Pariseau Brett, Lucarelli Mark J, Appen Richard E
Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin, USA.
Ophthalmology. 2007 Nov;114(11):2090-4. doi: 10.1016/j.ophtha.2007.05.017. Epub 2007 Aug 7.
To describe the clinical and histopathologic findings of a unique case of isolated optic nerve Blastomyces dermatitidis infection and to summarize the ophthalmic blastomycosis literature.
Case report and systematic literature review.
A 70-year-old healthy man experienced impaired vision in his left eye. Magnetic resonance imaging (MRI) showed an enhancing process of the left optic nerve sheath. Although vision initially improved with oral dexamethasone, visual acuity subsequently decreased from 20/25 to no light perception over 8 weeks. An optic nerve biopsy revealed blastomycosis. Because ophthalmic blastomycosis infections are unusual, the Cochrane Library, PubMed, OVID, and UpToDate databases were searched using the term blastomycosis with the limits English and humans. Articles that predated the databases were gathered from current references.
Visual acuity of the left eye and MRI of the orbits and brain.
Histopathologic examination of the nerve specimen showed B. dermatitidis infection. Needle biopsy and culture results of a suspicious lung scar were positive for Blastomyces. The patient was treated with intravenous amphotericin B followed by oral itraconazole for 6 months. The left eye remained blind 23 months after the biopsy. Approximately 40 articles describing ophthalmic infection were found in the literature search.
Ophthalmic blastomycosis infections can cause rapid, complete vision loss. Prompt treatment is required, but infections are uncommon and usually are misdiagnosed, often because of lack of biopsy results. Tissue must be biopsied, cultured, or both for a definitive diagnosis. Because virtually all blastomycosis cases begin in the lungs, a chest radiograph or computed tomographic scan should be obtained. Any questionable lung lesion should be biopsied to corroborate possible ophthalmic disease.
描述一例孤立性视神经皮炎芽生菌感染的临床和组织病理学表现,并总结眼部芽生菌病的文献。
病例报告和系统文献综述。
一名70岁健康男性左眼视力受损。磁共振成像(MRI)显示左侧视神经鞘有强化过程。尽管口服地塞米松后视力最初有所改善,但在8周内视力从20/25降至无光感。视神经活检显示为芽生菌病。由于眼部芽生菌病感染并不常见,因此使用“芽生菌病”一词在Cochrane图书馆、PubMed、OVID和UpToDate数据库中进行检索,并限定为英文和人类文献。早于这些数据库的文章则从当前参考文献中收集。
左眼视力以及眼眶和脑部的MRI。
神经标本的组织病理学检查显示有皮炎芽生菌感染。可疑肺部瘢痕的针吸活检和培养结果显示芽生菌呈阳性。患者接受了静脉注射两性霉素B治疗,随后口服伊曲康唑6个月。活检后23个月,左眼仍失明。在文献检索中发现约40篇描述眼部感染的文章。
眼部芽生菌病感染可导致迅速、完全失明。需要及时治疗,但感染并不常见,且通常会被误诊,这往往是因为缺乏活检结果。必须进行组织活检、培养或两者兼用以明确诊断。由于几乎所有芽生菌病病例都始于肺部,因此应进行胸部X线或计算机断层扫描。任何可疑的肺部病变都应进行活检,以证实可能的眼部疾病。