Results 141 to 150 of about 45,538 (193)

Wegener’s Granulomatosis

Otolaryngologic Clinics of North America, 1980
AbstractWegener's granulomatosis is characterized by a necrotizing granulomatous vasculitis which can be found in both the upper and lower respiratory tracts and with either focal or proliferative glomerulonephritis. However, any organ system can be affected by the disease.Over the past 17 years, 47 patients with histologically proven Wegener's ...
A D, Kornblut   +3 more
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Wegener’s Granulomatosis

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
openaire   +2 more sources

Granulomatosis with Polyangiitis (Wegener's Granulomatosis): Evolving Concepts in Treatment

Seminars in Respiratory and Critical Care Medicine, 2018
Granulomatosis with polyangiitis (GPA), formerly termed Wegener's granulomatosis, is the most common of the pulmonary vasculitides. GPA typically involves the upper respiratory tract, lower respiratory tract (bronchi and lung), and kidney, with varying ...
J. Lynch   +3 more
semanticscholar   +1 more source

WEGENER'S GRANULOMATOSIS

Annals of Internal Medicine, 1957
Excerpt Among the many clinicopathologic entities in which the fundamental lesion consists of widespread necrotizing angiitis and granuloma formation, Wegener's granulomatosis can be recognized as ...
G B, GORDON   +3 more
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Wegener's granulomatosis

The American Journal of Medicine, 1958
Abstract Wegener's granulomatosis is characterized by necrotizing granulomatous lesions of the upper respiratory tract and/or lungs, necrotizing vasculitis and focal glomerulonephritis, terminating usually in uremia. Two additional cases are reported, bringing the total in the literature to thirty-seven.
J E, TUHY, G L, MAURICE, N R, NILES
openaire   +2 more sources

Wegener's Granulomatosis

JAMA: The Journal of the American Medical Association, 1995
SELECTED CASES Patient 1 A previously healthy 20-year-old man experienced the subacute onset of an influenzalike illness characterized by diffuse arthralgias, malaise, fever, nonproductive cough, nasal congestion, epistaxis, and frontal headaches. His symptoms were unresponsive to decongestants and multiple courses of oral antibiotics.
G F, Duna, C, Galperin, G S, Hoffman
openaire   +4 more sources

WEgener's Granulomatosis

Acta Oto-Laryngologica, 1966
The authors describe the pathological picture in Wegener's granulomatosis and discLuss the etiology and pathogenesis of the disease. They report on four cases treated in Helsinki University Otolaryngological Hospital in 1964–65. The disease can be controlled to a high degree by adequate corticosteroid therapy.
B, Grahne, G, Zechner
openaire   +2 more sources

Wegener's Granulomatosis

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.
openaire   +2 more sources

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