Results 231 to 240 of about 30,079 (265)

Granulomatosis with polyangiitis

Oral Surgery, 2014
AbstractGranulomatosis with polyangiitis (GPA), which was formerly known as Wegener's granulomatosis, is a rare systemic condition with oral manifestations. This case report describes and discusses the oral presentation, investigations, diagnosis and management options in a patient who was diagnosed with GPA.
P. Hoyle, J.C. Steele
openaire   +1 more source

From Head to Toe: Granulomatosis with Polyangiitis.

Radiographics, 2021
Granulomatosis with polyangiitis (GPA) is an antineutrophil cytoplasmic antibody-associated vasculitis. It is an uncommon multisystem disease involving predominantly small vessels and is characterized by granulomatous inflammation, pauci-immune ...
Mahatma I Guzman-Soto, Yukiyoshi Kimura, G. Romero-Sánchez, J. A. Cienfuegos-Alvear, F. Candanedo-Gonzalez, Yumi Kimura-Sandoval, D. Sanchez-Nava, Ingrid Alonso-Ramon, A. Hinojosa-Azaola   +8 more
semanticscholar   +1 more source

Two cases with new onset of ANCA-positive eosinophilic granulomatosis with polyangiitis under treatment with dupilumab: coincidence or causality?

Annals of the Rheumatic Diseases, 2022
We report two cases with new onset of myeloperoxidase-antineutrophil- cytoplasmic antibodies (MPO- ANCA)- positive eosinophilic granulomatosis with polyangiitis (EGPA) under treatment with dupilumab, a monoclonal antibody against IL- 4 and IL- 13 ...
M. von Deimling, Thomas C Koehler, B. Frye, E. Maerker-Hermann, N. Venhoff   +4 more
semanticscholar   +1 more source

Benralizumab as a steroid-sparing treatment option in eosinophilic granulomatosis with polyangiitis.

Journal of Allergy and Clinical Immunology: In Practice, 2020
BACKGROUND Eosinophilic granulomatosis with polyangiitis (EGPA) is a vasculitis associated with significant morbidity and mortality that has historically been treated with systemic corticosteroids and immunosuppressants.
V. Guntur, L. Manka, J. Denson, Ryan M. Dunn, Yeshai Dollin, M. Gill, C. Kolakowski, M. Strand, M. Wechsler   +8 more
semanticscholar   +1 more source

Eosinophilic Granulomatosis With Polyangiitis

JAMA Dermatology, 2021
Abraham M, Korman, Catherine G, Chung
openaire   +2 more sources

Sclerokeratitis in Granulomatosis with Polyangiitis

New England Journal of Medicine, 2022
Abigail, Jebaraj, Amy, Lin
openaire   +2 more sources

Granulomatosis with Polyangiitis

2018
Granulomatosis with polyangiitis (GPA), formerly Wegener’s granulomatosis, is a systemic vasculitis of unknown etiology affecting both small- and medium-sized arteries and veins. GPA manifests as necrotizing granulomatous inflammation in the lungs, kidneys, upper respiratory tract, nerves, and rarely heart.
J. Murphy, J. Ross, L. Coleman, M. Zakowski   +3 more
openaire   +1 more source

A Review of Anti-IL-5 Therapies for Eosinophilic Granulomatosis with Polyangiitis

Advances in Therapy, 2022
H. Koike, R. Nishi, Satoru Yagi, S. Furukawa, Yuki Fukami, M. Iijima, M. Katsuno   +6 more
semanticscholar   +1 more source

Granulomatosis with Polyangiitis

2019
Granulomatosis with polyangiitis (GPA) is a small-vessel necrotizing vasculitis that most characteristically affects the ear, nose, and throat (ENT), lungs, and/or kidneys. The median age at diagnosis is in the fifth decade, but children and older people can be affected.
openaire   +1 more source

At the Heart of Eosinophilic Granulomatosis with Polyangiitis: into Cardiac and Vascular Involvement

Current Rheumatology Reports, 2022
M. Bond, F. Fagni, M. Moretti, F. Bello, A. Egan, A. Vaglio, G. Emmi, C. Dejaco   +7 more
semanticscholar   +1 more source