Indolent orbital apex syndrome caused by occult mucormycosis.

D P Dooley, D A Hollsten, S R Grimes, J Moss
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Abstract

The chronic or indolent presentation of rhino-orbital mucormycosis, as defined by the presence of symptoms for more than 1 month before diagnosis, is extremely unusual. A 45-year-old man with stable diabetes presented with a right orbital apex syndrome and minimal ethmoid and sphenoid sinusitis. Progression was indolent, and the diagnosis was not made until 7 weeks after admission, when a third biopsy was prompted by new cavernous sinus and carotid artery thromboses. Mucormycosis was found. The patient improved on amphotericin B (2 g) and strict blood glucose control. A remarkable aberrant regeneration of the right oculomotor nerve was seen following treatment. He remains free of active disease 4 years later. Orbital symptoms in well-controlled diabetics, which may even remain stable for weeks and lack direct signs of tissue invasion, should raise the suspicion of mucormycosis.

隐匿性毛霉病引起的眶尖惰性综合征。
鼻眶毛霉菌病的慢性或惰性表现,在诊断前症状超过1个月,是非常罕见的。45岁男性糖尿病患者表现为右眼眶尖综合征和轻度筛蝶窦炎。进展缓慢,直到入院后7周才确诊,当时第三次活检提示新的海绵窦和颈动脉血栓形成。发现毛霉病。患者经两性霉素B (2 g)治疗及严格血糖控制后病情好转。治疗后发现右动眼神经再生异常。4年后,他仍然没有活动性疾病。在控制良好的糖尿病患者中,眼眶症状甚至可以保持数周的稳定,没有直接的组织侵犯迹象,这应该引起对毛霉病的怀疑。
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