Unlike many benign tumors, craniopharyngiomas in children require specialized treatment due to their location and relationship to deep structures in the head. Pediatric specialists at Children's Health are experienced in treating craniopharyngiomas and can guide you through a variety of treatment options. Symptoms of craniopharyngioma may be present at any age, and can range from pain to vision problems.
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The most common craniopharyngioma in children occurs in children between the ages of five and 14 years, although they can affect people of any age. The first step in treatment is surgery to remove the tumor. Your child may need to have a temporary hole cut in the skull or nose to allow the surgeon to perform the surgery. If the tumor is invading the brain, the surgeon may also need to place a drain tube. Radiation therapy is often necessary for children with hydrocephalus.
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Some craniopharyngiomas can be difficult to detect in the early stages of growth. The presence of an intracranial mass can affect the head's growth pattern. If a child has a enlarged head, this is an indication that an intracranial mass is present. Patients may experience blurred vision or complete loss of vision in some areas of their visual field. They should contact their physician if they suspect this condition.
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Thankfully, craniopharyngiomas can be treated. Surgical removal of the tumor is typically an option. If the tumor has spread, high doses of radiation may be required. While most people are cured, some of the tumors may recur. The risk of recurrence is very high, but if the tumor is removed completely, it will not cause any lasting damage to the attached tissue.
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If the tumor is causing problems, it may be a sign of craniopharyngioma. The tumor is usually benign and will not spread. However, it can be painful for children. While a tumor in the head can be a sign of a craniopharyngioma, it is not cancerous. Its main characteristic is that it is attached to critical structures in the brain.
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The earliest symptom of craniopharyngioma in children is a dilated skull. A swelling in the head, enlarged circumference, and abnormalities in the eyes are signs of craniopharyngioma. During a surgical procedure, the tumor can be removed. It is a surgical procedure that requires multiple incisions and can be performed in a variety of ways.
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Symptoms of craniopharyngioma in childhood vary in severity. Most children are diagnosed at an early age, but a diagnosis of craniopharyngioma can be delayed until the child reaches the age of majority. Regardless of how severe the disease is, the symptoms of craniopharyngioma are usually similar to those of other types of tumors.
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The most common type of craniopharyngioma in children is adamantinomatous craniopharyngioma, which has a layered appearance and a high degree of calcium. A child with this type of tumor is most likely to experience cysts and calcium buildup. Papillary craniopharyngiomas are rare in children, but are still treatable with surgery.
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Most children with craniopharyngioma will have some symptoms for years before they are diagnosed. Their symptoms will include headaches, endocrine and visual changes, and the presence of a tumor in the cranium. They may also affect their growth patterns. The symptoms of craniopharyngioma in childhood are usually mild or non-existent. While craniopharyngioma in children is largely benign, they may interfere with normal development in the child.
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The symptoms of craniopharyngioma in childhood include the following: a recurring tumor or a new one. The location of the tumor may cause problems with the child's development and behavior. A child may have a tendency to develop this tumor, or it may develop during an early or delayed puberty. MRI of the brain will help determine the correct diagnosis. Once it has been confirmed, the tumor will be removed using a combination of radiosurgery and chemotherapy.
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In addition to being a nuisance, craniopharyngioma in childhood can affect a child's health. It may affect the child's ability to grow and develop properly. Symptoms of this tumor in children can be asymptomatic or cause a deterioration of vision. It is essential to seek a specialist for diagnosis and treatment. This can be a life-threatening condition.