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与蝶窦毛霉菌病相关的球后视神经炎。

Retrobulbar optic neuropathy associated with sphenoid sinus mucormycosis.

作者信息

Sano Tatsuhiko, Kobayashi Zen, Takaoka Ken, Ota Kiyobumi, Onishi Iichiroh, Iizuka Mihoko, Tomimitsu Hiroyuki, Shintani Shuzo

机构信息

Department of Neurology JA Toride Medical Center Toride Ibaraki Japan.

Department of Neurology and Neurological Sciences Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Bunkyo-ku Tokyo Japan.

出版信息

Neurol Clin Neurosci. 2018 Sep;6(5):146-147. doi: 10.1111/ncn3.12216. Epub 2018 Jul 10.

Abstract

Because fungi usually spread from the paranasal sinuses to the orbital apex in invasive fungal sinusitis (IFS), IFS often presents as an orbital apex syndrome (OAS) characterized by dysfunction of cranial nerves II, III, IV, V1, and VI. We report a case of sphenoid sinus mucormycosis that presented as isolated retrobulbar optic neuropathy. A 94-year-old woman presented with acute blindness in the right eye. Examination revealed the absence of light perception and pupillary reflex in the right eye. Head MRI showed a mass in the right sphenoid sinus, which was contiguous with the right optic nerve. She underwent endoscopic surgery, and a histopathological diagnosis of mucormycosis was established. Treatment with intravenous liposomal amphotericin B reduced the size of the mass. She has survived for more than 1 year without recurrence. Clinicians should consider that IFS can present as isolated retrobulbar optic neuropathy.

摘要

由于在侵袭性真菌性鼻窦炎(IFS)中真菌通常从鼻窦扩散至眶尖,IFS常表现为眶尖综合征(OAS),其特征为Ⅱ、Ⅲ、Ⅳ、Ⅴ1和Ⅵ颅神经功能障碍。我们报告1例表现为孤立性球后视神经炎的蝶窦毛霉菌病病例。1名94岁女性因右眼急性失明就诊。检查发现右眼无光感及瞳孔反射。头部MRI显示右侧蝶窦有一肿块,与右侧视神经相邻。她接受了内镜手术,组织病理学诊断为毛霉菌病。静脉注射脂质体两性霉素B治疗后肿块缩小。她已存活1年多且无复发。临床医生应考虑到IFS可表现为孤立性球后视神经炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be04/6175081/3dec92f7499c/NCN3-6-146-g001.jpg

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