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Primary parenchymal neoplasm of pineal gland
Intermediate in malignancy between pineoblastoma and pineocytoma
General features
Aggressive-looking pineal mass in adult
Extension into adjacent structures (ventricles, thalami) is common
Lobulated, moderately vascular
Size varies from small (< 1 cm) to large (~ 6 cm)
CT
Hyperdense mass centered in pineal region
Engulfs pineal gland Ca++
Hydrocephalus
MR
T1: Mixed iso-/hypointense mass
T2: Isointense with gray matter, + small hyperintense foci
FLAIR: Hyperintense
Strong, heterogeneous enhancement
MRS: Elevated Cho, decreased NAA
If aggressive-looking pineal region tumor in middle-aged, older adult, consider PPTID
Germinoma
Pineocytoma
Pineoblastoma
Papillary tumor of pineal region
Neuroepithelial neoplasm
Arises from pineocytes or their precursors
WHO grade II or III
Dorsal midbrain (Parinaud) syndrome, headache
Upgaze paralysis, convergence-retraction nystagmus
Pineal parenchymal tumors (PPT)
Pineal parenchymal tumor of intermediate differentiation (PPTID)
“Atypical pineocytoma” (old)
Primary parenchymal neoplasm of pineal gland
Intermediate in malignancy between pineocytoma and pineoblastoma
Pineocytoma: Slow-growing neoplasm with small mature cells that resemble pineocytes
Adults predominate
Well-differentiated histology with large “pineocytomatous rosettes”
Indolent course (imaging may remain stable for years)
Generally good prognosis
Pineoblastoma: Highly malignant primitive embryonal tumor of pineal gland
Occurs primarily (but not exclusively) in children
Poorly differentiated
Aggressive behavior
Poor prognosis
Best diagnostic clue
Aggressive-looking pineal mass in adult
Location
Pineal gland mass
Extension into adjacent structures common: Ventricles, tectum, thalamus
CSF dissemination (rare)
Size
Varies from small (< 1 cm) to ~ 6 cm
Morphology
Lobulated, moderately vascular
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