Zobrazeno 1 - 10
of 3 893
pro vyhledávání: '"wegener's granulomatosis"'
Autor:
Salaheldin Awouda, Gustavo Andres Grimaldi Finol, Enas Mohammed, Malaz Adam, Moustafa Al Khalil
Publikováno v:
Oral and Maxillofacial Surgery Cases, Vol 10, Iss 3, Pp 100363- (2024)
Granulomatosis with Polyangiitis previously called Wegener's granulomatosis is quite a rare condition that affects multiple organs. It's a serious disorder marked by inflammation that causes tissue damage in the upper and lower respiratory tract, glo
Externí odkaz:
https://doaj.org/article/b5856bf22c8740f395d5777a16b89233
Publikováno v:
Clinical Dermatology Review, Vol 8, Iss 2, Pp 134-137 (2024)
Wegener's Granulomatosis with polyangiitis (GPA) is a systemic disease of unknown etiology characterized by necrotizing granulomatous inflammation, tissue necrosis, and variable degrees of vasculitis in small- and medium-sized blood vessels. The clas
Externí odkaz:
https://doaj.org/article/2885cac5a2f84ce59105b1fa8b47ffce
Publikováno v:
Medicina, Vol 60, Iss 10, p 1690 (2024)
Background: Ocular involvement is relatively common in granulomatosis with polyangiitis (GPA); however, choroidal involvement is rare. We present a case of serous retinal detachment resulting from choroidal involvement in GPA. Case presentation: A 55
Externí odkaz:
https://doaj.org/article/4f3eeee198a3475da2a33791698f669e
Publikováno v:
Radiology Case Reports, Vol 18, Iss 10, Pp 3704-3709 (2023)
To share a unique case of granulomatosis with polyangiitis (GPA) identified in a child with CNS involvement, specifically PRES (posterior reversible encephalopathy syndrome). Discuss this uncommon manifestation's clinical characteristics, diagnostic
Externí odkaz:
https://doaj.org/article/c90412f1ee5c4c15a2719d24fec6cde9
Publikováno v:
Open Life Sciences, Vol 18, Iss 1, Pp 572-8 (2023)
Granulomatous polyangiitis (GPA) is a rare systemic autoimmune vasculitis disease that is highly correlated with anti-neutrophil cytoplasmic antibodies (ANCAs). It was formerly called as “Wegener’s granulomatosis.” The clinical manifestations a
Externí odkaz:
https://doaj.org/article/9d838bf7026c40bab94412f353958b0c
Publikováno v:
Reumatismo, Vol 75, Iss 4 (2023)
Granulomatosis with polyangiitis (GPA) is a rare autoimmune disease that affects multiple organs and causes inflammation, necrosis, and vasculitis in small blood vessels. Treatment for GPA involves achieving and maintaining remission. In recent studi
Externí odkaz:
https://doaj.org/article/bbb192918b3e4d2c9d24064379f3431c
Publikováno v:
Case Reports in Ophthalmology, Vol 14, Iss 1, Pp 140-146 (2023)
This report presents a rare case of scleritis with peripheral ulcerative keratitis secondary to granulomatosis with polyangiitis (GPA). A 65-year-old Caucasian male presented to a regional ophthalmology service with an atypical red eye. His immune wo
Externí odkaz:
https://doaj.org/article/3209f4aee41c4f2fb49f449fbd9ce623
Publikováno v:
Indian Journal of Respiratory Care, Vol 12, Iss 2, Pp 182-184 (2023)
Granulomatosis with polyangiitis (GPA) is a necrotizing vasculitis which primarily involves upper respiratory tract, lungs and kidneys. Lung involvement is bilateral parenchymal nodules which may cavitate. We present a case of a 60-year-old male with
Externí odkaz:
https://doaj.org/article/e8162e1f811e4029922c81308aaaec93
Publikováno v:
Clinical Case Reports, Vol 11, Iss 11, Pp n/a-n/a (2023)
Key Clinical Message Here, we report a case of granulomatosis with polyangiitis presenting with unilateral parotid gland enlargement and later developed skin lesions on the lower extremities and abdomen. Although rare, salivary gland enlargement may
Externí odkaz:
https://doaj.org/article/781557d9beeb45a987a2311de4b3a8cd