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CHAPTER 34 The Fetal Brain 1209

V

A

B

C

FIG. 34.37 Intracranial Teratoma. (A) Sonogram at 34 weeks

shows teratoma forming an echogenic mass with small cystic spaces

(arrows) displacing the midline to one side. The visible lateral ventricle

(V) is dilated. (B) In a different fetus, a facial teratoma invades the

brain. (C) Magnetic resonance image of same fetus in (B) shows

the intracranial extent of the tumor.

indings include polyhydramnios and intracranial hemorrhage.

Diagnosis is typically made in the third trimester on ultrasound

triggered by excessive uterine growth due to polyhydramnios,

although teratomas have been discovered as early as 17 weeks.

Fetuses suspected to have brain tumors should undergo detailed

ultrasound examination to look for associated abnormalities,

which can occur in about 12% of cases, especially involving the

face. Most have normal karyotype. MRI is helpful in characterizing

the mass, evaluating tumor extension, and diferentiating tumors

from other conditions such as hemorrhage, sinus thrombosis,

and vascular malformations. 251,252

Outcomes are poor, especially if tumors appear early. Overall

survival is about 28% and relates to size and location of tumor,

its histology, surgical resectability, response to chemotherapy,

and condition of the fetus at diagnosis. he large head size can

interfere with delivery and require cephalocentesis to allow vaginal

delivery. Of the few survivors, almost all have long-term neurologic

deicits. Slightly better survival is seen with choroid plexus

papilloma (73%) and meningeal tumors (36%). 251-253

Choroid plexus papillomas are large, inely nodular masses

that grow into the lateral ventricle and produce excessive CSF,

resulting in severe dilation of the entire ventricular system and

macrocephaly. Most are sporadic, but a few are associated with

Aicardi syndrome and giant pigmented nevi. Surgical resection

can be curative but is technically diicult because the vascular

nature of choroid plexus papillomas can result in fatal hemorrhage.

Overall survival is about 73%. 251

Intracranial lipomas are not “neoplasms” but rather a

malformation of meninx primitiva development. Instead of

resorbing at 8 to 10 weeks, the meninx persists and develops

into a mass of mature adipose tissue. he incidence is 4 to 40

per 100,000 autopsies. Most are near the corpus callosum, but

they can arise in any cistern. hey can interfere with callosal

development, and associated dysgenesis of the corpus callosum

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