Results 21 to 30 of about 12,403 (234)

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

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

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

Eosinophilic granulomatosis with polyangiitis (EGPA) and PRES: a case-based review of literature in ANCA-associated vasculitides [PDF]

, 2015
Eosinophilic granulomatosis with polyangiitis (EGPA) is a small-sized vessel systemic necrotizing vasculitis and belongs to the family of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides.
Barilaro, Giuseppe, Granata, Massimo, Marra, ALESSANDRO MARIA, Villella, Valeria   +3 more
core   +1 more source

An uncommon presentation of eosinophilic granulomatosis with polyangiitis: a case report [PDF]

, 2014
INTRODUCTION: Eosinophilic granulomatosis with polyangiitis is a rare and potentially fatal disease if not readily diagnosed. Cerebral involvement is extremely rare and clinical presentation as hemorrhagic stroke is even rarer.
Andolina, G, Banco, MA, Bonura, A, BUSCEMI, Silvio, COSTANZA GAGLIO, Edy, TAORMINA, Giuseppe   +5 more
core   +2 more sources

T Cells in Vascular Inflammatory Diseases [PDF]

, 2014
Inflammation of the human vasculature is a manifestation of many different diseases ranging from systemic autoimmune diseases to chronic inflammatory diseases, in which multiple types of immune cells are involved. For both autoimmune diseases and chronic
Abdulahad, Abdulahad, Abdulahad, Abdulahad, Abdulahad, Abdulahad, Ait-Oufella, Ait-Oufella, Allez, Almanzar, Ammirati, Appay, Bauer, Beeton, Beeton, Beeton, Bettelli, Brouwer, Brouwer, Brown, Cahalan, Capraru, Caruso, Chandy, Chavele, Cohen Tervaert, Davenport, de Boer, de Boer, de Leeuw, de Menthon, Deng, Ebert, Elhage, Erbel, Erbel, Ettinger, Fazilleau, Fontenot, Free, Frostegard, Gan, Gao, Gao, Gephardt, Geri, Gocke, Gotsman, Groh, Gupta, Hauer, Hoshino, Hoshino, Hu, Huber, Imura, Ivanov, Jennette, Jennette, Jonasson, Jonasson, Jovanovic, Kallenberg, Karnell, Kellner, King, King, Kjellev, Klapa, Koch Hansen, Koenen, Komocsi, Laan, Lamprecht, Lamprecht, Langford, Lee, Liston, Lockwood, Mallat, Mallat, Mangan, Matheu, Mestas, Moosig, Morgan, Muller, Niebuhr, Nogueira, Odobasic, Ogasawara, Ooi, Ordonez, Panettieri, Popa, Roselaar, Ruth, Saadoun, Saito, Saito, Samson, Samson, Sanders, Schmitt, Schmitt, Schonermarck, Seta, Smith, Stegeman, Stegeman, Taleb, Terrier, Tse, Valencia, van Es, van Loosdregt, Vincenti, Wang, Weidner, Whitman, Whitman, Whitman, Wilde, Wulff, Xia, Zhou, Zhou, Zhou, Zielinski   +128 more
core   +7 more sources