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Craniopharyngioma in Childhood Symptoms - Oren Zarif - Craniopharyngioma in Childhood


Most craniopharyngioma in children has no specific symptoms, but the patient may have problems feeding and communicating. These symptoms may be related to pressure placed on the brain by the growing tumor. Treatment involves removal of the tumor through surgery. This procedure may involve cutting the skull or opening the upper lip. After surgery, radiation therapy can help shrink the tumor. However, there are other possible causes of these symptoms.

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The cause of craniopharyngioma in children is unknown, but it is believed to develop during the child's brain development. It is believed to form near the pituitary gland, which secretes hormones that control many body functions. Because the tumor is so close to the pituitary gland, it can interfere with the function of the pituitary gland and surrounding structures in the brain. Most cases of craniopharyngioma are benign, but some people will develop these symptoms as they grow older.

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If you think you may be experiencing some of these symptoms, you should see a doctor. While craniopharyngiomas are typically benign, they can be large and can put pressure on various areas of the brain. In addition to causing pain, a craniopharyngioma can also affect a child's growth and hormone levels. A child may have delayed or early puberty, as well as obesity.

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Most craniopharyngioma in childhood affects children between 5 and 14 years of age. They can affect children of any age. If they are diagnosed with craniopharyngioma in Childhood, the doctor will perform surgery to remove the tumor. This surgery may involve a temporary hole in the skull or nose. The surgeon may place a drain tube during the surgery to remove any excess water. If the child is suffering from hydrocephalus, radiation therapy may be recommended.

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Symptoms of craniopharyngioma in childhood include visual changes, endocrine changes, and headaches. These conditions are associated with pressure on different parts of the brain, including the hypothalamus, cerebellum, and the cerebrospinal fluid pathways. Patients may also experience other symptoms, such as nausea and vomiting. In addition, they may develop a fever and exhibit signs of depression, irritability, and agitation.

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There are two main types of craniopharyngioma in childhood. Those that affect the brain's pituitary gland and may be affected by vision and hormones. Other kinds of children may show endocrine changes, which can include headaches. Other symptoms of craniopharyngioma include endocrine changes, visual problems, and hearing loss.

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Although most craniopharyngiomas are benign, they can have adverse effects on vision. A child may have a decreased ability to hear or have problems swallowing food. A pediatrician will determine whether a child has symptoms related to the tumor. The symptoms of craniopharyngioma in childhood may be a result of a genetic predisposition to the condition. If your child has these symptoms, you should seek immediate treatment.

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In children, the symptoms of craniopharyngioma may include seizures, vision loss, and hearing loss. The child may have a symptom or two, but a diagnosis is not necessary for a diagnosis. If your child has been diagnosed with craniopharyngioma, you should schedule an appointment with a pediatrician. During this appointment, your doctor will evaluate the size of the tumor and the location of the tumor.

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The symptoms of craniopharyngioma in childhood include: a headache and hearing loss. The tumor can cause a child to lose vision in certain areas of the visual field. The tumor can also cause the child to have difficulty speaking or eating. Those with visual problems should seek immediate treatment for craniopharyngioma in children. In many cases, these are symptomatic of other diseases.

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The most common symptom of craniopharyngioma is a lump in the brain that can be removed with surgery. The symptoms of craniopharyngioma in childhood may be asymptomatic and will resolve with treatment. Some craniopharyngiomas contain cysts, which may require removal. This type of tumor does not affect vision or growth.

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