Results 131 to 140 of about 3,790 (148)
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Survey of Ophthalmology, 1998
Clinical manifestations of Wegener's granulomatosis are nonspecific and indistinguishable from a variety of neoplastic, infectious, and inflammatory diseases. Ophthalmic disease is the presenting feature in nearly one sixth of patients with Wegener's granulomatosis and will ultimately develop in a majority.
L E, Harman, C E, Margo
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Clinical manifestations of Wegener's granulomatosis are nonspecific and indistinguishable from a variety of neoplastic, infectious, and inflammatory diseases. Ophthalmic disease is the presenting feature in nearly one sixth of patients with Wegener's granulomatosis and will ultimately develop in a majority.
L E, Harman, C E, Margo
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Archives of Dermatology, 1960
Wegener's granulomatosis is a fatal systemic disease; its course may be acute or chronic. Pathologically it is identified by three constant abnormal findings; this triad is pathognomonic of the syndrome: Necrotizing granulomatous ulceration of the upper portion of the respiratory tract. Granulomatous inflammation of the lungs.
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Wegener's granulomatosis is a fatal systemic disease; its course may be acute or chronic. Pathologically it is identified by three constant abnormal findings; this triad is pathognomonic of the syndrome: Necrotizing granulomatous ulceration of the upper portion of the respiratory tract. Granulomatous inflammation of the lungs.
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Localized Wegener’s granulomatosis
Journal of the European Academy of Dermatology and Venereology, 2011AbstractBackground Wegener’s granulomatosis (WG) is a rare granulomatous necrotizing vasculitis of small and medium vessels which has predilection for upper airways, lungs and kidney. However, any other organ, including the skin and oral cavity, can be involved.
A.V. Marzano +5 more
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The American Journal of the Medical Sciences, 2001
Wegener granulomatosis (WG) is a necrotizing, granulomatous vasculitis that has a clinical predilection to involve the upper airways, lungs, and kidneys. Although the first case was reported by Klinger in 1931, Friedrich Wegener in 1936 characterized the unique clinical and pathological features of this disease that subsequently came to bear his name ...
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Wegener granulomatosis (WG) is a necrotizing, granulomatous vasculitis that has a clinical predilection to involve the upper airways, lungs, and kidneys. Although the first case was reported by Klinger in 1931, Friedrich Wegener in 1936 characterized the unique clinical and pathological features of this disease that subsequently came to bear his name ...
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Intracranial Wegener's granulomatosis
Neurology, 1993We describe an atypical neurologic presentation of Wegener's granulomatosis (WG) with striking meningeal and cerebral involvement, responding to immunosuppressive therapy. WG may cause treatable intracranial complications in the absence of nasal or renal disease and without cerebral angiographic abnormalities, CSF pleocytosis, or a positive assay for ...
L M, Weinberger +4 more
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Intracardiac Wegener's Granulomatosis
The Annals of Thoracic Surgery, 2012A healthy 22-year-old woman presented with acute ventricular tachycardia. Cardiac magnetic resonance imaging revealed a mass in the left ventricular cavity. On the basis of these findings, a provisional diagnosis of rhabdomyosarcoma was made and the patient was scheduled to undergo an immediate cardiac surgical procedure.
Omair, Shakil +4 more
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Limited Wegener's Granulomatosis
Australasian Radiology, 1984ABSTRACT6 cases of limited Wegener's Granulomatosis are presented.There were 4 males and 2 females, with a mean age of 48 years.Predominant organ systems involved were the upper and lower respiratory tracts, eyes and ears, with isolated involvement of the joints, gall bladder and adrenals.Chest Radiographic features included large rounded masses ...
C, Perry, J E, Shevland
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Renal Limited Wegener’s granulomatosis
Lupus, 2009Differential diagnosis in patients presenting with fever of unknown origin (FUO) is often difficult because infectious diseases, neoplasms, infective endocarditis or systemic autoimmune diseases may all be responsible for the condition. Furthermore, vasculitis may generate typical, atypical or limited syndromes depending on the extent of vascular ...
DEL PORTO, Flavia +5 more
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Current Opinion in Rheumatology, 1991
Wegner's granulomatosis is a clinicopathologic syndrome of unknown etiology characterized by granulomatous vasculitis of the upper and lower respiratory tracts and glomerulonephritis. During the period covered by this review several articles were published describing the clinical and pathologic features of Wegner's granulomatosis.
R Y, Leavitt, A S, Fauci
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Wegner's granulomatosis is a clinicopathologic syndrome of unknown etiology characterized by granulomatous vasculitis of the upper and lower respiratory tracts and glomerulonephritis. During the period covered by this review several articles were published describing the clinical and pathologic features of Wegner's granulomatosis.
R Y, Leavitt, A S, Fauci
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