1naresh
Array ( [urn:ac.highwire.org:guest:identity] => Array ( [runtime-id] => urn:ac.highwire.org:guest:identity [type] => guest [service-id] => ajnr-ac.highwire.org [access-type] => Controlled [privilege] => Array ( [urn:ac.highwire.org:guest:privilege] => Array ( [runtime-id] => urn:ac.highwire.org:guest:privilege [type] => privilege-set [privilege-set] => GUEST ) ) [credentials] => Array ( [method] => guest ) ) ) 1nareshArray ( [urn:ac.highwire.org:guest:identity] => Array ( [runtime-id] => urn:ac.highwire.org:guest:identity [type] => guest [service-id] => ajnr-ac.highwire.org [access-type] => Controlled [privilege] => Array ( [urn:ac.highwire.org:guest:privilege] => Array ( [runtime-id] => urn:ac.highwire.org:guest:privilege [type] => privilege-set [privilege-set] => GUEST ) ) [credentials] => Array ( [method] => guest ) ) )Table 3:Clinical variables associated with radiation necrosis
Statistically Significant Not Statistically Significant >3 Chemotherapy agents (P = .03) Age, 2 years or younger (P = .11) ATRT pathology (P = .03) Age, 3 years or younger (P = .34) Sex (P = 1.0) Gross total surgical resection (P = .77) Medulloblastoma tumor pathology (P = .35) Ependymoma tumor pathology (P = .15) Germinomaa (P = .3) Infratentorial tumor location (P = 1.0) Pineal tumor locationa (P = .16) Craniospinal radiation (P = .48) Total radiation dose (P = .66)
Note:—ATRT indicates atypical teratoid rhabdoid tumor.
↵a No pineal tumors or germinomas demonstrated radiation necrosis.