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 ) ) )Comparison of clinical, imaging, and histopathologic characteristics of PLNTYs and oligodendrogliomas
PLNTY Oligodendroglioma Age at diagnosis (yr) 16–18 40–60 Most common location Temporal lobe Frontal lobe Tumoral border Well-circumscribed Poorly defined Calcification Heavily calcified, central location of calcifications Less prominent; calcifications are classically gyriform Intralesional signal Heterogeneous Heterogeneous Enhancement Minority of tumors, typically mild Minority of tumors, typically mild (described as dotlike) Intratumoral cysts ∼90% ∼50%