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Tests for Neuroblastoma

Neuroblastomas are usually found when a child is brought to the doctor because they are having signs or symptoms. If a neuroblastoma (or another type of tumor) is suspected, tests will be needed to confirm the diagnosis.

If a neuroblastoma is found, other tests will be needed to learn more about it.

Medical history and physical exam

If your child has signs or symptoms that might be caused by neuroblastoma (or another tumor), the doctor will ask about the symptoms and how long they have been present. The doctor might also ask if there are any possible risk factors for developing neuroblastoma, such as a family history.

The doctor will examine your child for possible signs of neuroblastoma or other health problems. The exam may include vital signs (temperature, heart rate, blood pressure), and checking the skin, eyes, neck, chest and abdomen (belly) for any bruises, lumps, or other abnormal findings. They may ask your child to walk or perform tests to check their muscle strength. These tests are meant to find out what is going on with your child and understand the cause of your child’s symptoms.

Some signs that could be caused by neuroblastoma, such as fever and enlarged lymph nodes, are much more likely to be caused by an infection, so the doctor might look for other signs of infection at first.

If the medical history and exam suggest a child might have neuroblastoma (or another type of tumor), more tests will be done. These could include:

  • Blood and urine tests
  • Imaging tests
  • Biopsies

These tests are important because many of the symptoms and signs of neuroblastoma can also be caused by other diseases, such as infections, or even other types of cancer.

Blood and urine catecholamine tests

Cells in the body make many different types of hormones. For example, sympathetic nerve cells normally release hormones called catecholamines, such as epinephrine (adrenaline) and norepinephrine, which enter the blood and eventually break down into smaller pieces, called metabolites. The metabolites normally pass out of the body in urine. When epinephrine and norepinephrine are broken down, the two most common metabolites made are:

  • Homovanillic acid (HVA)
  • Vanillylmandelic acid (VMA)

Neuroblastoma cells also often make these catecholamines, so these same metabolites can be detected in blood and urine. If the neuroblastoma cells are making catecholamines, the amount of HVA and VMA in urine or blood will be higher than expected.

If a child does have neuroblastoma and levels of HVA and VMA are elevated at diagnosis, these tests can also be followed during treatment to get an idea of how well treatment is working.

Other blood and urine tests: If neuroblastoma is suspected or has been found, your child’s doctor will probably order blood tests to check blood cell counts, liver and kidney function, and the balance of salts (electrolytes) in the body. A urinalysis (urine test) may also be done to help check kidney function.

Imaging tests

Imaging tests are used to create pictures of the inside of the body. Imaging tests can be done for a number of reasons, including:

  • To help find out if a suspicious area might be cancer
  • To learn how far cancer has spread
  • To help determine if treatment is working

Most children who have or might have neuroblastoma will get one or more of these tests, but they might not need all of them.

Children with neuroblastoma are often very young, so it can be hard to do some of these tests. Depending on the child's age and the imaging test being done, they might get medicines to help them stay still or go to sleep.

Ultrasound uses sound waves and their echoes to look inside the body. This might be one of the first tests done in very young children if a tumor is suspected. It is fairly quick and easy, it does not use radiation, and it can often give the doctor a good view inside the body.

Ultrasound is used most often to look for tumors in the abdomen.

MRI scans provide detailed images of soft tissues in the body. These scans may be slightly better than CT scans for seeing a neuroblastoma tumor, especially around the spine.

MRI scans use radio waves and strong magnets to create the images instead of x-rays, so there is no radiation. A contrast material called gadolinium may be injected into a vein before the scan to better see details.

CT scans combine many x-ray pictures to make detailed cross-sectional images of the inside of the body. These tests are often used to look for neuroblastoma in the abdomen, pelvis, and chest.

Before the test, your child may be asked to drink a contrast solution and/or get an IV (intravenous) injection of a contrast dye. These medicines can be used to get a clearer picture.

CT-guided core needle biopsy: CT scans can also be used to help guide a biopsy needle into a tumor, although this is not often done for children with neuroblastoma.

This test is often an important part of finding out how far a child's neuroblastoma has spread. It may be done after a CT scan or MRI.

For this test, a form of the chemical meta-iodobenzylguanidine (MIBG) that contains a small amount of radioactive iodine is injected into the vein. MIBG is similar to norepinephrine, a hormone made by sympathetic nerve cells. In most children, it will attach to neuroblastoma cells anywhere in the body. Between 1 and 3 days later, the body is scanned with a special camera to look for areas that picked up the radioactivity. This helps doctors know where neuroblastoma is and if it has spread to the bones and/or other parts of the body.

MIBG scans can be repeated after treatment to see if the tumors are responding well. It is also good to know if the tumor takes up the MIBG because in some cases, this radioactive molecule can be used at higher doses to treat the neuroblastoma (see Radiation Therapy for Neuroblastoma).

To protect the thyroid gland, a medicine containing non-radioactive iodine is given before, during, and after the test.

If your child’s doctor thinks neuroblastoma is affecting the bone but an MIBG scan does not show this, sometimes a PET scan can be done to be sure (see below).

For a PET scan, a radioactive substance (usually a type of sugar called FDG) is injected into the blood. The amount of radioactivity used is very low and will pass out of the body within a day or so. Because cancer cells are growing quickly, they absorb large amounts of the radioactive sugar.

After about an hour, your child will be moved onto a table in the PET scanner. They will lie on the table for about 30 minutes while a special camera creates a picture of areas of radioactivity in the body. Younger children may be given medicine to help them stay calm or even sleep during the test.

PET scans are usually not needed if an MIBG scan has been done. But a PET scan might be useful for some neuroblastomas, especially if there is no uptake of MIBG in the neuroblastoma cells.

X-rays can be used to look at the bones, although they are not as good at showing other structures in the body.

The doctor may order an x-ray if a child is having symptoms and it is not clear what might be causing them. But the pictures might not be good enough to spot tumors.

In children with neuroblastoma, a MIBG, PET, or bone scan is usually better than an x-ray for looking at the bones in the rest of the body and to see if neuroblastoma has spread to the bones, but an x-ray test might still be helpful in some situations.

Biopsies

During a biopsy, a doctor removes one or more pieces from the tumor for testing.

Exams and imaging tests might strongly suggest a child has neuroblastoma, but a biopsy is often needed to be sure. If it is neuroblastoma, lab tests can also help determine how quickly the tumor might grow or spread, as well as which treatments might work best. 

In adults, biopsies are sometimes done using local anesthetic (numbing medicine), but in children they are more often done while the child is under general anesthesia (asleep).

Some very young infants with small adrenal tumors seen on an imaging test might not need a biopsy. Instead, the tumor might be watched closely with more imaging tests over time, as these tumors can mature or go away on their own.

Surgical biopsy is the most common type of biopsy for neuroblastoma. It is done by removing a piece of the tumor through an incision (cut) in the skin. For tumors deep in the body, this may be done laparoscopically using long, thin surgical tools inserted through small cuts in the skin. A surgical biopsy is most often used in the diagnosis of neuroblastoma.

For this type of biopsy, a thin, hollow needle is inserted through the skin and into the tumor to remove a small sample. If the tumor is deep within the body, CT scans or ultrasound can be used to help guide the needle into the tumor. This type of biopsy is less common for children with suspected neuroblastoma.

Neuroblastoma can spread to the bone marrow (the soft inner parts of certain bones). If blood or urine levels of catecholamines are increased, then finding cancer cells in a bone marrow sample is enough to diagnose neuroblastoma (without getting a biopsy of the main tumor). If neuroblastoma has already been diagnosed by a biopsy done elsewhere in the body, bone marrow tests are done to help determine the extent of the disease.

A bone marrow aspiration and biopsy are usually done at the same time. Samples are taken from the hip bones.

Even when the area is numbed with local anesthetic, these tests can be painful, so in most cases, the child is also given other medicines to reduce pain or go to sleep during the procedure.

For a bone marrow aspiration, a thin, hollow needle is inserted into the bone and a syringe is used to suck out a small amount of liquid bone marrow.

For a bone marrow biopsy, small pieces of bone and marrow are removed by placing a slightly larger needle in the bone. Once the biopsy is done, pressure is applied to the site to help stop any bleeding.

Samples from the bone marrow are sent to a lab, where they are looked at and tested for the presence of cancer cells. You can read more about testing tissue samples in Testing Biopsy and Cytology Specimens for Cancer.

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Developed by the American Cancer Society medical and editorial content team with medical review and contribution by the American Society of Clinical Oncology (ASCO).

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National Cancer Institute. Neuroblastoma Treatment (PDQ). 2024. Accessed at https://www.cancer.gov/types/neuroblastoma/hp/neuroblastoma-treatment-pdq on March 24, 2025.

Park JR, Hogarty MD, Bagatell R, et al. Chapter 23: Neuroblastoma. In: Blaney SM, Adamson PC, Helman LJ, eds. Pizzo and Poplack’s Principles and Practice of Pediatric Oncology. 8th ed. Philadelphia Pa: Lippincott Williams & Wilkins; 2021.

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Last Revised: June 26, 2025

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