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韦格纳肉芽肿的眼部表现。十五年经验及文献综述。

The ocular manifestations of Wegener's granulomatosis. Fifteen years experience and review of the literature.

作者信息

Haynes B F, Fishman M L, Fauci A S, Wolff S M

出版信息

Am J Med. 1977 Jul;63(1):131-41. doi: 10.1016/0002-9343(77)90125-5.

Abstract

Ocular manifestations of Wegener's granulomatosis may occur secondary to contiguous granulomatous sinusitis or as a result of focal vasculitis. Contiguous granulomatous sinus disease causes nasolacrimal duct obstruction, proptosis and ocular muscle or optic nerve involvement. Focal vasculitis unrelated to contiguous upper respiratory tract disease is manifested by conjunctivitis, episcleritis, scleritis, corneoscleral ulceration, uveitis, and granulomatous vasculitis of the retina and optic nerve. A review of 29 cases of Wegener's granulomatosis and three cases of lymphomatoid granulomatosis studied over the past 15 years at the National Institute of Allergy and Infectious Diseases (NIAID) disclosed single or multiple ocular manifestations of disease in 15 patients (47 per cent). The pattern of ocular disease, its relationship to systemic involvement, diagnostic methods and the response to therapy are discussed.

摘要

韦格纳肉芽肿病的眼部表现可能继发于相邻的肉芽肿性鼻窦炎,或由局灶性血管炎引起。相邻的肉芽肿性鼻窦疾病可导致鼻泪管阻塞、眼球突出以及眼肌或视神经受累。与相邻上呼吸道疾病无关的局灶性血管炎表现为结膜炎、巩膜外层炎、巩膜炎、角膜巩膜溃疡、葡萄膜炎以及视网膜和视神经的肉芽肿性血管炎。美国国立过敏和传染病研究所(NIAID)在过去15年里对29例韦格纳肉芽肿病和3例淋巴瘤样肉芽肿病进行了研究,发现15例患者(47%)出现了单眼或多眼疾病表现。本文讨论了眼部疾病的模式、其与全身受累的关系、诊断方法以及对治疗的反应。

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