Results 1 to 10 of about 6,209 (117)

Genetic associations of eosinophilic granulomatosis with polyangiitis in the Japanese population: exploring similarities and differences with European populations [PDF]

open access: yesRMD Open
Objectives Eosinophilic granulomatosis with polyangiitis (EGPA) is classified as a subtype of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).
Takayuki Sumida   +28 more
doaj   +2 more sources

Case Report: From misdiagnosis to successful treatment using mepolizumab in ANCA-negative severe EGPA—clinical lessons in eosinophil-targeted therapy [PDF]

open access: yesFrontiers in Medicine
This paper presents the complex diagnostic course and treatment of a 33-year-old female patient with anti-neutrophil cytoplasmic antibodies (ANCA)-negative eosinophilic granulomatosis with polyangiitis (EGPA).
Ju-Zhang Li   +3 more
doaj   +2 more sources

Identification of a diagnostic metabolomic fingerprint in plasma for eosinophilic granulomatosis with polyangiitis. [PDF]

open access: yesPLoS ONE
ObjectiveEosinophilic granulomatosis with polyangiitis (EGPA) was a rare systemic vasculitis characterized by eosinophilia, asthma, and necrotizing vasculitis.
Songsen Su, Yanfang Lin
doaj   +2 more sources

Distinct features of hypereosinophilic syndrome with neuropathy from eosinophilic granulomatosis with polyangiitis

open access: yesFrontiers in Neurology, 2022
Background and objectivesHypereosinophilic syndrome (HES) and eosinophilic granulomatosis with polyangiitis (EGPA) have overlapping clinical considerations, which frequently involve peripheral neuropathy.
Hiroki Takeuchi   +4 more
doaj   +1 more source

Effective treatment with mepolizumab in a patient with severe eosinophilic granulomatosis with polyangiitis complicated with small intestine perforation

open access: yesRespiratory Medicine Case Reports, 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is systemic vasculitis caused by eosinophilia affecting small to medium-sized blood vessels, which damages the organs.
Mari Sato   +17 more
doaj   +1 more source

Gut Microbiota and Associated Mucosal Immune Response in Eosinophilic Granulomatosis with Polyangiitis (EGPA)

open access: yesBiomedicines, 2022
Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. A genome-wide association study showed a correlation between ANCA-negative EGPA and variants of genes encoding proteins with ...
Elena Niccolai   +14 more
doaj   +1 more source

Computed tomography findings of paranasal sinuses in patients with eosinophilic granulomatosis with polyangiitis: Comparison with other eosinophilic sinus diseases and clinical relevance of their severity

open access: yesAllergology International, 2023
Background: Although paranasal sinuses are one of the most representative organs affected by eosinophilic granulomatosis with polyangiitis (EGPA), they have not been studied sufficiently.
Maki Iwata   +8 more
doaj   +1 more source

Eosinophilic granulomatosis polyangiitis (EGPA) complicated with periaortitis, precipitating role of dupilumab? A case report a review of the literature

open access: yesRMD Open, 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is an ANCA-associated vasculitis that affects small size vessels. Only four cases of periaortitis associated with EGPA have been reported in the literature.
Patrice Cacoub   +5 more
doaj   +1 more source

Serum Proteomic Analysis Identifies SAA1, FGA, SAP, and CETP as New Biomarkers for Eosinophilic Granulomatosis With Polyangiitis

open access: yesFrontiers in Immunology, 2022
BackgroundEosinophilic granulomatosis with polyangiitis (EGPA) is characterized by asthma-like attacks in its early stage, which is easily misdiagnosed as severe asthma. Therefore, new biomarkers for the early diagnosis of EGPA are needed, especially for
Jing Xiao   +15 more
doaj   +1 more source

Symposium 10: Spotting EGPA from Asthma Populations and How Co-Care Works Between Rheumatology and Respiratory Physicians: A Case Sharing

open access: yesJournal of Clinical Rheumatology and Immunology, 2023
Eosinophilic Granulomatosis with Polyangiitis (EGPA), formerly known as Churg-Strauss syndrome, is a rare systemic vasculitis characterized by asthma, eosinophilia, and vasculitic organ involvement.
Ping-Hung KUO
doaj   +1 more source

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