Children's Health is the place to turn when you're dealing with craniopharyngioma in childhood. Our team of physicians has extensive experience treating these rare tumors and offers a variety of treatment options. Though most craniopharyngiomas are harmless, they can cause some problems due to their location and relationship to deep structures of the brain. Here are some of the symptoms you may encounter if you have a child with this disease.
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The most common craniopharyngiomas are located in the head and neck. They are benign tumors that do not spread to other areas. Surgical removal of the tumors is the only treatment for these conditions. While most children who have craniopharyngiomas survive, treatment for children depends on the type and location of the tumor. Your doctor may recommend radiation therapy or different types of surgery, depending on the severity of your child's symptoms.
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The most common symptoms of craniopharyngioma in children are vision changes, headaches, and calcium buildup. Patients with these tumors may also have vision changes. A physical and neurological exam will reveal the presence of these symptoms. The diagnosis is made when the child is five to 14 years old. The signs and symptoms of this cancer can be difficult to diagnose and may vary. The best way to diagnose craniopharyngioma in childhood is to visit your pediatrician and make sure that the tumor is located in the right place.
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Some patients have symptoms years before their diagnosis. These tumors can compress optic nerves or obstruct the cerebral spinal fluid pathway, which can result in blurred or even lost vision in certain areas of the visual field. People with visual symptoms are often diagnosed with craniopharyngioma in Childhood. Besides the above-mentioned symptoms, some children also develop a deficiency of thyroid hormones.
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A pediatric craniopharyngioma is a benign tumor that develops in the head of a baby. It can range in size, from a small, round lump to a large, solid mass. It can affect the brain's blood vessels and optic pathways. If the tumor is large, it can interfere with the functioning of important structures nearby. In children, the primary treatment for craniopharyngioma in childhood is surgery.
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The symptoms of craniopharyngioma in childhood include: headaches and seizures. About half of children with this tumor experience some type of headache. Other signs may include short stature and growth retardation. Although these symptoms may be temporary, they may indicate a larger problem in the future. In severe cases, the tumor can compress important anatomical structures. As a result, the patient may experience seizures and paresis.
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Symptoms of craniopharyngioma in childhood can vary. These include headache, increased intracranial pressure, and hydrocephalus. In a majority of cases, there are no symptoms of craniopharyngioma, though it may be present in some cases. However, if the tumor is located close to the pituitary gland, it will most likely cause a headache.
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The most common symptoms are ataxia and hydrocephalus. These can be associated with an endocrine abnormality, including growth retardation. While some craniopharyngioma symptoms are not life-threatening, they may result in complications later on in life. Moreover, they can affect the child's growth and development. When you notice any of these symptoms, you should consult a doctor immediately.
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Often, craniopharyngiomas may be asymptomatic, but the symptoms of this condition are sometimes present for years before diagnosis. The most obvious symptom of this condition is enlarged head circumference. It can also compress the pituitary stalk and the optic nerves. Increasing intracranial pressure may also result in papilledema. These symptoms are often caused by a tumor pressing on these areas of the brain.
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Treatment for craniopharyngioma in childhood depends on the age of the child, the location of the tumor, its size, and its location. Its treatment options vary widely and can result in vision and hormone dysfunction. The first step is surgery, which removes as much of the tumor as possible. If the tumor is not removed, it will be treated with radiation, either through focused radiation or a combination of treatments.