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A presentation of recurrent cerebral ischemic stroke in eosinophilic granulomatosis with polyangiitis: a case report [PDF]
Journal of Medical Case ReportsBackground Eosinophilic granulomatosis with polyangiitis is characterized as a small vessel vasculitis with the propensity to have a myriad of presentations due to the targeting of several different organ systems. More often than not, it is the pulmonary
Bryan Gregory +6 more
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Eosinophilic Cholecystitis Associated with Eosinophilic Granulomatosis with Polyangiitis [PDF]
Case Reports in Gastroenterology, 2020 We report a case of eosinophilic cholecystitis associated with eosinophilic granulomatosis with polyangiitis (EGPA) complicated by cerebral hemorrhage.
Hiroyuki Ito +13 more
doaj +3 more sources
Eosinophilic granulomatosis with polyangiitis: an overview [PDF]
Frontiers in Immunology, 2014 Eosinophilic granulomatosis with polyangiitis (EGPA) is a multisystemic disorder, belonging to the small vessel ANCA-associated vasculitis, defined as a eosinophil-rich and necrotizing granulomatous inflammation often involving the respiratory tract, and
Andrea eGioffredi +3 more
doaj +3 more sources
An overlap of granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis
Saudi Journal of Kidney Diseases and Transplantation, 2017 We present a case report of overlap of granulomatosis with polyangiitis (GPA; formerly known as Wegener’s granulomatosis) and eosinophilic granulomatosis with polyangiitis (EGPA; formerly known as Churg-Strauss syndrome).
Sujit Surendran +4 more
doaj +3 more sources
Eosinophilic Granulomatosis with Polyangiitis
New England Journal of Medicine, 2022 A 42-year-old man presented with red, painful eyes, facial-nerve palsy on the left side, a large oral ulcer, and petechiae. Tests for antibodies against perinuclear antineutrophil cytoplasmic antibody and proteinase 3 were positive. Skin biopsy revealed leukocytoclastic vasculitis with perivascular eosinophils.
Geng-Yi Yong, Amelia L.-S. Lim
+11 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 ...
Shunsuke Furuta +2 more
doaj +3 more sources
Prevasculitic Eosinophilic Granulomatosis With Polyangiitis [PDF]
Cureus, 2021 Eosinophilic granulomatosis with polyangiitis (EGPA) is an exceptionally rare systemic necrotizing vasculitis. The disease is clinically characterized by asthma with concomitant blood and tissue eosinophilia, often progressing to eosinophilic vasculitis. From the onset of asthma, there is usually a three to nine year delay of EGPA diagnosis.
Burtson, Kathryn M, Bishop, Jonathan
openaire +2 more sources
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 +3 more
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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 +3 more
+6 more sources
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 +3 more
doaj +1 more source