Results 11 to 20 of about 5,556 (167)

Intracerebral Hemorrhage During the Chronic Phase of Eosinophilic Granulomatosis With Polyangiitis: A Case Report Emphasizing Cerebrovascular Vulnerability. [PDF]

Clin Case Rep
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of small‐vessel vasculitis typically associated with eosinophilia, asthma, and systemic inflammation. Although peripheral neuropathies are relatively common, central nervous system involvement, especially intracerebral hemorrhage during the remission phase of EGPA, is uncommon,
Watanabe S, Kasuya M, Shibata Y.
europepmc   +2 more sources

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

J Intern Med
Abstract Background Granulomatosis with polyangiitis (GPA) and eosinophilic granulomatosis with polyangiitis (EGPA) are distinct forms of antineutrophil cytoplasm antibody (ANCA)‐associated vasculitis (AAV). Increasing evidence suggests overlapping features, particularly in proteinase 3 (PR3)‐ANCA‐positive EGPA and GPA with eosinophilia.
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   +2 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

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

Eosinophilic Granulomatosis With Polyangiitis Presenting With Oral Granuloma as the Initial Symptom: A Case Report

Frontiers in Medicine, 2022
Antineutrophil cytoplasmic antibody associated vasculitis includes granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis (EGPA), and microscopic polyangiitis.
Lirong Lin, Rongjie Yu, Luquan Zheng, Shuyu Gong, Jurong Yang   +4 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

An atypical presentation of cardiac tamponade and periorbital swelling in a patient with eosinophilic granulomatosis with polyangiitis: a case report

Journal of Medical Case Reports, 2017
Background Eosinophilic granulomatosis with polyangiitis is a rare, necrotizing systemic vasculitis associated with asthma and hypereosinophilia. Its cause and pathophysiology are still being elucidated. Case presentation We report a case of eosinophilic
Alexandra C. Keefe, Joseph C. Hymas, Lyska L. Emerson, John J. Ryan   +3 more
doaj   +1 more source

Severe mononeuritis multiplex in a patient with eosinophilic granulomatosis with polyangiitis

Rheumatology, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterised by bronchial asthma, hypereosinophilia, and systemic vasculitis.
Desislava Kalinova, Georgi Kukushev, Zlatimir Kolarov, Rasho Rashkov   +3 more
doaj   +1 more source

Review of guideline for the management of ANCA-associated vasculitis, presented in 2021 by the American College of Rheumatology/Vasculitis Foundation

Научно-практическая ревматология, 2021
The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are a group of severe life-threatening autoimmune diseases, and one of the most important problems in practical rheumatology.
T. V. Beketova, I. Yu. Popov, V. V. Babak   +2 more
doaj   +1 more source