Retinoblastoma CT: Difference between revisions
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{{Retinoblastoma}} | {{Retinoblastoma}} | ||
==CT scan== | ==CT scan== | ||
On CT, retinoblastoma is characterized by enhancing intermediate-density soft-tissue mass or masses, with varying degrees of calcification.<ref name="pmid10915702">{{cite journal |author=Kaste SC, Jenkins JJ, Pratt CB, Langston JW, Haik BG |title=Retinoblastoma: sonographic findings with pathologic correlation in pediatric patients |journal=[[AJR. American Journal of Roentgenology]] |volume=175 |issue=2 |pages=495–501 |year=2000 |month=August |pmid=10915702 |doi= |url=http://www.ajronline.org/cgi/pmidlookup?view=long&pmid=10915702 |accessdate=2012-05-29}}</ref> CT detects intraocular, extraocular, and intracranial disease extension, is very good at delineation of bony abnormalities and readily depicts tumoral calcifications with a sensitivity greater than 90%. | |||
However, delineation of intraocular soft tissue detail is limited and the sensitivity of CT to detect optic nerve invasion is very low even in patients with extensive optic nerve invasion. | |||
==References== | ==References== |
Revision as of 19:56, 29 May 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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CT scan
On CT, retinoblastoma is characterized by enhancing intermediate-density soft-tissue mass or masses, with varying degrees of calcification.[1] CT detects intraocular, extraocular, and intracranial disease extension, is very good at delineation of bony abnormalities and readily depicts tumoral calcifications with a sensitivity greater than 90%. However, delineation of intraocular soft tissue detail is limited and the sensitivity of CT to detect optic nerve invasion is very low even in patients with extensive optic nerve invasion.
References
- ↑ Kaste SC, Jenkins JJ, Pratt CB, Langston JW, Haik BG (2000). "Retinoblastoma: sonographic findings with pathologic correlation in pediatric patients". AJR. American Journal of Roentgenology. 175 (2): 495–501. PMID 10915702. Retrieved 2012-05-29. Unknown parameter
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