Results 131 to 140 of about 2,332 (167)
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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
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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
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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
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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
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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
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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
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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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The Laryngoscope, 1983
AbstractA review of 108 patients with Wegener's granulomatosis clarified the diverse clinical manifestations and disclosed some of the less well‐known areas of involvement. Because of the frequency of nasal involvement in Wegener's granulomatosis, the otolaryngologist plays an important role in the early diagnosis and treatment.
T J, McDonald, R A, DeRemee
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AbstractA review of 108 patients with Wegener's granulomatosis clarified the diverse clinical manifestations and disclosed some of the less well‐known areas of involvement. Because of the frequency of nasal involvement in Wegener's granulomatosis, the otolaryngologist plays an important role in the early diagnosis and treatment.
T J, McDonald, R A, DeRemee
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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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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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Wegener's granulomatosis of the breast
Wiener klinische Wochenschrift, 2006Wegener's granulomatosis is a multisystem disorder characterized by necrotizing granulomatous inflammation and vasculitis of small vessels and can affect any organ system. The most common sites of involvement are upper and lower respiratory tracts, and kidneys. Breast involvement is unusual and very rare.
Neralić-Meniga, Inja +6 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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