Results 1 to 10 of about 67,511,782 (172)

Wells’ syndrome associated with eosinophilic granulomatosis with polyangiitis − A case report [PDF]

Vojnosanitetski Pregled, 2021
Introduction. Wells` syndrome (eosinophilic cellulitis) is a chronic, recurrent disease characterized by episodes of erythematous and edematous plaques or nodules with occasional development of hemorrhagic bullae on the trunk and limbs.
Radević Tatjana, Kandolf-Sekulović Lidija, Ristić Gorica G., Mijušković Željko P.   +3 more
doaj   +2 more sources

Colitis as the Initial Presentation of Eosinophilic Granulomatosis with Polyangiitis [PDF]

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   +2 more sources

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   +2 more sources

Update on eosinophilic granulomatosis with polyangiitis

Allergology International, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) (formerly Churg-Strauss syndrome) is a rare form of anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis characterized by eosinophil-rich granulomatous inflammation and small to medium-size ...
Hiroshi Nakajima, Shunsuke Furuta, Taro Iwamoto   +2 more
exaly   +3 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

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

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

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