Hydrocephalus is a brain condition
that gets its name from the Greek word for water (meaning "hydro")
and head (meaning "cephalus"). It occurs when cerebral spinal fluid
(CSF) — the clear, water-like fluid that surrounds and cushions the brain and
spinal cord — is unable to drain from the brain. It then pools, causing a
backup of fluid in the skull.
Sometimes
referred to as "water on the brain," hydrocephalus can cause babies'
and young children's heads to swell to accommodate the excess fluid. Older
kids, whose skull bones have matured and fused together, experience painful
headaches due to increased pressure in the head.
If left untreated, hydrocephalus can
lead to brain damage, a loss in mental and physical abilities, and even death.
With early diagnosis and timely treatment, however, most children recover
successfully.
Causes
of Hydrocephalus
When everything is working normally
inside the brain, CSF will flow through narrow passageways called ventricles
and exit the brain through a small reservoir at the base of the brain called
the cistern. CSF is responsible for delivering nutrients to the brain and
taking waste away from sensitive areas, where it will eventually be absorbed
into the bloodstream.
If a blockage
exists in any of the ventricles, CSF backs up and causes an excess of fluid in
the brain, or hydrocephalus. This accumulation of fluid can also happen when
the choroid plexus (the area of the brain that produces CSF) is in overdrive or
if the fluid fails to be properly absorbed by the bloodstream.
When
hydrocephalus is present at birth, it can be the result of conditions like spina
bifida (where the
primary cause is abnormal development of the spinal cord) or aqueductal
stenosis (a narrowing of the small passageway, called the "aqueduct of
Sylvius," that connects two major ventricles in the brain).
Acquired
hydrocephalus is caused by cranial hemorrhage, or bleeding in the brain. This
can happen in premature babies or kids who've undergone traumatic head
injuries.
But not every case of hydrocephalus is
due to the causes mentioned here: Some kids can develop hydrocephalus without a
known cause.
Signs
in Babies
Symptoms of
hydrocephalus vary depending on the age of a child.
Infants and babies under the age of 1
year will appear to have significant swelling of the head. Their skull bones —
thin, bony plates that have not yet fused together — are connected by fibrous
tissue called sutures. These sutures, or "soft spots," have not yet
hardened and therefore stretch and protrude to accommodate the excess CSF.
As a result, a
baby with hydrocephalus will appear to have an abnormally shaped head — usually
much larger than other babies the same age. Other signs to look for include:
- bulging at the soft spots
- "split" sutures — a gap
can be felt between skull bones
- rapid increase in head
circumference
- swollen veins that are
recognizable to the naked eye
- downward cast of the eyes (called
"sunsetting")
Depending on the
severity of the condition, kids may also experience sleepiness, irritability,
vomiting, and seizures. In extreme cases, a child may also experience "failure to thrive," meaning that he or she might miss
growth or developmental milestones or may revert to earlier developmental
stages.
Signs in Older
Kids
Older children
will not have the easily recognizable symptom of an enlarged head because their
skull bones have fused together and therefore cannot expand to accommodate the
excess fluid.
In these cases, pressure on the brain
intensifies and causes severe headaches that may wake a child in the middle of
the night or early in the morning. Headaches may be coupled with:
- nausea/vomiting
- sleepiness
- difficulties with balance and
motor skills
- double vision
- squinting and/or other repetitive
eye movements
- seizures
Changes in
personality, loss of new developmental abilities (like speaking or walking),
and memory loss may also occur in more advanced cases.
Diagnosis
A child who shows any of the signs and
symptoms mentioned above should be evaluated by a doctor right away. The doctor
will perform examinations, which may include a medical history and diagnostic
imaging — like ultrasound, CT (computed tomography), or MRI (magnetic resonance
imaging) — to get a clear picture of the inside of the brain.
During
imaging, a child will lie still on a table for a few seconds while a machine
passes over his or her body, emitting very low (and harmless) frequencies of
radiation or sound waves.
Shunt
Procedure
If hydrocephalus is diagnosed, treatment will
depend on the age of the child, the cause of the cerebral spinal fluid build-up
(whether from a blockage, overproduction of fluid, or another problem), and the
child's overall health.
Shunt procedures, which have been the standard
of care for decades, involve surgically implanting one end of a catheter
(flexible tube) into a ventricle of the brain and placing the other end in the
abdominal cavity, chambers of the heart, or space around the lungs where fluid
is drained and absorbed by the bloodstream. A valve in the shunt system
regulates flow to prevent over-draining and under-draining.
While shunting is often an effective treatment
for hydrocephalus, there is a high chance of failure and complications. About
30% of shunts will stop working within the first year, with about 5% failing in
each subsequent year, causing symptoms to recur. A child will need to have
surgery to correct the problem — whether it requires replacing a catheter or
valve or replacing the entire shunt. Most kids who undergo shunting will
require subsequent operations over their lifetimes to regulate shunt problems.
Infections are another side effect of
shunting, and occur in 5%-10% of shunt operations. Kids will develop typical
signs of infection, like fever and neck stiffness, and may feel tenderness
along the shunt or belly pain. Most infections develop within the first several
months after a shunt procedure and require temporary removal of the device
while a child receives intravenous antibiotics for up to 2 weeks.
Ventriculostomy
A second, increasingly more common treatment
for hydrocephalus is an endoscopic third ventriculostomy. During this
procedure, a small opening is made in the bottom of the third ventricle (one of
four ventricles in the brain) to allow fluid to exit the brain.
This minimally invasive approach involves
placing an endoscope (small lighted camera) inside the brain to provide
surgeons with a view of the surgical site on a computer monitor. Then, using
very small instruments, the doctor will make a tiny hole in the bottom of the
third ventricle, where a thin membrane separates the inside and outside of the
brain. This new "evacuation route" permits fluid to drain normally
into the spaces outside the brain while bypassing any obstructions that are
causing a backup, so the body can reabsorb the CSF back into the bloodstream as
it normally would.
When deemed appropriate, third
ventriculostomies are the procedure of choice for kids older than 6 months of
age due to a higher efficacy rate and lower risk of infection than shunting.
Those who undergo the procedure have up to a 90% chance of long-term success,
with little need for follow-up procedures.
Third ventriculostomies also have shown
promise in newborns and may be offered as a treatment to these younger patients
in the near future.
Outlook
With
timely treatment, many kids with hydrocephalus go on to lead normal lives.
Those
with more complex medical problems, like spina bifida or bleeding in the brain
from prematurity, may experience a higher rate of complications due to their
underlying medical conditions. In these kids, early intervention greatly
improves the chances of recovery.
Tidak ada komentar:
Posting Komentar