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Intracranial germ cell tumor (iGCT)
iGCTs are intracranial homologue of gonadal germinomas (ovarian dysgerminoma, testicular seminoma)
Most common: In/near midline (80-90%)
Pineal region ~ 50-65%
Suprasellar ~ 25-35%
Less common: Basal ganglia/thalami ~ 5-10%
20% multiple
Most common = pineal with suprasellar
Pineal germinoma
Hyperdense pineal region mass engulfs pineal Ca++
Strong, often heterogeneous enhancement
T2/FLAIR hyperintensity in surrounding brain = inflammation/granulomatous change
Suprasellar germinoma
Absent posterior pituitary “bright spot”
“Fat” stalk/pituitary gland
Strong, relatively uniform enhancement
May have cysts, hemorrhage (rare)
Basal ganglia germinoma
Rare; hemorrhage common
Pineal germinoma
Pineocytoma, other pineal GCTs
Suprasellar germinoma (“fat” infundibulum)
Adult = neurosarcoid, metastases
Child = Langerhans cell histiocytosis (LCH)
90% of patients < 20 years old
Pineal region germinoma: M:F ~ 10:1
Causes dorsal midbrain syndrome
Child with diabetes insipidus? Think germinoma or LCH!
Intracranial germ cell tumor (iGCT)
Dysgerminoma, extragonadal seminoma
iGCTs are intracranial homologue of gonadal germinomas (ovarian dysgerminoma, testicular seminoma)
Best diagnostic clue
Hyperdense pineal region mass that engulfs pineal Ca++
Suprasellar mass with diabetes insipidus (DI)
BG mass with ipsilateral hemiatrophy
Location
Most common: In/near midline (80-90%)
Pineal region ~ 50-65%
Suprasellar ~ 25-35%
Less common: Basal ganglia/thalami ~ 5-10%
Other sites: Intraventricular (3rd), intrasellar, bulbar, intramedullary, midbrain, hemispheric
Size
Varies with location
Pineal: Can be large if no hydrocephalus, midbrain compression ± invasion
Infundibular stalk: Early presentation with DI common
Mass can initially be tiny/imperceptible
Number
20% multiple; most common = pineal with suprasellar
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