Results 31 to 40 of about 5,850 (214)

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

open access: yesJournal 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   +3 more
doaj  

Wegener's granulomatosis [PDF]

open access: yesBritish 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   +3 more
openaire   +2 more sources

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

open access: yesAnnals 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   +4 more
doaj   +1 more source

Subglottic stenosis as a clinical manifestation of Wegener's granulomatosis in adolescents: report of a case and review of literature [PDF]

open access: yes, 2003
Wegener's Granulomatosis is a well-characterized systemic vasculitis and necrotising granulomatous inflammation of the upper, lower respiratory tracts and the kidneys.
Brasil, Osíris de Oliveira Camponês do   +5 more
core   +5 more sources

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

open access: yesAnais 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   +5 more
doaj   +1 more source

Massive, life-threatening hemoptysis due to localized granulomatosis with polyangiitis

open access: yesJournal of Cardiothoracic Surgery, 2023
Massive hemoptysis may be related to a wide spectrum of diseases whose differential diagnosis can be challenging, also due to the medical emergency condition.
Eleonora Coviello   +4 more
doaj   +1 more source

Pathologic manifestations of levamisole-adulterated cocaine exposure. [PDF]

open access: yes, 2015
UnlabelledRheumatic manifestations of cocaine have been well described, but more recently, a dramatic increase in the levamisole-adulterated cocaine supply in the United States has disclosed unique pathologic consequences that are distinct from pure ...
Jen, Kuang-Yu, Nolan, Amber L
core   +1 more source

Granulomatose de Wegener – Envolvimento otológico, nasal, laringotraqueal e pulmonar

open access: yesRevista Portuguesa de Pneumologia, 2009
Resumo: A granulomatose de Wegener é uma vasculite sistémica rara e idiopática caracterizada pelo atingimento dos pequenos vasos. A doença atinge, preferencial-mente, as vias aérea superior e inferior e os rins, levando à formação de granulomas e
Sandra Figueiredo   +7 more
doaj   +1 more source

Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report

open access: yesJournal of Clinical Periodontology, EarlyView.
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple   +30 more
wiley   +1 more source

Granulomatosis with polyangiitis patient with retinitis as an initial manifestation

open access: yesThe Pan-American Journal of Ophthalmology, 2022
The German pathologist Friedrich Wegener described granulomatosis with polyangiitis (GPA), formerly known as Wegener's Granulomatosis, in 1936. Lesions are inflammatory, and typically include vasculitis, necrosis, and granulomatous changes.
Valdez Melo Dos Anjos Filho   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy