Adults with CM may complain of:
As an infant, the child may have failure to thrive, gastroesophageal reflux, may not be sitting by six to seven months, or not walking by about 14-15 months. Older children may have headaches, dizziness, ringing in ears, problems with vision. One of the most frequent presentations is scoliosis with infrequent headaches, and no other symptoms.
Generally, an MRI is the preferred diagnostic test to determine if a cerebellar herniation exists. CT and traditional X-ray is also used, but are not as effective at diagnosing CM.
Surgical treatment to correct the compression involves removing a portion of the skull and usually part of the C1 vertebra. At this point the covering of the brain (dura) will likely be opened and a patch of similar material sewn in to make this covering (or dura) larger. The cerebellar tonsils may also be removed. This is done to return the flow of spinal fluid which relieves some or all of the symptoms as pressure is removed from the brain stem. This usually leads to shrinkage of any syrinx (spinal fluid) that might exist. The surgical procedure frequently keeps symptoms from getting worse or coming back.
For adults, some choose to manage their symptoms without surgery until if and when their symptoms become intolerable. Nearly 100% of the time patients who noted headaches as their symptoms improved. It is important to recognize that the size of the herniation of the brain (in millimeters) into the spine is not as important as the symptoms the patient experiences when deciding if surgery is an option.