Results 91 to 100 of about 67,511,782 (172)

Eosinophilic granulomatosis with polyangiitis: an overview

Frontiers in Immunology, 2014
Eosinophilic granulomatosis with polyangiitis (EGPA) is a multisystemic disorder, belonging to the small vessel ANCA-associated vasculitis, defined as a eosinophil-rich and necrotizing granulomatous inflammation often involving the respiratory tract, and
Andrea eGioffredi, Federica eMaritati, Elena eOliva, Carlo eBuzio   +3 more
doaj   +1 more source

Combination Biologic Therapy with Mepolizumab and Dupilumab for Severe Eosinophilic Granulomatosis with Polyangiitis and Chronic Rhinosinusitis with Nasal Polyp [PDF]

We report the case of a 55-year-old female with eosinophilic granulomatosis with polyangiitis and chronic rhinosinusitis with nasal polyp. Rhinosinusitis recurred 6 months after full-house endoscopic sinus surgery.
竹内,裕美, Takeuchi,Hiromi, Fujiwara,Kazunori, タケウチ,ヒロミ, ナカムラ,ヨウスケ, フジワラ,カズノリ, 中村,陽祐, Nakamura,Yosuke, Kimura,Toru, Kikumoto,Naoki, Nakamori,Motoki, 藤原,和典   +11 more
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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

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

FCGR3B polymorphism predicts relapse risk in eosinophilic granulomatosis with polyangiitis

, 2020
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare disease included in the spectrum of ANCA-associated vasculitis, although ANCA (usually anti-MPO, MPO ANCA) are positive in only ∼40% of patients.
Sinico, Renato A, Fenaroli, Paride, Adorni, Alessia, Daminelli, Giulia, Urban, Maria Letizia, Martorana, Davide, Maritati, Federica, Vaglio, Augusto, Peyronel, Francesco, Palmisano, Alessandra, Alberici, Federico, Bonatti, Francesco, Percesepe, Antonio, Emmi, Giacomo, Marvisi, Chiara, Gregorini, Gina   +15 more
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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

Eosinophilic Variant of Orbital Granulomatosis with Polyangiitis with Hyperimmunoglobulinemia E: A Case Report

, 2018
The eosinophilic variant of granulomatosis with polyangiitis (GPA) is rare condition with unknown etiology. To describe a patient with limited orbital GPA who had significant eosinophilia and hyperimmunoglobulinemia E (hyper-IgE)
Ji Eun Lee
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Is there a role for imatinib mesylate in the treatment of eosinophilic granulomatosis with polyangiitis?

, 2015
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic eosinophilic vasculitis, belonging to the group of ANCA-associated vasculitides (AAV).
Cuccuru, Luciana, Passiu, Giuseppe, Erre, Gian Luca, Pardini, Simonetta, Taras, Loredana   +4 more
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Clinical case of favourable outcome at a patient with eosinophilic granulomatosis with polyangiitis complicated by severe heart disease [PDF]

, 2018
The aim of the article is to present a clinical case of rapid generalization of eosinophilic granulomatosis with polyangiitis. The course of disease with multiple organ lesions and the heart being affected the most is described.
Romanova I.A., Alexandrova O.L., Alexandrova N.L., Skryabina E.N., Nikitina N.M.   +4 more
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Concurrent CRAO with Arteritic AION in Eosinophilic Granulomatosis with Polyangiitis

, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic necrotizing vasculitis characterized by peripheral neuropathy, pulmonary involvement, and eosinophilia. EGPA has been associated with a number of ocular conditions, including retinal
Anuchit Poonyathalang; Tanyatuth Padungkiatsagul; Kavin Vanikieti; Thitiporn Thongborisuth
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