The short answer
Brain and other central nervous system (CNS) tumors are the second most common group of cancers in children. They include many different types, and treatment may involve surgery, radiation, and chemotherapy depending on the tumor's type and location.
Brain and CNS tumors are the second most common childhood cancer group, after leukemias.
There are many different types, named for the cells they start in and where they grow.
Symptoms depend on the tumor's location and can include headaches, nausea, balance problems, or seizures.
Treatment may combine surgery, radiation therapy, and chemotherapy.
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The full explanation.
The simple version
Brain tumors are among the most common childhood cancers, along with leukemia. A tumor that starts in the brain is called a primary brain tumor. Treatment and outlook vary a lot by tumor type. Getting the exact diagnosis matters as much as knowing it is a brain tumor at all.
Common types in children
Medulloblastoma is one of the most common childhood brain tumors. It grows in the cerebellum, the part of the brain that controls balance and coordination. Gliomas, including astrocytomas, grow from the brain's supporting cells. They can be low-grade, meaning slower growing, or high-grade, meaning faster growing. Ependymomas grow from cells that line the fluid-filled spaces in the brain and spinal cord.
Diffuse intrinsic pontine glioma, often called DIPG, grows in the brainstem. This is the part of the brain that controls breathing and heartbeat. Its location makes DIPG especially hard to treat. Craniopharyngioma grows near the pituitary gland, the gland that controls many of the body's hormones.
Signs to watch for
Signs depend on where the tumor is and how old your child is. Common signs include morning headaches, vomiting without feeling sick to the stomach, new problems with balance, vision changes, seizures, or a change in behavior or grades at school. In babies, a rapidly growing head size can be a sign, since a baby's skull can still expand. Any of these signs deserves a prompt doctor visit. This is especially true if more than one sign appears together, or a headache keeps getting worse.
How doctors diagnose it
An MRI is usually the main test. It shows the brain and spinal cord in detail. A biopsy, or surgery to remove part or all of the tumor, lets doctors examine the tissue directly. This tells them the exact tumor type. It can also reveal specific gene changes inside the tumor. That genetic information can guide treatment choices, and sometimes points toward a clinical trial.
How it is treated
Treatment depends on the tumor type, its location, and your child's age. When the tumor's location allows it, surgery to remove as much of it as safely possible is often the first step. Radiation therapy is used for some tumors. Doctors try to limit radiation in very young children, because of its effect on a still-developing brain. Chemotherapy is used for many tumor types. Sometimes it comes before surgery, to shrink the tumor. Sometimes it comes after. For some tumor types, newer targeted therapies aimed at specific gene changes are now part of standard treatment.
Clinical trials and specialized centers
Childhood brain tumors are complex. Treatment at a children's cancer center with specific experience in pediatric brain tumors matters. Many centers offer clinical trials, including through the Children's Oncology Group and specialized brain tumor research networks. Ask whether a trial fits your child's exact tumor type.
Life after treatment
Recovery after a childhood brain tumor often includes rehabilitation: physical therapy, occupational therapy, or speech therapy, depending on what the tumor or its treatment affected. School support matters too. Many survivors benefit from an individualized education plan that adjusts pace, testing, or classroom support. Ask your child's team for a referral to rehabilitation services early, rather than waiting to see if problems appear on their own.
When to call the doctor right away
Call your child's care team, or go to the emergency room, for a sudden severe headache, repeated vomiting, a seizure, sudden trouble walking or talking, or a rapid change in alertness. These can be signs of pressure building inside the skull. That needs urgent evaluation, not a wait-and-see approach.
What to ask your child's team
Ask for the exact tumor type, and its genetic features if known. Ask what surgery, radiation, or chemotherapy is planned, and why. Ask about a clinical trial. Ask what long-term follow-up will look like. Brain tumor treatment carries a higher chance of late effects on learning, hormones, and growth, so ask what your child's team will be watching for over time.
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Words to know
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Common questions
How common are brain tumors in children?
Brain and other central nervous system (CNS) tumors are the second most common group of cancers in children, after leukemias.
Are there different kinds?
Yes. There are many types of childhood brain and spinal cord tumors, named for the cells they begin in and the part of the CNS where they grow. Examples include gliomas, medulloblastomas, and ependymomas.
What are the symptoms?
Symptoms depend on where the tumor is. They can include morning headaches, nausea or vomiting, balance or coordination problems, vision changes, or seizures.
How are they treated?
Treatment depends on the type and location and may include surgery, radiation therapy, and chemotherapy, sometimes in combination.
Who treats childhood brain tumors?
Care is led by pediatric specialists — such as pediatric neurosurgeons, neuro-oncologists, and radiation oncologists — usually at a children's cancer center.
Questions to ask your doctor
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Last updated: 2026-08-18Next planned review: 2027-07-07
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How this page was created
Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes. We do not employ clinicians and do not intend to — our work is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.
Editorial status: Source checked — This page was written with AI assistance and checked line by line against the sources listed on it. That confirms the sources support what the page says. It is not a medical review, and it does not confirm the page is complete or right for your situation.
Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.
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