Results 81 to 90 of about 8,274 (166)

A Case of Eosinophilic Granulomatosis With Polyangiitis Presenting With Conjunctival Lesions During Treatment With IL-5 Inhibitors

Case Reports in Rheumatology
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic rheumatic disease characterized by necrotizing vasculitis in the small vessels with eosinophilic inflammation.
Shin-Ichiro Ohmura, Soma Fukami, Kazuhisa Uemura, Yoshiro Otsuki   +3 more
doaj   +1 more source

135. ATHERO-THROMBOTIC AND VENOUS EVENTS (AVTE) IN EOSINOPHILIC GRANULOMATOSIS WITH POLYANGIITIS (EGPA): A MULTICENTRE STUDY OF 573 ITALIAN PATIENTS

, 2019
Background:Eosinophilic Granulomatosis with Polyangiitis (EGPA)belongs to the spectrum of ANCA- associated vasculitis. There isgrowing evidence that systemic inflammatory diseases are associatedwith increased risk of both atherothrombotic (coronary ...
Sinico, Renato, Schiavon, Franco, Vaglio, Augusto, Prisco, Domenico, Bettiol, Alessandra, Emmi, Giacomo, Urban, Maria Letizia, Caporali, Roberto   +7 more
core   +1 more source

Pituitary dysfunction with eosinophilic granulomatosis with polyangiitis presenting with diabetes insipidus: a case report and review of the literature

Frontiers in Immunology
Central diabetes insipidus secondary to hypophysitis in eosinophilic granulomatosis with polyangiitis (EGPA) is very rare, and this article summarizes one case reported from our site as well as two previously reported patients with EGPA, both of whom had
Aifei Zhang, Xiaoxia Liu, Pengjia Wu, Longyan Qin, Na Li, Yi Yin, Jiashun Zeng   +6 more
doaj   +1 more source

Unveiling the Unseen Signals: Identifying Novel Diagnostic and Prognostic Biomarkers for Eosinophilic Granulomatosis with Polyangiitis

reservedBackground Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis characterized by necrotizing inflammation of small to medium-sized blood vessels.
IORIO, LUCA
core  

Serum biomarkers of patients with EGPA based on use of immunosuppressive agents at time of study visit.

, 2015
Data are shown as median (range in parenthesis); EGPA: eosinophilic granulomatosis with polyangiitis (Churg-Strauss); immunosuppr., immunosuppressive agents (9 patients were on methotrexate, 7 on azathioprine and 1 on mycophenolate mofetil); LR, Logistic
David Cuthbertson (188652), Peter A. Merkel (188721), Simon Carette (188665), Bastian Oppl (713196), Christian Dejaco (12618), Nader Khalidi (713199), Gary Hoffman (713198), Paul Monach (713197), Jochen Zwerina (11574), Carol Langford (713201), Steven Ytterberg (713203), Curry Koening (713200), Philip Seo (188695), Ulrich Specks (972), Kathleen McKinnon-Maksimowicz (713202)   +14 more
core   +1 more source

Acute aortoiliac thrombosis and mitral valve regurgitation as acute onset of Eosinophilic Granulomatosis with Polyangiitis (EGPA) in a 26-year-old patient [PDF]

We present a rare case of Eosinophilic Granulomatosis with Polyangiitis (EGPA), involving a 26-year-old woman with a history of asthma and nasal polyps.
Luca Galassi, MD, Davide Passolunghi, MD, Passolunghi, Davide, Giulia Lerva, Davide Passolunghi, Maria Rosa Pozzi, Valerio Stefano Tolva, MD, PhD, Giovanni Marchetto, MD, Pozzi, Maria Rosa, Giovanni Marchetto, Galassi, Luca, Valerio Stefano Tolva, Lerva, Giulia, Marchetto, Giovanni, Tolva, Valerio Stefano, Luca Galassi, Maria Rosa Pozzi, MD, Giulia Lerva, MD   +17 more
core   +1 more source

Transient Eosinophilic Granulomatosis with Polyangiitis-Like Vasculitis During Omalizumab Therapy: A Case Report

Open Access Rheumatology: Research and Reviews, 2020
Sara Elhadari, Mahir Hamad Acute Medicine Department, The James Cook University Hospital, Middlesbrough, TS4 3BW, UKCorrespondence: Sara Elhadari Email sara.elhadari@nhs.netAbstract: A 67-year-old Caucasian female presented in August 2019 to our ...
Elhadari S, Hamad M
doaj  

Bericht über die EGPA Jahreskonferenz 2017 in Mailand: Permanent Study Group «Justice and Court Administration»

, 2017
Ende August 2017 fand im Rahmen der Konferenz der European Group for Public Administration (EGPA) in Mailand das jährliche Meeting der Permanent Study Group „Justice and Court Administration“ statt.
Schmied, Martin
core  

Switching from multiple-inhaler triple therapy to single, extra fine-inhaler triple therapy in severe refractory asthma with EGPA: beyond control. Case report and review of the literature

Drugs in Context
Eosinophilic granulomatosis with polyangiitis is a rare systemic vasculitis associated with asthma, eosinophilia and multi-organ involvement. This case report describes a 69-year-old male with severe, poorly controlled asthma who was diagnosed with ...
Francesco Menzella, Marcello Cottini, Silvia Tonin, Lorenzo Corsi, Annamaria Bosi, Andrea Ballarin, Ariel Floriani, Cristina Dartora, Matteo Tacconi, Carlo Lombardi   +9 more
doaj   +1 more source

Comparative Insights on IL-5 Targeting with Mepolizumab and Benralizumab: Enhancing EGPA Treatment Strategies

Eosinophilic granulomatosis with polyangiitis (EGPA) is a necrotizing vasculitis characterized by extravascular granulomas and eosinophilia in both blood and tissues.
Ryuhei Ishihara, Ryu Watanabe, Mayu Shiomi, Takashi Nakazawa, Motomu Hashimoto, Sayaka Tanaka   +5 more
core   +1 more source