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A Case of Rhinocerebral Mucormycosis Presenting Orbital Apex Syndrome Atsushi UMEMURA 1 , Tomonao SUZUKA 1 1Department of Neurosurgery, Hamamatsu Social Insurance Hospital Keyword: rhinocerebral mucormycosis , orbital apex syndrome pp.439-442
Published Date 1998/5/10
DOI https://doi.org/10.11477/mf.1436901570
  • Abstract
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A 62-year-old man with untreated diabetes complained of diplopia and headache. Neurological examina-tion demonstrated left abducens nerve palsy. MRI showed a mass lesion in the left orbital apex. Total leftophthalmoplegia and visual loss rapidly developed in the next two weeks. A craniotomy was performed todecompress the orbital apex and remove the mass. The optic nerve was tightly encased by fibrous tissue.The pathological diagnosis was mucormycosis. Systemic administration of amphotericin B and fluconazolewas started immediately. But the lesion rapidly invaded the cavernous sinus and occluded the left internalcarotid artery. Finally, the patient died with intracranial extension of mucormycosis four months after theoperation.

Rhinocerebral mucormycosis is a rapidly progressive fatal disease. Successful treatment seems to bebased on early diagnosis, control of the underlying disease, radical surgical resection, and systemic admin-istration of amphotericin B. Mucormycosis should be considered as a differential diagnosis of orbital apexsyndrome.


Copyright © 1998, Igaku-Shoin Ltd. All rights reserved.

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