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局限性韦格纳肉芽肿病中的双侧孤立性球后视神经炎

Bilateral isolated retrobulbar optic neuropathy in limited Wegener's granulomatosis.

作者信息

Belden C J, Hamed L M, Mancuso A A

机构信息

Department of Ophthalmology, University of Florida College of Medicine, Gainesville.

出版信息

J Clin Neuroophthalmol. 1993 Jun;13(2):119-23.

PMID:8340477
Abstract

Wegener's granulomatosis causes a variety of ophthalmologic disorders, some of which occasionally constitute the initial presentation of the disease. We describe a patient who presented with bilateral, isolated, consecutive, posterior optic neuropathy with light perception and no light perception vision. The patient had no other symptoms or signs of orbital disease. Investigations revealed cavitary lung lesions, positive antineutrophilic cytoplasmic antibody (ANCA) titers, subtle focal enhancement of the intracanalicular optic nerves on magnetic resonance imaging, and a confirmatory bronchial biopsy. This exceedingly rare ocular presentation of Wegener's granulomatosis may pose a diagnostic quandary.

摘要

韦格纳肉芽肿可导致多种眼科疾病,其中一些偶尔构成该疾病的初始表现。我们描述了一名患者,其表现为双侧、孤立、连续的后部视神经病变,有光感和无光感视力。该患者没有眼眶疾病的其他症状或体征。检查发现有空洞性肺部病变、抗中性粒细胞胞浆抗体(ANCA)滴度阳性、磁共振成像显示管内视神经有轻微局灶性强化,以及支气管活检确诊。韦格纳肉芽肿这种极其罕见的眼部表现可能会造成诊断难题。

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