- Contain all three germ cell
layers.
- Usually benign, but grow
rapidly, invade locally and do not metastasize.
- 2/3 supratentorially and
thought to arise from the pineal gland.
- Usually diagnosed in the
third trimester (earliest reported teratoma was at 22 weeks).
- Irregular.
- Solid echogenic mass with
variable cystic components.


- Calcification (may be
sonographically visualized).
- Distortion of the fetal
brain; midline structures may not be identified.
- Majority are supratentorial.
3 sites of predilection
- Within the third
ventricle (having invaded from the pineal gland).
- Subfrontal.
- Subtemporal.
- Less frequently they may
arise infratentorially.
- Can grow through the
skull base into the neck, midbrain and orbits
- Increased BPD and hydrocephalus
may occur, resulting in macrocrania with / without deformity of the
calvarial shape.
- Polyhydramnios (>50%).
- Fetal hydrops and high output
cardiac failure is rare (1).
|
Scan at 22 weeks of gestation.Solid subfrontal mass
extending into temporal and parietal regions.Solid and predominatly cytic
components.Mass effect and midline shift present. Dilated third ventricle
|
|

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|
·
TORCH infection.
·
Ischemic brain necrosis.
·
Other intracranial tumors (astrocytoma /
neuroectodermal).
·
Arachnoid cyst if the lesion is primarily cystic.
- Very poor. Perinatal
mortality is close to 100% (usually in the first few days of life).
- Prolonged survival is rare,
but has been described.
- Scherer DM, Abramowicz JS
Eggers PC et.al. Prenatal ultrasonic diagnosis of intracranial teratoma
and massive craniomegaly with associated high-output cardiac failure. Am J
Obstet Gynecol 1993;168:97-99.
- Richard SR. Ultrasonic
diagnosis of intracranial teratoma in utero: A case report and literature
review. J Reprod Med 1987;32:73-75.
- Ferreira O, Morvan J,
Cleophax JP. Prenatal diagnosis of intracranial teratoma. A case report. J
Gynecol Obstet Biol Reprod 1988;17:1075-1080.
- Ferreira J, Eviatar L,
Schneider S et.al. Prenatal diagnosis of intracranial teratoma: Prolonged
survival after resection of a malignant teratoma diagnosed prenatally by
ultrasound. A case report and literature review. Pediatr Neurosurg
1993;19:84-88.
- Kuller JA, Laifer SA, Martin
JG et.al. Unusual presentation of fetal teratoma. J Perinatol
1991;11:294-296.