Figure 4: coronal view of fetal unilateral cerebral borderline ventriculomegaly
Table 1: a summary of the outcomes of infants with a prenatal diagnosis of borderline cerebral ventriculomegaly.
|
Aneuploidies
|
9/234
|
3.8%
|
Malformations undiagnosed in utero
|
19/221
|
8.6%
|
Perinatal deaths
|
8/209
|
3.7%
|
Abnormal development
|
24/209
|
11.5%
|
Abnormal outcome (overall)
|
43/219
|
19.6%
|
Obstetrical management: A search for associated congenital anomalies including echocardiography is indicated. Limited data exist with regard to the association with chromosomal aberrations. However, the available studies report aneuploidies in 4% of cases, mostly trisomy 21. We believe therefore that at present it would be prudent to offer a procedure for fetal karyotyping. A workup for a congenital infection associated with hydrocephalus (i.e., toxoplasmosis, cytomegalovirus, and rubella) is also commonly recommended, although thus far an association has not been demonstrated. Infants with isolated borderline cerebral ventriculomegaly are at increased risk for developmental delay. It has been suggested that this finding could represent an indication for early childhood intervention, as special educational programs maximize the developmental potential.[13] However, counseling these couples is a major undertaking. It has been our experience that the communication that the infant has even a slightly increased risk of cerebral damage or low intellect causes major distress to most couples. We expect that at least some patients will request termination of pregnancy. This will raise a difficult ethical dilemma, as most cases of isolated borderline cerebral ventriculomegaly result in the birth of healthy infants. In continuing pregnancies, borderline cerebral ventriculomegaly is not an indication to modify standard obstetric care. We believe that serial scans should be performed, as in a handful of cases, ventriculomegaly and macrocrania may develop.
Reference
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