Results 11 to 20 of about 98,886 (297)
Ocular manifestations in Gorlin-Goltz syndrome [PDF]
Orphanet Journal of Rare Diseases, 2019 Background Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare genetic disorder that is transmitted in an autosomal dominant manner with complete penetrance and variable expressivity. It is caused in 85% of the cases with
Antonietta Moramarco +8 more
doaj +3 more sources
Melanocitoma do nervo óptico Optic disk melanocytoma: bibliographic review [PDF]
Revista Brasileira de Oftalmologia, 2008 O melanocitoma do disco óptico é bem conhecido como uma variante do nervo melanocítico que geralmente ocorre no disco óptico. Historicamente o tumor foi confundido com melanoma maligno.
Enéias Bezerra Gouveia +1 more
doaj +3 more sources
Radiology Case Reports, 2023 Neoplasms of the orbit may be primary, secondary (infiltration from the adjacent structures), or metastatic (from distant structures). It can be divided into 3 histologic categories: benign, benign but locally aggressive, and malignant.
Ahmed T. Abdelhamid, MBChB +1 more
doaj +1 more source
Treatment of Recurrent Optic Nerve Sheath Meningioma With a Secondary Course of Radiotherapy
Cureus, 2021 Optic nerve sheath meningiomas (ONSM) are benign neoplasms found surrounding the optic nerve that can affect vision, and potentially lead to blindness.
Jibran A. Sharieff +2 more
semanticscholar +1 more source
Radiology Case Reports, 2021 The oculomotor nerve palsy is a rare neurological deficit, it is associated with numerous underlying pathologies. Including stroke, neoplasms, trauma, post-surgical inflammation, and microvascular damage from chronic disease.
Nizar Almaghrabi, MBBS +2 more
doaj +1 more source
Journal of Ophthalmology, 2021 Background: Neoplasms of the chiasmal and optic nerve region can result in compressive optic neuropathy with reduced visual acuity (VA), visual field defects and primary descending optic atrophy.
K. S. Iegorova +4 more
doaj +1 more source
Neurofibromatosis type 1-associated gliomas and other tumors: A new pathway forward?
Pediatric Hematology Oncology Journal, 2023 Neurofibromatosis type 1 (NF1) is an autosomal dominant cancer predisposition syndrome caused by germline alterations of the NF1 gene. Patients with NF1 are at increased risk for developing benign and malignant tumors, such as optic pathway glioma and ...
Andrea Webster Carrion +2 more
doaj +1 more source
Rare Retro-Orbital Intraconal Occurrence of Benign Schwannoma – A Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2013 Schwannomas otherwise referred to as neurilemmomas are benign, slowly progressing, encapsulated tumors arising from Schwann cells in the peripheral nerve sheath. They may grow along any peripheral or cranial nerve. Amongst the cranial nerve schwannomas,
A.L. Hemalatha +4 more
doaj +1 more source
Neoplasm of mixed mesenchymal and neuroepithelial origin of the optic nerve. [PDF]
British Journal of Ophthalmology, 1977 A case is reported of a 19-year-old male having right proptosis for 4 years because of a mixed meningioma and astrocytoma of the ipsilateral optic nerve. The sheath of this nerve is analogous to the leptomeninges, and neuroglial cells constitute the stroma of the nerve.
S, Shuangshoti, R, Panyathanya
openaire +2 more sources
Arquivos de Neuro-Psiquiatria, 2022 Background After a case of stroke, intracranial pressure (ICP) must be measured and monitored, and the gold standard method for that is through an invasive technique using an intraventricular or intraparenchymal device.
Ozgur Senol +4 more
doaj +1 more source