A Chiari malformation is a problem in which a part of the brain at the rear of the skull bulges through a normal opening (foramen magnum) in the skull where it joins the spinal canal. This puts pressure on parts of the brain and spinal cord. It can cause mild to severe symptoms. In most cases, the problem is present at birth (congenital).
There are 4 main types of Chiari malformations (types I, II, III, and IV). Type I is the most common. This article is about type II. In this type, 2 parts of the brain (the cerebellum and brainstem) bulge through the foramen magnum.
This problem can happen in newborns who have spina bifida or spinal myelomeningoceles. A myelomeningocele is when part of the spinal cord and meninges grow outside the body instead of inside.
A common problem with type II malformations is too much spinal fluid in the brain (hydrocephalus). The extra fluid puts more pressure on the brain. The bones of the skull expand to a larger-than-normal size.
Chiari II malformations are present at birth (congenital). Medical experts don’t know what causes this malformation. They think that something happens to the fetus while it is growing that causes the brain to form abnormally. Chiari malformations may be caused when a pregnant woman is exposed to harmful substances that affect her developing baby. Or they may be a genetic problem that tends to run in families.
Signs and symptoms of Chiari II malformations depend on the age of your child. Newborns may have:
Spinal myelomeningocele or spina bifida
Noisy breathing
Trouble swallowing
Problems with breathing food or fluid into the lungs (aspiration)
Short periods of not breathing (apnea)
Weakness in the arms
Older infants and children may have:
Hydrocephalus that gets worse over time
Abnormal shape of the spine (scoliosis)
Eyesight problems
Hearing loss
Trouble using their hands to pick up and use small objects
Children may also have extra fluid in the brain stem or spinal cord (syrinx). This may cause pain in the arms or legs, or make it hard for your child to walk.
The diagnosis is often done at birth. This is because a Chiari II malformation usually occurs with other birth defects. The healthcare provider may also be able to find the defect during pregnancy with a fetal ultrasound.
The healthcare provider uses imaging tests to find Chiari malformations. Your child may need the following tests:
MRI. This test uses a combination of large magnets, radio waves, and a computer to create detailed pictures of organs and structures within the body. MRI is the best test for diagnosing Chiari malformations. If an MRI can’t be done, the provider may order a high-resolution CT scan.
CT scan. This test uses X-rays and a computer to make horizontal (axial) pictures of the body. A CT scan shows bones, muscles, fat, and organs.
Your child may need to see several kinds of healthcare providers for treatment. These include experts in brain and spinal cord problems (neurologists and neurosurgeons).
Your child’s healthcare provider will figure out the best treatment for your child based on:
How old your child is
Your child’s overall health and health history
How sick your child is
How well your child can handle certain medicines, treatments, or therapies
How long the condition is expected to last
Your opinion or preference
Treatment for a Chiari II malformation may include surgery to:
Ease pressure on the brain and let spinal fluid flow (decompression).
Close a myelomeningocele. This may be right after birth.
Put a flexible tube (shunt) in the brain. This is to drain extra fluid (hydrocephalus).
Put a shunt in the spinal cord to drain fluid from a syrinx.
Your child may also need:
Treatment for bowel and bladder problems
Special feedings
Breathing support
Complications of Chiari malformations include:
Syrinx develops or gets worse
Permanent damage to muscles or nerves
Paralysis
Too little oxygen gets to your child’s lungs (respiratory failure)
A Chiari malformation can also be fatal.
Healthcare providers can’t often tell what will happen in a child with a Chiari malformation. Your child may stay about the same. Or your child may have nerve or brain problems that get worse. Your child’s healthcare provider will watch your child closely. Your child will need physical exams and imaging tests done often.
Your child may need ongoing care:
Speech therapy for swallowing problems
Nutrition therapy
Physical, occupational, and rehabilitation therapy
Call your child’s healthcare provider if you see any changes in your child. Be sure to call if you notice problems with:
Breathing
Swallowing
Feeding
Speaking
Walking or moving
Also call your child’s provider if your child has a severe headache or neck pain.
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