Results 11 to 20 of about 64,510,463 (206)

Tension Pneumothorax as Initial Manifestation of Granulomatosis with Polyangiitis (GPA) [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2021
Granulomatosis with polyangiitis (Wegener’s granulomatosis) is a systemic vasculitis that primarily affects small and medium vessels. Its manifestations are usually confined to the upper airway, lower airway and kidney.
Rúben Reis   +5 more
doaj   +2 more sources

Pyoderma Gangrenosum-like Ulcers Associated Granulomatosis with Polyangiitis [PDF]

open access: yesCase Reports in Clinical Practice
Granulomatosis with polyangiitis is an ANCA-positive vasculitis primarily affecting small to medium-sized vessels, typically involving the lungs and kidneys.
Katia Fabiola Avila   +3 more
doaj   +2 more sources

Granulomatosis with Polyangiitis Presenting with Coronary Artery and Pericardial Involvement [PDF]

open access: yesCase Reports in Radiology, 2015
Granulomatosis with polyangiitis is a systemic disease resulting in necrotizing vasculitis of small- and medium-sized vessels. Cardiac involvement is rare and when present usually manifests with pericarditis and coronary artery vasculitis. We report here
Rohit Dewan   +3 more
doaj   +2 more sources

Pituitary granulomatosis with polyangiitis [PDF]

open access: yesBMJ Case Reports, 2013
Granulomatosis with polyangiitis (GPA) is a small vessel vasculitis that can affect several organs, most commonly the respiratory tract and kidneys. Pituitary involvement is exceptionally rare. Most case reports of GPA of the pituitary gland have been described in middle-aged women who have concomitant ears, nose and throat involvement.
Hannah, Slabu, Terra, Arnason
openaire   +2 more sources

Chronic Rhinosinusitis and Nasal Polyps in Eosinophilic Granulomatosis With Polyangiitis: A Scoping Review. [PDF]

open access: yesInt Forum Allergy Rhinol
ABSTRACT Background Chronic rhinosinusitis (CRS) is one of the most common manifestations of eosinophilic granulomatosis with polyangiitis (EGPA), often preceding the diagnosis of systemic vasculitis by several years. The sinonasal presentation of EGPA typically resembles CRS with nasal polyps (CRSwNP), making it clinically indistinguishable from those
Sharma A   +12 more
europepmc   +2 more sources

Penile granulomatosis with polyangiitis [PDF]

open access: yesJAAD Case Reports, 2019
Granulomatosis with polyangiitis (GPA) is a systemic form of vasculitis that predominantly affects small and medium-sized vessels. The organs often involved are the kidneys and respiratory tract. Diagnosis can be established based on the histologic findings of necrotizing granulomatous inflammation and vasculitis and positive test results for anti ...
Amico, Séverine   +4 more
openaire   +2 more sources

Limited granulomatosis with polyangiitis presenting as an isolated lung lesion

open access: yesIndian Journal of Pathology and Microbiology, 2020
Granulomatosis with polyangiitis (GPA) is a systemic necrotizing vasculitis involving small and medium-sized blood vessels and granulomatous inflammation of upper and lower respiratory systems and/or renal system.
Shameera Begum   +3 more
doaj   +1 more source

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

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

A rare geriatric diagnosis of Eosinophilic Granulomatosis with Polyangiitis: a case report

open access: yes, 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of systemic disease characterized by inflammation and necrotizing effects of the small and medium blood vessels. It is a vasculitis found in all age groups and both genders, although its
Emidio, Fábio C.   +4 more
core   +1 more source

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