eye neoplasms/seizures

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Pigmented adenoma mimicking a juxtapapillary melanoma. A 20-year follow-up.

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A 52-year-old white woman was first diagnosed with a tumor of the right optic nerve in 1972. She remained asymptomatic until 1992, when she had a seizure on the left side of her body from a frontoparietal glioblastoma multiforme. Ophthalmic examination revealed enlargement of the eye tumor. This

Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis.

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Encephalocraniocutaneous lipomatosis (ECCL) is a sporadic condition characterized by ocular, cutaneous, and central nervous system anomalies. Key clinical features include a well-demarcated hairless fatty nevus on the scalp, benign ocular tumors, and central nervous system lipomas. Seizures,

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