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Article
May 1988

Neurilemoma as a Presenting Feature of Neurofibromatosis

Author Affiliations

From the Department of Ophthalmology, Washington University School of Medicine, St Louis.

Arch Ophthalmol. 1988;106(5):665-667. doi:10.1001/archopht.1988.01060130719032
Abstract

• A previously healthy 38-year-old woman presented with gradually progressive ptosis and downward deviation of her left eye and a palpable left superonasal orbital mass. The mass was excised, and histopathologic examination revealed a tumor composed of spindle cells arranged in both Antoni A and B patterns. Presence of S-100 antigen was determined by immunoperoxidase staining. The diagnosis was neurilemoma. A right apical extraparenchymal mass detected on a preoperative chest roentgenogram and computed tomography was most consistent with a benign neurogenic tumor. The presentation was that of a recently discovered neurilemoma in a patient with preexisting, but previously undiagnosed, neurofibromatosis.

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