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Retrobulbar optic neuropathy associated with sphenoid sinus mucormycosis.
Sano, Tatsuhiko; Kobayashi, Zen; Takaoka, Ken; Ota, Kiyobumi; Onishi, Iichiroh; Iizuka, Mihoko; Tomimitsu, Hiroyuki; Shintani, Shuzo.
Afiliação
  • Sano T; Department of Neurology JA Toride Medical Center Toride Ibaraki Japan.
  • Kobayashi Z; Department of Neurology and Neurological Sciences Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Bunkyo-ku Tokyo Japan.
  • Takaoka K; Department of Neurology JA Toride Medical Center Toride Ibaraki Japan.
  • Ota K; Department of Neurology JA Toride Medical Center Toride Ibaraki Japan.
  • Onishi I; Department of Neurology and Neurological Sciences Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Bunkyo-ku Tokyo Japan.
  • Iizuka M; Department of Neurology JA Toride Medical Center Toride Ibaraki Japan.
  • Tomimitsu H; Department of Comprehensive Pathology Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Bunkyo-ku Tokyo Japan.
  • Shintani S; Department of Ophthalmology JA Toride Medical Center Toride Ibaraki Japan.
Neurol Clin Neurosci ; 6(5): 146-147, 2018 Sep.
Article em En | MEDLINE | ID: mdl-30333924
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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article