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Symptoms of Craniopharyngioma in Childhood - Oren Zarif - Craniopharyngioma in Childhood

  • Writer: Oren Zarif
    Oren Zarif
  • Mar 23, 2022
  • 3 min read

Children with symptoms of craniopharyngioma are generally diagnosed as being at-risk for the tumor. This type of cancer usually develops at an early age. The exact cause of the condition is unknown, but scientists have hypothesized that it can develop during the brain development process. Treatment will vary depending on the size of the tumor and its location in the body. Doctors will ask about the child's symptoms and chart their height and weight. The doctor will look for changes in their growth patterns.

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While most craniopharyngiomas occur in children, they can occur at any age. If your child has any of these symptoms, it is best to visit a physician immediately. The first step in treatment is removal of the tumor, which the surgeon may do through a temporary hole in the skull or a hole in the nose. If the tumor has filled with fluid, the surgeon may put a drain tube into the child's brain. Radiation therapy may also be necessary.

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A patient may have cognitive and behavioral problems. About 50% of patients experience headaches, but they may be due to increased intracranial pressure or to meningeal irritation caused by the cystic fluid. About 10% of patients develop seizures. About 50% of children with craniopharyngioma present with visual symptoms. The most common visual disturbance is optic chiasm compression or temporal hemianopsia. In severe cases, the child may have water in the brain. In addition to surgery, the child may also be prescribed radiation therapy to treat the hydrocephalus.

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The signs and symptoms of craniopharyngioma in childhood include visual changes, endocrine changes, and headaches. These tumors press on surrounding brain structures, causing symptoms that interfere with the brain's function. A patient's growth, vision, and hormone production are affected by a craniopharyngioma. These tumors can affect a child's growth and development.

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Symptoms of craniopharyngioma in childhood are similar to those of other childhood diseases. They will have a headache, but they can also include vision problems and breathing issues. Unlike other childhood conditions, craniopharyngiomas in childhood are benign and usually cause no lasting damage. They can be treated through radiotherapy or surgery, and they are usually cured within a year.

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The most common symptoms of craniopharyngioma in childhood include visual changes. Some patients will experience headaches, while others will only experience visual disturbances if the tumor has spread to the brain. Other symptoms of craniopharyngiomin in childhood will include hearing loss, vision loss, and hormonal changes. However, these are not the only signs of craniopharyngioma.

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Almost half of craniopharyngioma in childhood patients will experience headaches. The symptoms may be caused by increased intracranial pressure or meningeal irritation from the cystic fluid. In other cases, visual signs of craniopharyngioma will include a blurred or missing vision in some areas of the visual field. Most people with craniopharyngioma will have symptoms of fever, vomiting, and rash.

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In some cases, craniopharyngioma in childhood can be treated. In some cases, the tumor can be surgically removed. This procedure is usually performed to remove the tumor. This may cause damage to the surrounding tissues. In many cases, this treatment will result in a temporary solution. While it is not uncommon for the craniopharyngioma in Childhood to be removed, it is often not an effective treatment.

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Headaches and vision problems are common symptoms of craniopharyngioma. Some cases have been characterized by monoplegia or hemiplegia. In addition, about 5% of patients experience endocrine symptoms. Some patients may have vision changes and a calcified tumor. For these cases, surgery is the main treatment. If the tumor is still present in the brain, it is likely to be painful.

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The most common type of craniopharyngioma in childhood is an adenomatous tumor. While it is rare, it can cause life-threatening complications. The tumor may grow slowly or even appear suddenly, and may not be detected until it is pressing on important parts of the brain. Once diagnosed, a doctor will recommend treatment and monitor the growth of the tumor. It is important to seek treatment immediately to prevent further damage and recurrence.

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