Results 11 to 20 of about 50,602 (199)
Wegener’s granulomatosis [PDF]
Wegener’s granulomatosis is a necrotizing inflammation of small and medium size vessels with granuloma formation. It is a very heterogeneous disease in respect of severity and clinical manifestation. While it can be a rapidly progressive disease with fatal ending, there are forms limited only to one organ.
Gadó, Klára +3 more
openaire +5 more sources
Cytomegalovirus retinitis presenting as vasculitis in a patient with Wegener’s granulomatosis
Paris G Tranos1, Ilias Georgalas2, Panagiota Founti1, Ioannis Ladas21Papageorgiou University Hospital, Thessaloniki, Greece; 2Department of Ophthalmology, “G.Genimatas” Hospital, Athens, GreecePurpose: To present an unusual case of ...
Paris G Tranos +3 more
doaj +1 more source
Cytomegalovirus retinitis treated with valganciclovir in Wegener’s granulomatosis
Yoshiaki Kabata1, Genichiro Takahashi1, Hiroshi Tsuneoka21Department of Ophthalmology, Jikei University School of Medicine, Katsushika Medical Center, Katsushika, Tokyo, Japan; 2Department of Ophthalmology, Jikei University School of Medicine, Minato ...
Kabata Y, Takahashi G, Tsuneoka H
doaj +1 more source
Granulomatose de Wegener Wegener's granulomatosis
A granulomatose de Wegener caracteriza-se por vasculite necrosante granulomatosa que acomete preferencialmente vias aéreas superiores, inferiores e rins.
Telma Antunes +1 more
doaj +2 more sources
Orbital granulomatosis with polyangiitis (Wegener granulomatosis): clinical and pathologic findings. [PDF]
The pathology of granulomatosis with polyangiitis (GPA), formerly Wegener granulomatosis, typically features a granulomatous and sometimes necrotizing vasculitis targeting the respiratory tract and kidneys. However, orbital involvement occurs in up to 60%
Muller K, Lin JH.
europepmc +2 more sources
Wegener Granulomatosis with Oral Involvement as Primary Manifestation: A Case Study [PDF]
Introduction: Wegener Granulomatosis is a rare multisystemic disease with an unknown cause, characterized by necrotic granulomatous lesions in respiratory tract, systemic vasculitis in small arteries and veins and necrotizing glomerulonephritis.
Mahdokht Rashed +5 more
doaj +1 more source
Granulomatosis with polyangiitis: A case report and brief review of literature
: Granulomatosis with polyangiitis formerly known as Wegener's granulomatosis was first described by German pathologist Friedrich Wegener in 1936. It is a multi-system necrotizing noncaseating granulomatous vasculitis which affects small to medium-sized ...
Dhairya A Lakhani, MD +6 more
doaj +1 more source
Wegener's Granulomatosis [PDF]
WG is an uncommon disease process with considerable risk of mortality if diagnosis and treatment are delayed. Skin, sinus, or oral mucosal lesions may be part of the initial presentation. This article provided the clinician with information concerning recognition, diagnosis, and treatment of WG. Early recognition and treatment are essential in limiting
Lawrence W, Weeda, Stephen A, Coffey
openaire +4 more sources
Wegener's granulomatosis is an organ- and/or life-threatening autoimmune disease of as yet unknown etiology. The classic clinical triad consists of necrotizing granulomatous inflammation of the upper and/or lower respiratory tract, necrotizing glomerulonephritis, and an autoimmune necrotizing systemic vasculitis affecting predominantly small vessels ...
Marjan C, Slot +1 more
openaire +4 more sources
Manifestaciones periodontales de la Granulomatosis de Wegener: Reporte de un caso clínico
La granulomatosis de Wegener o granulomatosis con Poliangitis (GPA) es una enfermedad caracterizada por inflamación y necrosis de las paredes de los vasos sanguíneos. Es de etiología desconocida, baja prevalencia y alta agresividad. Esta enfermedad puede
Natalia Tornel +3 more
doaj +1 more source

