Results 71 to 80 of about 5,939 (161)

Vasculitis of the upper airways1

Swiss Medical Weekly, 2012
Systemic vasculitides are rare and potentially life-threatening diseases. Granulomatosis with polyangiitis (GPA; formerly Wegener’s granulomatosis) and Churg Strauss syndrome (possibly to be renamed eosinophilic granulomatosis with polyangiitis ...
Christian Pagnoux, Nikolaus E Wolter
doaj   +1 more source

Eosinophilic Granulomatosis With Polyangiitis Presenting With Visual Problems and Subendocardial Fibrosis, A Case Report

Clinical Case Reports
This case highlights the atypical presentation of eosinophilic granulomatosis with polyangiitis (EGPA) with neurological and cardiac complications, emphasizing the necessity of early recognition and aggressive treatment to prevent morbidity and mortality.
Mahshid Talebi‐Taher, Sobhan Mehdipourrabori, Soroush Mostafavi, Mahboubeh Pazoki   +3 more
doaj   +1 more source

Eosinophilic granulomatosis with polyangiitis across the eosinophilic spectrum: from molecular mechanisms to practical differential diagnosis and targeted therapy

Rheumatology
Introduction Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis defined by asthma, hypereosinophilia, and multiorgan involvement.
Aleksandra Hus, Małgorzata Wisłowska
doaj   +1 more source

ANCA-associated vasculitis in the United Arab Emirates: a 17-year case series with review from Gulf literature

Annals of Saudi Medicine
BACKGROUND: Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a rare and severe autoimmune disease characterized by pauci-immune necrotizing vasculitis.
Hala Shahrour, Neama Luqman, Fatima AlKindi, Mumtaz Khan, Shamma Ahmad Al Nokhatha   +4 more
doaj   +1 more source

P-ANCA negative eosinophilic granulomatosis with polyangiitis

Respiratory Medicine Case Reports, 2019
Vasculitis refers to inflammation of the systemic vessels. Eosinophilic granulomatosis with polyangiitis (EGPA) is a medium and small vessel vasculitis characterized by hypereosinophilia, pulmonary infiltrates, difficult to treat asthma and ...
Saad Ullah, Mirza Ali, Phyo Kyaw, Faraaz Nayeemuddin, Rajagopal Sreedhar, John Gao   +5 more
doaj   +1 more source

Pediatric antineutrophil cytoplasmic antibody-associated vasculitis: A review on pulmonary manifestations, management, and outcomes

Tungs’ Medical Journal
Antineutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) is a rare systemic autoimmune disorder characterized by necrotizing inflammation of blood vessels infiltrated by neutrophils.
Chien-Heng Lin, Chieh-Ho Chen, Wei-Ching Lin, Wen-Jue Soong, Syuan-Yu Hong   +4 more
doaj   +1 more source

Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status

Nature Communications, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare inflammatory disorder characterised by asthma, eosinophilia and vasculitis. Here, the authors describe a genome-wide association study of EGPA that reveals clinical and genetic differences ...
Paul A Lyons, James E Peters, Federico Alberici, James Liley, Richard M. R. Coulson, William Astle, Chiara Baldini, Francesco Bonatti, Maria C Cid, Heather Elding, Giacomo Emmi, Jörg Epplen, Loïc Guillevin, David R. W. Jayne, Tao Jiang, Iva Gunnarsson, Peter Lamprecht, Stephen Leslie, Mark A. Little, Davide Martorana, Frank Moosig, Thomas Neumann, Sophie Ohlsson, Stefanie Quickert, Giuseppe A. Ramirez, Barbara Rewerska, Georg Schett, Renato A. Sinico, Wojciech Szczeklik, Vladimir Tesar, Damjan Vukcevic, The European Vasculitis Genetics Consortium, Benjamin Terrier, Richard A Watts, Augusto Vaglio, Julia U Holle, Chris Wallace, Kenneth G. C. Smith   +37 more
doaj   +1 more source

Epidemiology of Vasculitides in Khorasan Province, Iran

Iranian Journal of Medical Sciences, 2015
Vasculitides are a heterogeneous group of more than 20 diseases defined by inflammation and destruction of blood vessels. We aimed to study the demographic characteristics of the primary vasculitides in the North East of Iran.
Mohammadhassan Jokar, Zahra Mirfeizi
doaj  

Imaging signatures of eosinophilic granulomatosis with polyangiitis-related myocarditis: A case report. [PDF]

Radiol Case Rep
Lamassab NEH, Merimi I, Nabila I, Noha EO, Zakaria B.   +4 more
europepmc   +1 more source

Diagnosis and Treatment Pathway for Eosinophilic Granulomatosis with Polyangiitis in the Allergy Department. [PDF]

Diagnostics (Basel)
Liu J, Xu Y, Zhi Y.
europepmc   +1 more source