Neuroblastoma is a type of cancer that starts in nerve tissue, most often in children under five. It can appear in the adrenal glands, neck, chest or pelvis. Because it grows fast, spotting it early makes a big difference.
If your child has an unexplained lump that feels firm under the skin, especially near the abdomen, think about neuroblastoma. Other red flags include persistent pain, fever without infection, loss of appetite, or unusual bruising. Some kids develop a hoarse voice or trouble breathing if the tumor presses on nearby organs.
These signs can look like everyday kid illnesses, so it’s easy to miss them. The rule of thumb: if a lump doesn’t go away in a couple of weeks, or symptoms get worse, call your pediatrician right away.
Doctors decide on treatment based on where the tumor is, how big it’s grown and whether it has spread. Surgery to remove the mass is often the first step if the tumor is accessible. When surgery alone isn’t enough, chemotherapy helps shrink the cancer cells.
Radiation therapy may be used after surgery or chemo to target any leftover cells. In recent years, immunotherapy—drugs that help the immune system recognize and attack neuroblastoma—has shown promising results for high‑risk cases.
High‑risk neuroblastoma sometimes needs a combination of all three approaches plus stem cell transplant. While it sounds intense, many children respond well and go on to live normal lives.
Side effects vary: chemo can cause hair loss and nausea, radiation may affect growth in the treated area, and immunotherapy can lead to flu‑like symptoms. Your medical team will monitor these closely and adjust doses as needed.
Support isn’t just about medicine. Nutrition, physical therapy and counseling help kids cope with treatment fatigue and emotional stress. Joining a support group connects families with others who understand the daily challenges.
If you suspect neuroblastoma, ask your doctor for imaging tests like ultrasound, MRI or CT scans. A biopsy—taking a tiny piece of tissue—confirms the diagnosis under a microscope. Blood and urine tests can also reveal markers that indicate neuroblastoma activity.
After treatment, regular follow‑up visits track growth, check for recurrence and manage any long‑term effects. Survivorship plans often include heart checks, hormonal evaluations and educational support.
Facing neuroblastoma is scary, but knowing the signs, diagnosis steps and treatment options gives you a stronger footing. Talk openly with your child’s doctors, ask about clinical trials if eligible, and lean on family or community resources for extra help.
Remember: early detection, a clear treatment plan and solid support can turn a tough diagnosis into a manageable journey.