Results 91 to 100 of about 12,403 (234)

Idiopathic Eosinophilic Pneumonia with Associated Pulmonary Vasculitis in Horse: A Case Series [PDF]

, 2016
Various eosinophilic lesions and their association with diseases have been described in horses. Multisystemic Eosinophilic Epitheliotropic Disease (MEED) characterized by eosinophilic granulomas in various organs represent the most diffuse manifestation.
Magi, Gian Enrico, Mari, Subeide, Mariotti, Francesca, Rossi, Giacomo   +3 more
core   +1 more source

ANCA-associated vasculitis in childhood: recent advances

Italian Journal of Pediatrics, 2017
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides are rare systemic diseases that usually occur in adulthood. They comprise granulomatosis with polyangiitis (GPA, Wegener’s), microscopic polyangiitis (MPA) and eosinophilic ...
Marta Calatroni, Elena Oliva, Davide Gianfreda, Gina Gregorini, Marco Allinovi, Giuseppe A. Ramirez, Enrica P. Bozzolo, Sara Monti, Claudia Bracaglia, Giulia Marucci, Monica Bodria, Renato A. Sinico, Federico Pieruzzi, Gabriella Moroni, Serena Pastore, Giacomo Emmi, Pasquale Esposito, Mariagrazia Catanoso, Giancarlo Barbano, Alice Bonanni, Augusto Vaglio   +20 more
doaj   +1 more source

Natural Killer Cells in Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - A Review of the Literature

Frontiers in Immunology, 2022
Anti-neutrophil cytoplasmic antibody (ANCA)- associated vasculitis (AAV) is a group of systemic autoimmune diseases characterized by inflammation of small- and medium-sized vessels.
Sina Fuchs, Andrea Scheffschick, Iva Gunnarsson, Iva Gunnarsson, Hanna Brauner, Hanna Brauner   +5 more
doaj   +1 more source

Mepolizumab and benralizumab in patients with severe asthma and a history of eosinophilic granulomatosis with polyangiitis

Frontiers in Medicine
Introduction Asthma associated with eosinophilic granulomatosis with polyangiitis (EGPA) is often severe and corticosteroid-dependent, leading to significant morbidity.
C. Desaintjean, K. Ahmad, J. Traclet, M. Gerfaud-Valentin, C. Durel, J. Glérant, A. Hot, F. Lestelle, Sabine Mainbourg, M. Nasser, P. Sève, S. Turquier, G. Devouassoux, V. Cottin   +13 more
semanticscholar   +1 more source

New-onset severe eosinophilic granulomatosis with polyangiitis following the third dose of mRNA COVID-19 vaccine: A case report.

Modern Rheumatology Case Reports, 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is a complex multifactorial disease that results in multisystemic inflammation of the small- and medium-sized arteries.
Salah Mahdi, Anwar I. Joudeh, Krishnamoorthy Sundara Raman, Samia Ait Faqih, Mohammed Alhatou, M. F. Wadiwala, Mohammed Akhtar, Abdo Lutf   +7 more
semanticscholar   +1 more source

Incidence, Prevalence, and Mortality of Eosinophilic Granulomatosis With Polyangiitis in Korea: A Nationwide Population-Based Study

Allergy Asthma and Immunology Research
Purpose Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of vasculitis with multiorgan involvement. The incidence and prevalence of EGPA vary geographically and ethnically.
Ji-ho Lee, Sewoon Hong, Iseul Yu, Min-Seok Chang, Sunmin Park, Seok Jeong Lee, Sang-Ha Kim   +6 more
semanticscholar   +1 more source

Characteristics of Severe Asthma Clinic Patients with Eosinophilic Granulomatosis with Polyangiitis.

Journal of Allergy and Clinical Immunology: In Practice
BACKGROUND Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis associated with varying clinical presentations and overlapping multiorgan involvement.
Youxin Puan, K. Y. Ong, P. Y. Tiew, Gabriel Chen, N. Teo, Andrea Hsiu Ling Low, Michael E Wechsler, M. Koh   +7 more
semanticscholar   +1 more source

Impaired function of endothelial progenitor cells in children with primary systemic vasculitis [PDF]

, 2015
INTRODUCTION: Previously, we demonstrated that children with active systemic vasculitis (SV) have higher circulating CD34 + CD133 + KDR+ endothelial progenitor cells (EPC); the function of these EPCs, and their relationship with disease activity in ...
Brogan, PA, Eleftheriou, D, Hong, Y, Klein, NJ   +3 more
core   +1 more source

Aspergillosis myocarditis in the immunocompromised host

IDCases, 2019
Invasive cardiac aspergillosis has been rarely described in immunocompromised patients. This disease is difficult to diagnose by conventional laboratory, microbiologic, and imaging techniques, and is often recognized only post-mortem. The authors present
Sean S. Bullis, Alison Krywanczyk, Andrew J. Hale   +2 more
doaj   +1 more source

Psoriasis‐like skin rash triggered by a local infection in a patient with eosinophilic granulomatosis with polyangiitis that was well controlled by mepolizumab treatment

Clinical Case Reports, 2023
Key Clinical message A patient with eosinophilic granulomatosis with polyangiitis, who was well‐controlled by pharmacotherapy, developed a psoriasis‐like rash due to a local infection. It represents the consequence of an immunologic imbalance. Abstract A
Naho Yokota, Makoto Kondo, Akinobu Hayashi, Masako Ichishi, Yoshiaki Matsushima, Takehisa Nakanishi, Koji Habe, Keiichi Yamanaka   +7 more
doaj   +1 more source