Retinociliary vein associated with a craniopharyngioma.
A 60-year-old white man had a diagnosis of craniopharyngioma made in 1945. Three operations for partial tumor removal were performed in 1951, 1957, and 1962. Ophthalmoscopy and fluorescein angiography revealed bilateral optic atrophy and a large retinociliary vein in the left eye. The present report is the only example of a retinociliary vein documented with photography and fluorescein angiography. It is not possible to ascertain whether this retinociliary vein is an acquired malformation or a congenital development anomaly. The extreme rarity of this entity, though, suggests that this retinociliary vein developed as a result of obstruction, by the craniopharyngioma, to the retinal venous outflow during early development.[1]References
- Retinociliary vein associated with a craniopharyngioma. Weiter, J.J. Annals of ophthalmology. (1979) [Pubmed]
Annotations and hyperlinks in this abstract are from individual authors of WikiGenes or automatically generated by the WikiGenes Data Mining Engine. The abstract is from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.About WikiGenesOpen Access LicencePrivacy PolicyTerms of Useapsburg