Results 11 to 20 of about 2,274 (148)

Refractory Gingival Enlargement: A Critical Oral Clue to Early-Stage Granulomatosis With Polyangiitis-A Case Report and Literature Review. [PDF]

open access: yesCase Rep Dent
Introduction Granulomatosis with polyangiitis (GPA), formerly known as Wegener′s granulomatosis, is a rare, systemic small‐vessel vasculitis characterized by necrotizing granulomatous inflammation. It classically affects the upper airway, lungs, and kidneys.
Biplob S, Amtha R, Nadiah N, Pratama R.
europepmc   +2 more sources

The role of the host—Neutrophil biology

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Neutrophilic polymorphonuclear leukocytes (neutrophils) are myeloid cells packed with lysosomal granules (hence also called granulocytes) that contain a formidable antimicrobial arsenal. They are terminally differentiated cells that play a critical role in acute and chronic inflammation, as well as in the resolution of inflammation and wound ...
Iain L. C. Chapple   +4 more
wiley   +1 more source

Wegener Granulomatosis with Oral Involvement as Primary Manifestation: A Case Study [PDF]

open access: yesJournal of Dental Materials and Techniques, 2017
Introduction: Wegener Granulomatosis is a rare multisystemic disease with an unknown cause, characterized by necrotic granulomatous lesions in respiratory tract, systemic vasculitis in small arteries and veins and necrotizing glomerulonephritis.
Mahdokht Rashed   +5 more
doaj   +1 more source

Granulomatosis with polyangiitis: A case report and brief review of literature

open access: yesRadiology Case Reports, 2021
: Granulomatosis with polyangiitis formerly known as Wegener's granulomatosis was first described by German pathologist Friedrich Wegener in 1936. It is a multi-system necrotizing noncaseating granulomatous vasculitis which affects small to medium-sized ...
Dhairya A Lakhani, MD   +6 more
doaj   +1 more source

Wegener's Granulomatosis [PDF]

open access: yesAnnals of Internal Medicine, 1974
Abstract Wegener's granulomatosis is characterized by necrotizing granulomatous vasculitis. The localized form involves The upper or lower respiratory tracts, or both; in the commoner generalized f...
S M, Wolff   +3 more
openaire   +2 more sources

Wegener granulomatosis masquerading as pneumonia

open access: yesJournal of the Belgian Society of Radiology, 2010
We report a case of an elderly patient with a limited form of Wegener granulomatosis, which simulated the clinical and imaging features of organizing pneumonia.
D J Theodorou   +5 more
doaj   +1 more source

Strawberry Gingivitis as the Primary Sign of ANCA-Negative Granulomatosis With Polyangiitis (GPA): A Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Wegener's granulomatosis (WG) could be a lethal disease if not diagnosed and managed timely. Oral involvement is rare and often presents as gingival hyperplasia with a traditional “strawberry gingivitis” appearance. Dental practitioners may be the first ones to encounter WG and may be able to prevent disease progression like the present case ...
Salari S   +4 more
europepmc   +2 more sources

Wegener's granulomatosis

open access: yesThe American Journal of Medicine, 1970
Abstract The clinical and radiographic features of Wegener's granulomatosis are outlined. A unique case is reported where the only radiographic finding in the lungs was expansile uniform consolidation of one lobe.
R, Aach, J, Kissane
  +7 more sources

Manifestaciones periodontales de la Granulomatosis de Wegener: Reporte de un caso clínico

open access: yesInternational Journal of Interdisciplinary Dentistry, 2023
La granulomatosis de Wegener o granulomatosis con Poliangitis (GPA) es una enfermedad caracterizada por inflamación y necrosis de las paredes de los vasos sanguíneos. Es de etiología desconocida, baja prevalencia y alta agresividad. Esta enfermedad puede
Natalia Tornel   +3 more
doaj   +1 more source

Multiple Splenic Infarctions Complicating Granulomatosis with Polyangiitis

open access: yesJournal of the Belgian Society of Radiology, 2015
Background: A 57-year-old patient was admitted for high-grade fever, asthenia, sweating, dry cough and diffuse arthro-myalgias. Two years earlier, elevated titers of anticytoplasmic antibodies (ANCA) of anti-proteinase 3 specificity and renal biopsy led ...
M. Kahloune   +4 more
doaj   +1 more source

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