Results 151 to 160 of about 64,509,941 (193)

Case Report: Severe ANCA-positive eosinophilic granulomatosis with polyangiitis presenting with Loeffler endocarditis and cryofibrinogenemia-associated digital gangrene successfully treated with rituximab. [PDF]

Front Immunol
Ostric Pavlovic I, Trifunovic-Zamaklar D, Bonaci-Nikolic B, Bascarevic M, Tomic-Spiric V, Peric-Popadic A, Dragasevic Miskovic N, Ukropina B, Reljic A, Kusic N, Pavlovic A, Velickovic A, Radovic S, Arandjelovic S.   +13 more
europepmc   +1 more source

Correction to "Kimura Disease With Eosinophilic Granulomatosis With Polyangiitis Successfully Treated by Mepolizumab". [PDF]

Clin Case Rep
europepmc   +1 more source

Dual pathogenesis and treatment approaches for eosinophilic granulomatosis with polyangiitis: a comprehensive review. [PDF]

Reumatologia
Kosałka-Węgiel J, Sebastian A.
europepmc   +1 more source

Airway immune profiles and therapeutic implications of IGF1 in eosinophilic granulomatosis with polyangiitis. [PDF]

Nat Commun
Dong C, Lu B, Zhong C, Ou C, Yang X, Wang L, Zuo X, Xue L, Lu C, Wang S, Wen J, Ma J, Deng Z, Liu Y, Ma L, Liu M, Lew AM, Mukherjee M, Nair P, Zhong N, Chen R, Chen Z, Zhang Y, Zhang Q.   +23 more
europepmc   +1 more source

Case Report: Angioimmunoblastic T-cell lymphoma initially diagnosed as eosinophilic granulomatosis with polyangiitis. [PDF]

Front Med (Lausanne)
Ni Y, Sun Y, Xie S, Xie J, Shi G, Dai R, Guo Y.   +6 more
europepmc   +1 more source

Eosinophilic Granulomatosis With Polyangiitis (EGPA) Manifesting as Giant Cell Arteritis After Initiating Treatment With Dupilumab: An Unusual Clinical Presentation. [PDF]

Cureus
Zafar S, Medina E, Panesar R, Murthy VL.
europepmc   +1 more source

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Eosinophilic granulomatosis with polyangiitis

Medicina Clínica (English Edition), 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterized by the presence of asthma associated with eosinophilia, eosinophilic infiltration of different organs, and vasculitis of small and medium-sized vessels. Although classified as anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, it occurs in less ...
Carlos, Romero Gómez, Halbert, Hernández Negrín, María Del Mar, Ayala Gutiérrez   +2 more
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Eosinophilic granulomatosis with polyangiitis: A review

Autoimmunity Reviews, 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare, multi-system, inflammatory disease, belonging to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV). Previously known as Churg-Strauss syndrome, EGPA is characterised by late-onset asthma, eosinophilia and vasculitis affecting small-to-medium vessels ...
Shirish Dubey
exaly   +3 more sources