Results 21 to 30 of about 45,538 (193)

Wegener's Granulomatosis: Strawberry Gums of the Oral Cavity

Proceedings of Singapore Healthcare, 2012
Wegener's Granulomatosis is a rare and potentially life-threatening vasculitic disease of unknown origin. The diagnosis of Wegener's Granulomatosis is made on the basis of clinical presentation, positivity for serum c-ANCA and histologic examination of ...
Hoe Kit Chee MDS (Periodontology), MRD RCSEd
doaj   +1 more source

A CLINICAL CASE OF NECROTIZING SCLERITIS ASSOCIATED WITH WEGENE R’S GRANULOMATOSIS DETECTED FOR THE FIRST TIME IN OPHTHALMOLOGICAL PRACTICE

Актуальные проблемы теоретической и клинической медицины, 2023
Granulomatosis with polyangiitis (GPA or Wegener's granulomatosis) is a rare systemic autoimmune disease of unknown etiology characterized by granulomatous inflammation, tissue necrosis, and vasculitis of small to medium-sized vessels.
A. Ulzhitaeva, M. Kusainov, G. Sagidollova, G. Karamurzaeva, A. Moldasheva, B. Allaziev   +5 more
doaj   +1 more source

Bilateral Facial Paralysis and Otitis Media as the First Presentations of Wegener’s Granulomatosis: A Case Report [PDF]

Hospital Practices and Research, 2017
Introduction: Cranial nerve palsy in Wegener’s granulomatosis is a curious incident, particularly if it occurs without kidney or lung involvement. In a review of medical articles, only 1 case of Wegener’s granulomatosis with bilateral facial nerve palsy ...
Seyed Mohammad Javad Hosseini, Jaleh Yousefi, Habib Yaribeygi, Gholam Hossein Alishiri   +3 more
doaj   +1 more source

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

Esophageal Involvement in Wegener’s Granulomatosis: A Case Report and Review of the Literature

Canadian Journal of Gastroenterology, 2000
Wegener’s granulomatosis is characterized by a granulomatous arteritis involving the upper and lower respiratory tracts, progressive glomerulonephritis and systemic symptoms attributable to small vessel vasculitis.
Glen A Fallows, Sean F Hamilton, Douglas S Taylor, S Bharati Reddy   +3 more
doaj   +1 more source

"Wegener’s granulomatosis in a patient with Rheumatoid arthritis " [PDF]

Acta Medica Iranica, 2001
Wegener’s Granulomatosis is a necrotizing granulomatous vasculitis involving small and medium sized vessels. The syndrome is classically defined as having involvement of kidney, lungs and upper respiratory tract (i.e. sinuses).
"Ahmadi Nejad Z, Gransar A, Jabbari H, Taj M "   +3 more
doaj   +1 more source

Exophthalmos as a Presenting Manifestation of Limited Wegener's Granulomatosis in a Patient with Prior Graves' Disease

Clinical Medicine Insights: Case Reports, 2009
Wegener's granulomatosis is a granulomatous necrotizing vasculitis characterized by its predilection to affect the upper and lower respiratory tracts and kidneys.
Brian Bowers, Deepak Gupta, Hirenkumar Patel, Naureen Mirza   +3 more
doaj   +1 more source

Anaesthetic Management of Subglottic Stenosis in Granulomatosis with Polyangiitis

Airway, 2021
Granulomatosis with polyangiitis, earlier known as Wegener's granulomatosis, is an autoimmune vascular disorder in which small- and medium-sized vessels are affected.
Milin Shah, Hemlata Kapoor
doaj   +1 more source

Wegener's Granulomatosis presenting with an abscess in the parotid gland: a case report

Journal of Medical Case Reports, 2009
Introduction Wegener's Granulomatosis is a vasculitis of uncertain aetiology. Affected patients usually present with disease of the respiratory and renal tracts.
Geyer Marcel, Kulamarva Gautham, Davis Anne   +2 more
doaj   +1 more source

Wegener’s granulomatosis in a middle-aged woman presenting with dyspnea, rash, hemoptysis and recurrent eye complaints: a case report

Journal of Medical Case Reports, 2012
Introduction Wegener’s granulomatosis presenting as diffuse alveolar hemorrhage is uncommon. However, the recognition of multisystem disease involving joints, kidney, eye and lung is critical for diagnosing Wegener's vasculitis.
Cardenas-Garcia Jose, Farmakiotis Dimitrios, Baldovino Berta-Paola, Kim Peter   +3 more
doaj   +1 more source