT, 2015
Wegener granulomatosis as possible cause of vertigo: case report and review. Objective: Wegener granulomatosis (WG) or granulomatosis with polyangiitis (GPA) is a multi-system necrotizing granulomatous vasculitis that classically affects the upper ...
J. Goderis, S. De Schepper, P. Vannieuwenhuyze, B. Schmelzer   +3 more
doaj   +2 more sources

An Atypical Presentation of Wegener's Granulomatosis in a Child [PDF]

Journal of Krishna Institute of Medical Sciences University, 2016
Wegener`s granulomatosis is an autoimmune small vessel necrotising vasculitis associated with both granulomatosis and polyangiitis. While its standard form involves the upper and lower respiratory tracts and kidneys, it may essentially involve any ...
Rohit Bannerji, Avijit Mandal, Monjori Mitra , Jaydeb Ray   +3 more
doaj  

Chronic meningitis with multiple cranial neuropathies: A rare initial presentation of Wegener′s granulomatosis

Annals of Indian Academy of Neurology, 2013
Wegener′s granulomatosis (WG) is a systemic necrotizing vasculitis that affects the small blood vessels. It mainly affects the upper and lower respiratory tract and kidneys.
Vikas Gupta, Anjani Kumar Sharma, Rajendra Kumar Sureka, Sushant Kumar Bhuyan, Prashant Kumar Singh   +4 more
doaj   +1 more source

Wegener Granulomatosis: Operated Nasal Septal Perforation [PDF]

, 2018
Wegener’s granulomatosis is an idiopathic necrotizing granulatous vasculitis that can hold small and medium arteries, upper respiratory tract, lung and kidney involvement. It’s an ANCA associated vasculitis. c-ANCA positivity is considered very sensitive.
Mahi Balci, Rahmi Kilic, Şimşek, Gökce, Akay, Hatice Güzelküçük, Balcı, Mahi, Kılıç, Rahmi, Taş, Burak Mustafa, Hatice Guzelkucuk Akay, Burak Mustafa Tas, Gokce Simsek   +9 more
core   +1 more source

Multiple cavitary pulmonary nodules in association with pyoderma gangrenosum: case report Múltiplos nódulos pulmonares cavitados em associação com pioderma gangrenoso: relato de caso

Anais Brasileiros de Dermatologia, 2012
Pyoderma gangrenosum is a rare neutrophilic disease of unknown origin that is associated with systemic diseases in 50% of cases. It is characterized by erythematous-violaceous nodular lesions that quickly progress to painful ulcers, with undermined edges,
Maraya de Jesus Semblano Bittencourt, Luciana Fontenele Brito Soares, Lilia Sampaio Lobato, Alexandre Dias Mançano, Helandro Stuart Castro Leandro, Diana Mendes da Fonseca   +5 more
doaj   +1 more source