Chiari malformation is a congenital structural, (meaning its present at birth) problem at the base of the skull that affects the brain and spinal cord. In fact it is not a malformation of the brain at all. More accurately, the lower portion of the skull, the portion known as the posterior fossa, is too small to accommodate the lower portion of the brain. As a result, a portion of the cerebellum called the tonsils is forced to protrude into the spinal column. This results in compression of the brain stem and spinal cord and interferes with the flow of spinal fluid. It is the compression of the brain stem and spinal cord that is primarily responsible for the symptoms. We have learned that compression that is sufficient to cause symptoms can occur even when the cerebellar tonsils protrude by as little as 1 millimeter.
Despite the fact that Chiari malformation is usually present at birth, the symptoms of the malformation are usually not experienced until adulthood, usually when the patient is in their 20s or 30s. Symptoms can develop sooner or later than this. Chiari malformation is often difficult to diagnose because the symptoms can be vague and so numerous that many doctors just can’t make sense of them.
- Headache: This is the most common symptom of Chiari malformation. The headache is often pressure like and usually begins in the back of the head often radiates behind the eyes. Coughing, laughing, bending forward, sneezing or looking up can worsen the headache. Headache may be confused with migraine.
- Neck Pain: often pressure like and radiating down the spine and across the shoulders, Dizziness/vertigo, which often worsened by extension of the neck, vague or unexplained pains throughout the body, impaired balance, clumsiness, Chronic nausea, Foggy thinking, or poor memory and concentration, frequent or urgent urination, Irritable bowel syndrome, Auditory Symptoms, such as ringing in the ears and decrease in the ability to hear or sensitivity to sounds, difficulty swallowing, Changes in the voice – This can include hoarseness or the inability to regulate the voice when shouting or singing.
- Visual Symptoms: Including double vision, sensitivity to light, blind spots.
Types of Chiari Malformation (CM)
Type I involves the extension of the cerebellar tonsils (the lower part of the cerebellum) into the foramen magnum. There are usually no other associated malformations of the brain. This is the only form of Chiari malformation to present in adult life.
Type II involves the extension of both, the cerebellum and the brainstem tissue into the foramen magnum. Type II is always accompanied by a Myelomeningocele which is a severe form of spina bifida and is diagnosed at birth.
Type III is the most serious form of CM. It is quite rare and involves the protrusion or herniation of the hind part of the brain through a defect in the skull. This diagnosis is also evident at birth. Some people describe a Chiari 0 malformation, and are simply a Chiari I malformation in which the cerebellar tonsils do not protrude by the standard 5 mm. These are the patients that are frequently misdiagnosed because of the failure of the current diagnostic criteria to accurately reflect the underlying neurological problem.
The diagnostic process begins with Dr. Moza, a Simi Valley neurosurgeon, taking a complete medical history and performing a physical examination. He then follows this process up by a complete neurological evaluation that will allow him to assess your specific symptoms and neurological functioning. The patient with a Chiari 1 malformation may have an entirely normal examination. In such cases, it becomes more difficult to determine if Chiari is indeed the problem and if surgery is indeed the best solution. In such cases, the judgment of an experienced neurosurgeon becomes very important. When the neurological examination is abnormal, the pattern of abnormal findings can make it very easy to pinpoint the problem to the cervical spinal cord and brain stem. Patients may have difficulty with coordination, balance, eye movements, sensation and strength. The reflexes may be too active or not active enough. Reflexes that are never present except when the spinal cord is not functioning normally- pathological reflexes- may also be detected. MRI (Magnetic Resonance Imaging) is the best diagnostic tool for detecting Chiari malformation. This test provides the doctor with detailed anatomical information regarding the structures at the base of the brain. The criteria for diagnosing a Chiari malformation however have been very arbitrarily determined. This results in some doctors adhering to rigid standards – 5mm of tonsil herniation- before making the diagnosis of Chiari, even in the face of typical patient symptoms and obvious neurological findings. Hence many patients with Chiari go undiagnosed and untreated for years.
Some patients with Chiari malformation do not present with symptoms, therefore they do not require any form of treatment. Some symptoms of Chiari malformation, such as headache and dizziness may be effectively treated by medication. Medication alone, however, will not correct the root cause of the symptoms: the brain stem compression. As a rule, when the Chiari malformation causes symptoms that seriously impair the patient’s quality of life, it is best to consider surgery. Surgery for Chiari malformation is basically about creating more room for the brain. Surgery relieves compression of the brain stem and spinal cord and improves circulation of the spinal fluid.