Medulloepithelioma (Q95221): Difference between revisions
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Meduloepiteliomas são um tipo raro de tumor neuroectodérmico primitivo dos primeiros anos de vida ou da infância, originado do epitélio medular primitivo no olho e localizado mais frequentemente na medula espinhal e no cérebro. Ocasionalmente compromete o nervo óptico manifestando-se com perda de visão, estrabismo, proptose e dor. | |||
| description / en | description / en | ||
Medulloepitheliomas are a rare type of primitive neuroectodermal tumour of infancy or childhood, originating from the primitive medullary epithelium in the eye and located most often in the spinal cord and brain but occasionally in the optic nerve and manifesting with vision loss, strabismus, proptosis and pain. | |||
Revision as of 10:56, 16 August 2026
Medulloepitheliomas are a rare type of primitive neuroectodermal tumour of infancy or childhood, originating from the primitive medullary epithelium in the eye and located most often in the spinal cord and brain but occasionally in the optic nerve and manifesting with vision loss, strabismus, proptosis and pain.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1078680756 |
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| English | Medulloepithelioma |
Medulloepitheliomas are a rare type of primitive neuroectodermal tumour of infancy or childhood, originating from the primitive medullary epithelium in the eye and located most often in the spinal cord and brain but occasionally in the optic nerve and manifesting with vision loss, strabismus, proptosis and pain. |
