Results 71 to 80 of about 5,556 (167)

Chinese Guidelines for Diagnosis and Treatment of Chronic Rhinosinusitis (2024)

World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 12, Issue 1, Page 25-55, February 2026.
ABSTRACT Chronic rhinosinusitis (CRS), a complex inflammatory disease with heterogeneous pathogenesis, demands evolving evidence‐based strategies. Since the 2018 Chinese guidelines and EPOS2020, international advances in CRS immunopathology and biologics have revolutionized therapeutic approaches, particularly through phenotype–endotype classification ...
Subspecialty Group of Rhinology, Editorial Board of Chinese Journal of Otorhinolaryngology Head and Neck Surgery, Subspecialty Group of Rhinology, Society of Otorhinolaryngology Head and Neck Surgery, Chinese Medical Association   +4 more
wiley   +1 more source

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

Ischemic Stroke in Hypereosinophilic Syndrome: A Clinicopathologic Study of Two Cases

Neuropathology, Volume 46, Issue 1, February 2026.
ABSTRACT Ischemic stroke is a rare complication of hypereosinophilic syndrome (HES). Manifestations of stroke in HES have been described in the radiologic literature; however the pathologic characterization of central nervous system (CNS) involvement in HES is limited.
Karina C. Martin, Dan Straathof, Chi Lai, Harry V. Vinters   +3 more
wiley   +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

Familial Eosinophilic Granulomatosis with Polyangiitis

Open Journal of Rheumatology and Autoimmune Diseases, 2017
Eosinophilic granulomatosis with polyangiitis (EGPA) is an uncommon ANCA associated vasculitic disorder characterized by systemic necrotizing vasculitis of small vessels occurring exclusively among patients with bronchial asthma and tissue eosinophilia. Familial EGPA is extremely rare. Only two case reports have been published so far.
Abdurhman S. Al Arfaj, Mohammad Al Anazi, Najma Khalil, Akbar Ali Khan Pathan, Narsimha Reddy Parine   +4 more
openaire   +2 more sources

Never say never

Journal of Hospital Medicine, Volume 21, Issue 2, Page 200-204, February 2026.
Gurpreet Dhaliwal, Jagmeet Dhingra, Tom Fraser, Leal Herlitz, James Pile   +4 more
wiley   +1 more source

Eosinophilic Granulomatosis With Polyangiitis [PDF]

Chest, 2020
Alvise Berti, Divi Cornec, Marta Casal Moura, Robert J. Smyth, Lorenzo Dagna, Ulrich Specks, Karina A. Keogh   +6 more
openaire   +2 more sources

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

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

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