**What is Craniopharyngioma?**
It is a slow growing, benign tumor that develops near the pituitary gland from embryonic tissue. This tumor is rare and generally affects children between the ages of 5 and 10. It is possible for an adult to be affected by this condition, but is uncommon. This specific tumor tends to disrupt the development of the skull completely and places stress on the pituitary gland, resulting in increasing pressure on the brain.
**Symptoms**
Symptoms tend to differ with age. Some of the most noticeable are: headaches, nausea, vomiting, delayed development in children, disruption in the proper function of the pituitary gland, and sometimes can affect the optic nerve. With disruption in the pituitary gland many children have hormone imbalances. This can lead to extreme thirst and urination abnormalities. The optic nerve damage can lead to vision problems and sometimes blindness. Symptoms that occur from Craniopharyngioma are often permanent and require surgery.
**Treatment**
The main treatment suggested by physicians to patients with Craniopharyngioma is surgery. In some cases the entire tumor is removed and in other patients on a portion of the tumor can be removed. Another choice that patients can choose is radiation therapy. This is the most recent treatment being utilized, but since it generally affects patients between the ages of 5 to 10 it is not always recommended.
**Prognosis**
After surgery, most patients can have about an 80% full recovery. There is a possibility of complete recovery if the entire tumor can be removed. The damage to the pituitary gland and optic nerve generally never completely heal and the patient can still experience hormone imbalances and often times vision problems even after surgery. In some cases these problems can become worse after surgery.
CT scan of the brain showing a craniopharyngioma (white structure in the center of the image).
www.medgle.es
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