Wegener-granulomatosis talaján kialakult krónikus gennyes középfülgyulladás komplex kezelése
نویسندگان
چکیده
منابع مشابه
Endonasal dacryocystorhinostomy in wegener granulomatosis.
Wegener granulomatosis (WG) is a life-threatening autoimmune disease of unknown etiology first described in 1936. The classic clinical triad consists of necrotizing granulomatous inflammation of the respiratory tract, necrotizing glomerulonephritis, and systemic vasculitis. Prior to the introduction of modern immunosuppressants, WG was usually fatal due to renal complications. Involvement of th...
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Wegener granulomatosis is often misdiagnosed as pneumonia and most common cause for bilateral lung infiltrates' are bacterial, viral, pneumocystis jiroveci infection. We describe a 35 year old female with 15 days history of nasal obstruction, breathlessness and fever. Investigations in this patient revealed chronic necrotizing vasculitic and granulomatous lesion in nasal biopsy, vasculitic pauc...
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Author Affiliations: Department of Ophthalmology, Emory Eye Center, Atlanta, Georgia (Drs Payne, Wells, and Grossniklaus); and Department of Ophthalmology, Cole Eye Institute, Cleveland, Ohio (Dr Srivastava). Correspondence: Dr Grossniklaus, Department of Ophthalmology, Emory Eye Center, 1365 B Clifton Rd, Room BT428, Atlanta, GA 30322 ([email protected]). Author Contributions: All of the autho...
متن کاملWegener granulomatosis masquerading as pneumonia.
We report a case of an elderly patient with a limited form of Wegener granulomatosis, which simulated the clinical and imaging features of organizing pneumonia. Here we call attention to this atypical case presentation that eloquently illustrates the many faces of Wegener granulomatosis.
متن کاملWegener granulomatosis with meningeal involvement.
The clinical, radiographic, and neuropathologic features of the case of a 41-year-old man with Wegener granulomatosis presenting with neurologic symptoms are correlated. CT and MR scans of the head demonstrated extensive meningeal thickening and enhancement. The importance of considering this diagnosis, confirmed by antineutrophil cytoplasmic autoantibodies, is emphasized.
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ژورنال
عنوان ژورنال: Orvosi Hetilap
سال: 2019
ISSN: 0030-6002,1788-6120
DOI: 10.1556/650.2018.31266