Results 131 to 140 of about 3,840 (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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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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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 in pregnancy
Arthritis & Rheumatism, 1997This report describes a case of severe limited Wegener's granulomatosis (WG) presenting in the third trimester of pregnancy with pansinusitis and necrotizing pneumonitis. The patient was treated successfully with a combination of corticosteroids and cyclophosphamide (CYC). The outcomes in the mother and the newborn were excellent.
P, Luisiri, N J, Lance, J J, Curran
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Wegener's granulomatosis in childhood
Pediatric Radiology, 1991The authors reviewed the medical histories and radiological examinations of five pediatric patients with a histologic diagnosis of Wegener's granulomatosis (WG) seen over a six year period in whom a total of 22 thoracic CT scans were performed. Involvement of both the upper and lower respiratory tracts was seen in all patients at presentation.
K, McHugh +4 more
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Pachymeningitis in Wegener's granulomatosis
Australasian Radiology, 1998SUMMARYA case of Wegener's granulomatosis is described in which meningeal thickening and enhancement was demonstrated on MR imaging. The diagnosis was suggested by the clinical picture, imaging findings and a positive anti‐neutrophil cytoplasmic antibody; and confirmed by biopsy of ethmoidal tissue.
H C, Burrell, N S, McConachie
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