Neurofibromatosis type 1: optic nerve glioma and subcutaneous neurofibromas
Follow-up from clinic.
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The right optic nerve has high T2 signal and is thickened from the globe to the chiasm. The remainder of the brain is unremarkable, other than multiple stable regions of presumed chronic small vessel ischaemic change. Extensive cutaneous and subcutaneous enhancing nodules.
This patient has a known history of neurofibromatosis type 1 with optic nerve gliomas and subcutaneous neurofibromas typical manifestations.