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Solitary neurofibroma of the orbit with intracerebral extension associated with ocular surface melanocytoma: a case report
Published in Orbit, 2020
Mansooreh Jamshidian-Tehrani, Raziyeh Mahmoudzadeh, Esmaeil Asadi Khameneh, Fahimeh Asadi Amoli, Morteza Faghih Jouibari, Abolfazl Kasaee, Hadi Ghadimi
The patient had dysplasia of greater wing of sphenoid bone and one neurofibroma, which was classified as diffuse neurofibroma. His neurofibroma was not plexiform and he did not have any other diagnostic criteria for NF-1.8 Therefore he did not have Von Recklinghausen’s disease according to NIH consensus guidelines8 and his neurofibroma is classified as solitary. In the absence of other features of neurofibromatosis, the diagnosis of these solitary tumors is more difficult and they may be mistaken for schwannomas and other orbital tumors.9,10