Results 11 to 20 of about 9,401 (207)

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 ...
Jpe, White, S, Dubey
openaire   +4 more sources

Mepolizumab or placebo for eosinophilic granulomatosis with polyangiitis [PDF]

New England Journal of Medicine, 2017
Background Eosinophilic granulomatosis with polyangiitis is an eosinophilic vasculitis. Mepolizumab, an anti–interleukin-5 monoclonal antibody, reduces blood eosinophil counts and may have value in the treatment of eosinophilic granulomatosis with ...
Akuthota, Praveen, Andrea Matucci, Andrew Wardlaw, Anoop Chauhan, Antoine G Sreih, Arnaud Bourdin, Aryeh Fischer, Benjamin A Raby, Berhnard Hellmich, Bertrand Dunogue, Brown, Judith, Bruce Bochner, Chiara Baldini, Christian Pagnoux, Christof Iking-Konert, Cid, Maria C, Curry L Koening, Douglas M Beach, Elide Pastorello, Florence Roufosse, Georgina Espígol-Frigolé, Gerald J, Gleich, Jan Schirmer, Jayne, David, Jean-Emmanuel Kahn, José Hernández-Rodríguez, Joshua Denson, Julia Holle, Khoury, Paneez, Klion, Amy, Langford, Carol A, Lindsay Morehouse, Luqmani, Raashid, Mallett, Stephen, Maria Grazia Sabbadini, Masami Taniguchi, Merkel, Peter A, Moosig, Frank, Nader Khalidi, Pascal Chanez, Paul Monach, Peter Kern, Philipson, Richard, Reinhard Voll, Rula Hajj-Ali, Ryan M Dunn, Ryann Murphy, Sergio Prieto-González, Specks, Ulrich, Steinfeld, Jonathan, Thomas Neumann, Tomonori Ishii, Vincent Cottin, Wechsler, Michael E, Weller, Peter F, Xavier Puechal, Yancey, Steve W, Yeshai Dollin   +58 more
core   +4 more sources

Overlapping forms of granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis: Insights from a European multicenter study. [PDF]

J Intern Med
Background Granulomatosis with polyangiitis (GPA) and eosinophilic granulomatosis with polyangiitis (EGPA) are distinct forms of antineutrophil cytoplasm antibody (ANCA)‐associated vasculitis (AAV).
Pallotti F, Mettler C, Papo M, Iudici M, Padoan R, Sorin B, Regola F, Franceschini F, Moiseev S, Novikov P, Piga MA, Moroncini G, Brix SR, Kafagi AH, Deshayes S, Aouba A, Campagne J, Delvino P, Tervaert JWC, Brussino L, Michaud M, Venhoff N, Alberici F, Iannone C, Rosenstingl S, Moutel M, Galempoix JM, Cottin V, Jaccard C, Riehl D, Legendre P, Billet AC, Parronchi P, Quartuccio L, Teixeira V, Egan A, Jayne D, Tombetti E, Caminati M, Pagnoux C, Regent A, Ruivard M, Guillevin L, Puéchal X, Terrier B, French Vasculitis Study Group (FVSG).   +45 more
europepmc   +3 more sources

Eosinophilic Granulomatosis with Polyangiitis

, 2018
Eosinophilic granulomatosis with polyangiitis (EGPA) formerly Churg-Strauss syndrome is an autoimmune disease of small vessel vasculitis characterized by eosinophilic granulomatosis that manifests as asthma, eosinophilia, granuloma formation, and eventual systemic vasculitis.
M. Zakowski, J. Murphy, J. Ross, L. Coleman   +3 more
  +6 more sources

Eosinophilic granulomatosis with polyangiitis (Churg–Strauss syndrome) imitating Guillain–Barre syndrome (GBS): a case report

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2021
Background Eosinophilic granulomatosis with polyangiitis (EGPA) is associated with vasculitic neuropathy and being rare can present as subacute symmetric sensorimotor quadriparesis mimicking Guillain–Barre syndrome (GBS).
Dinesh Khandelwal, Mridula Singh, Ruchi Jagota, Vaibhav Mathur   +3 more
doaj   +1 more source

Characterizing infection in anti-neutrophil cytoplasmic antibody-associated vasculitis:results from a longitudinal, matched-cohort data linkage study [PDF]

, 2020
Objectives: Infection exerts a major burden in ANCA-associated vasculitis (AAV), however, its precise extent and nature remains unclear. In this national study we aimed to longitudinally quantify, characterize and contextualize infection risk in AAV ...
Amft, Nicole, Basu, Neil, Black, Corri, Dhaun, Neeraj, Erwig, Lars, Harvie, John, Kumar, Vinod, Marks, Angharad, McGeoch, Lucy, McLaren, John, Sarica, Shifa H., Sznajd, Jan   +11 more
core   +6 more sources

Acute exacerbation of idiopathic hypereosinophilic syndrome following asymptomatic coronavirus disease 2019: a case report

Journal of Medical Case Reports, 2022
Background Previous research has suggested that some autoimmune diseases develop after the occurrence of coronavirus disease 2019. Hypereosinophilic syndrome is a rare disease presenting with idiopathic eosinophilia and multiple organ involvement ...
Satoshi Suzuki, Keiko Suzuki, Takaya Ichikawa, Kae Takahashi, Masako Minami-Hori, Yoko Tanino   +5 more
doaj   +1 more source

Eosinophilic granulomatosis with polyangiitis: sequential use of mepolizumab following rituximab for inadequate asthma control despite vasculitis remission

Reumatismo, 2023
We report the case of a 54-year-old woman with antineutrophilic cytoplasmic antibody-negative eosinophilic granulomatosis with polyangiitis presenting with mononeuritis multiplex, intestinal hemorrhage, cardiomyopathy, fever, and worsening asthma ...
B. Cremonezi Lammoglia, L. de Aguiar Trevise, T. Paslar Leal, M. Pereira Lopes Vieira Pinto, G. Hasselmann, N. Salles Rosa Neto   +5 more
doaj   +1 more source

The role of the host—Neutrophil biology

Periodontology 2000, EarlyView., 2023
Abstract Neutrophilic polymorphonuclear leukocytes (neutrophils) are myeloid cells packed with lysosomal granules (hence also called granulocytes) that contain a formidable antimicrobial arsenal. They are terminally differentiated cells that play a critical role in acute and chronic inflammation, as well as in the resolution of inflammation and wound ...
Iain L. C. Chapple, Josefine Hirschfeld, Alpdogan Kantarci, Asaf Wilensky, Lior Shapira   +4 more
wiley   +1 more source

Colitis as the Initial Presentation of Eosinophilic Granulomatosis with Polyangiitis

Case Reports in Rheumatology, 2023
A male patient in his early sixties with recurrent diarrhea was transferred to our hospital. The patient did not have any pulmonary or upper respiratory symptoms. He was noted to have peripheral eosinophilia.
Sharika Gopakumar Menon, Steven Hugenberg, Ahmad M. Alkashash, Jingmei Lin, Arya M. Iranmanesh   +4 more
doaj   +1 more source