What
, as an obstetrician we should know about Sonological featurss of C P Cyst? Any
rare association with Trisomy 18?? What
is meant by CP cysts ?? Basics of C Plexus
Cysts ? Ans:- What is normal or Physiological?? The
cranial lateral ventricles contain sonolucent cerebrospinal fluid. We know
that. We also know that within the lateral ventricles lies the 3 brightly
echogenic choroid plexus that normally fills the atrium and may contain cysts .
CPCs(choroid plexus cysts) are a relatively common finding
during the second trimester especially
with current improved sonographic
technology and resolution. The reported
prevalence of echogenic CP Cysts are among normal fetuses is variable and ranges
anywhere from 0.3% to 3.65
. This variability can be accounted for
by various factors such as indications for referral completeness of the scan size criteria for
diagnosing cysts and gestational age. CPCs themselves have no known effect on fetal development
and are essentially benign.
Good news
on CPCs(choroid plexus cysts :-- In addition unlike other aneuploidy markers
there is no known association with other adverse outcomes if the
karyotype is normal.
When
sonologically CPC may be visible?? Ans:-CPCs are seen almost exclusively in fetuses between 16 to
21 weeks of gestational age and appear
to be transient . By the 23rd week of gestation they are usually undergoing regression and it is uncommon to see them sonographically
after 25 to 26 weeks cysts may be unilateral or bilateral single or multiple
and small or large . commonly they are multilocular in appearance and th cysts typically range
from between 0.5 cm and 2 cm in size Occasionally they may be so large
as to fill almost the entire lateral
ventricle and expand its walls giving
the false appearance of ventriculomegaly.
Doubt
1: Can association of CP cyst gives an signal that foetus may have Trisomy
18?? Should we insist on invasive tets to exclude aneuploidy,
if one such soft marker is visible in genetic sonogram? No, that it not done for isolated marker. Reasonig:-CPSs can be a significant finding because there have been
reports in the literature over the years describing the association of CPS with
fetal aneuploidy specifically with trisomy
18 . CPCs appear to be present in
approximately one third of trisomy 18 fetuses. Because of this association there is much debate to whether
fetuses having CPCs on ultrasound should
undergo karyotyping.
Consensus :-It
is clearly recommended that when fetuses
with CPCs have other sonographic finding invasive testing
should be offered. However when
prenatal sonography by experienced personnel reveals that the CPCs are isolated management should be conservative.
Caveat!!!!! However some investigators believe that fetuses
having isolated CPCs and no other anomalies may still carry a risk of aneuploidy
high enough to justify
amniocentesis. However the critical
component lies in whether an isolated CPC is in fact truly isolated. This can only be presumed once a detailed fetal survey by experienced examiners has
failed to reveal other structural abnormalities /markers .Therefore it is imperative
that all fetuses with CPCs
undergo a detailed fetal
sonographic anatomic survey by someone who is skilled and expe4rienced
in prenatal diagnosis.
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