The majority of brain tumors have abnormalities of genes involved in cell cycle control, causing uncontrolled cell growth. These abnormalities are caused by alterations directly in the genes, or by chromosome rearrangements which change the function of a gene.

Patients with certain genetic conditions (i.e. neurofibromatosis, von Hippel-Lindau disease, Li-Frameni syndrome and retinoblastoma) also have an increased risk to develop tumors of the central nervous system. There have also been some reports of children in the same family developing brain tumors who do not have any of these genetic syndromes.

Research has been investigating parents of children with brain tumors and their past exposure to certain chemicals. Some chemicals may change the structure of a gene that protects the body from diseases and cancer. Workers in oil refining, rubber manufacturing and chemists have a higher incidence of certain types of tumors. Which, if any, chemical toxin is related to this increase in tumors is unknown.

Children who have received radiation therapy to the head as part of prior treatment for other malignancies are also at an increased risk for new brain tumors.

The following are the most common symptoms of a brain tumor. However, each child may experience symptoms differently. Symptoms vary depending on size and location of tumor. Many symptoms are related to an increase in pressure in or around the brain. There is no spare space in the skull for anything except the delicate tissues of the brain and its fluid. Any tumor, extra tissue, or fluid can cause pressure on the brain and result in the following symptoms:

• Increased intracranial pressure (ICP) - caused by extra tissue or fluid in the brain. Pressure may increase because one or more of the ventricles that drain cerebrospinal fluid (CSF, the fluid that surrounds the brain and spinal cord) has been blocked, causing the fluid to be trapped in the brain. Increased ICP can cause the following:
  • Headache
  • Nausea
  • Personality changes
  • Irritability
  • Drowsiness
  • Depression
  • Decreased cardiac and respiratory function and eventually coma if not treated

Symptoms vary depending upon which part of the brain the tumor is found. Symptoms of brain tumors in the cerebrum (front of brain) may include:

• Seizures
• Visual changes
• Slurred speech
• Paralysis or weakness on half of the body or face
• Increased intracranial pressure (ICP)
• Drowsiness or confusion
• Personality changes

Symptoms of brain tumors in the brainstem (middle of brain) may include:

• Seizures
• Endocrine problems (diabetes or hormone regulation)
• Visual changes or double vision
• Headaches
• Paralysis of nerves/muscles of the face or half of the body
• Respiratory changes
• Increased intracranial pressure (ICP)

Symptoms of brain tumors in the cerebellum (back of brain) may include:

• Increased intracranial pressure (ICP)
• Vomiting (usually occurs in the morning without nausea)
• Headache
• Uncoordinated muscle movements
• Problems walking (ataxia)

The symptoms of a brain tumor may resemble other conditions or medical problems. Always consult your child's physician for a diagnosis.

The different types of brain tumors include the following: 

• Gliomas

The most common type of brain tumor is a glioma. Gliomas begin from glial cells, which are the supportive tissue of the brain. There are several types of gliomas, categorized by where they are found and the type of cells that originated the tumor. The following are the different types of gliomas:

• Astrocytomas

Astrocytomas are glial cell tumors that are derived from connective tissue cells called astrocytes. These cells can be found anywhere in the brain or spinal cord. Astrocytomas are the most common type of childhood brain tumor. Astrocytomas are generally subdivided into high-grade or low-grade tumors. High-grade astrocytomas are the most malignant of all brain tumors. Astrocytomas are further classified for presenting signs, symptoms, treatment and prognosis, based on the location of the tumor. The most common location of these tumors is in the cerebellum, where they are called cerebellar astrocytomas. These persons usually have symptoms of increased intracranial pressure, headache and vomiting. There can also be problems with walking and coordination, as well as double vision.

• Brain stem gliomas

Brain stem gliomas are tumors found in the brain stem. Most brain stem tumors cannot be surgically removed because of the remote location and delicate and complex function this area controls. Brain stem gliomas occur almost exclusively in children; the group most often affected is the school-age child. The child usually does not have increased intracranial pressure, but may have problems with double vision, movement of the face or one side of the body or difficulty with walking and coordination.

• Ependymomas

Ependymomas are also glial cell tumors. They usually develop in the lining of the ventricles or in the spinal cord. The most common place they are found in children is near the cerebellum. The tumor often blocks the flow of the CSF (cerebral spinal fluid, which bathes the brain and spinal cord), causing increased intracranial pressure. This type of tumor mostly occurs in children younger than 10 years of age. Ependymomas can be slow growing, compared to other brain tumors, but may recur after treatment is completed. Recurrence of ependymomas results in a more invasive tumor with more resistance to treatment.

• Optic nerve gliomas

Optic nerve gliomas are found in or around the nerves that send messages from the eyes to the brain. They are frequently found in persons who have neurofibromatosis, a condition a child is born with that makes the child more likely to develop tumors in the brain. Persons usually experience loss of vision, as well as hormone problems, since these tumors are usually located at the base of the brain where hormonal control is located. These are typically difficult to treat due to the surrounding sensitive brain structures.

• Primitive neuroectodermal tumors (PNET)

PNET can occur anywhere in the brain of a child, although the most common place is in the back of the brain near the cerebellum. When they occur here, they are called medulloblastomas. The symptoms depend on their location in the brain, but typically the child experiences increased intracranial pressure. These tumors are fast growing and often malignant, with occasional spreading throughout the brain or spinal cord.

• Medulloblastomas

Medulloblastomas are one type of PNET that are found near the midline of the cerebellum. This tumor is rapidly growing and often blocks drainage of the CSF (cerebral spinal fluid, which bathes the brain and spinal cord), causing symptoms associated with increased ICP. Medulloblastoma cells can spread (metastasize) to other areas of the central nervous system, especially around the spinal cord. A combination of surgery, radiation and chemotherapy is usually needed to control these tumors.

• Craniopharyngioma

Craniopharyngioma are benign tumors that occur at the base of the brain near the nerves from the eyes to the brain and the hormone centers. Most persons with this type of brain tumor develop symptoms before the age of 20. Symptoms include headaches, as well as problems with vision. Hormonal imbalances are common, including poor growth and short stature. Symptoms of increased intracranial pressure may also be seen. Although these tumors are benign, they are hard to remove due to the sensitive brain structures that surround them.

• Pineal region tumors

Many different tumors can arise near the pineal gland, a gland which helps control sleep and wake cycles. Gliomas are common in this region, as are pineal blastomas (PNET). In addition, germ cell tumors, another form of malignant tumor, can be found in this area. Tumors in this region are more common in children than adults and make up 3 to 8 percent of pediatric brain tumors. Benign pineal gland cysts are also seen in this location, which makes the diagnosis difficult between what is malignant and what is benign. Biopsy or removal of the tumor is frequently necessary to tell the different types of tumors apart. Persons with tumors in this region frequently experience headaches or symptoms of increased intracranial pressure. Treatment depends on the tumor type and size.

Treatment for brain tumors

Specific treatment for brain tumors will be determined by your child's physician based on:

• Your child's age, overall health and medical history

• Type, location, and size of the tumor

• Extent of the disease

• Your child's tolerance for specific medications, procedures or therapies

• Expectations for the course of the disease

• Your opinion or preference

Treatment for brain tumors may include (alone or in combination)

• Surgery - Surgery is usually the first step in the treatment of brain tumors. The goal is to remove as much of the tumor as possible while maintaining neurological function. Surgery for a biopsy is also done to examine the types of cells the tumor is made of for a diagnosis. This is frequently done if the tumor is in an area with sensitive structures around it that may be injured during removal.

• Chemotherapy

• Radiation therapy

• Steroids (to treat and prevent swelling especially in the brain)

• Anti-seizure medication (to treat and prevent seizures associated with intracranial pressure)

• Ventriculoperitoneal shunt (Also called a VP shunt) - A VP shunt may be placed in the head to drain excess fluid from inside the brain. A VP shunt helps control the pressure inside the brain

• Lumbar puncture/spinal tap (to test pressure in the central nervous system, to look for suspicious cells, and give medication if needed)

• Bone marrow transplantation

• Supportive care (for the side effects of the tumor or treatment)

• Rehabilitation (to regain lost motor skills and muscle strength; speech, physical and occupational therapists may be involved in the healthcare team)

• Antibiotics (to treat and prevent infections)

• Continuous follow-up care (to manage disease, detect recurrence of the tumor and to manage late effects of treatment)

Long-term outlook for a child with a brain tumor:

Prognosis greatly depends on:

• The type of tumor

• The extent of the disease

• Size and location of the tumor

• Presence or absence of metastasis

• The tumor's response to therapy

• The age and overall health of your child

• Your child's tolerance of specific medications, procedures or therapies

• New developments in treatment

As with any cancer, prognosis and long-term survival can vary greatly from individual to individual. Prompt medical attention and aggressive therapy are important for the best prognosis. Continuous follow-up care is essential for a child diagnosed with a brain tumor. Side effects of radiation and chemotherapy, as well as second malignancies, can occur in survivors of brain tumors.

Rehabilitation for lost motor skill and muscle strength may be required for an extended amount of time. Speech therapists and physical and occupational therapists may be involved in some form of rehabilitation. More research is needed to improve treatment, decrease side effects of the treatment for this disease and develop a cure. New methods are continually being discovered to improve treatment and to decrease side effects.