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Sacrococcygeal Teratoma

What is sacrococcygeal teratoma?

Sacrococcygeal GIG

SCT is a rare tumor that develops at the coccyx (tailbone) of the fetus. In most cases, these tumors are small and benign, and rarely present complications during pregnancy. However, SCT’s can grow during pregnancy and develop very large blood vessels. As a result, the fetal heart must do additional work by pumping blood through the tumor. In these cases, this extra burden can lead to fetal heart failure (hydrops). This situation can be dangerous for the fetus and mother.

SCTs occur in approximately 1 in every 35,000 live births and are more common in females than in males.

What will happen during pregnancy?

Approximately 60% of all SCTs are diagnosed by ultrasound prior to birth. In some cases, the tumor is so small that it goes undetected until delivery. If a SCT is detected, a targeted ultrasound will be performed to detect any associated abnormalities and a series of ultrasounds will be performed throughout pregnancy to monitor the size and growth of the SCT and to check for complications. A series of fetal echocardiograms (specialized ultrasounds of the fetal heart) may be recommended to closely monitor the fetal heart and check for early signs of heart failure.

Will a fetal treatment be required?

Almost all cases of SCT do not require fetal treatment. Most pregnancies will continue with only close monitoring. However, if the SCT grows to be very large or if the fetus shows signs of heart failure, fetal intervention to remove the tumor may be necessary. If this situation develops, your doctors at the Center will develop a comprehensive plan for you and your infant.

What special considerations should be made for delivery?

Type of delivery - A cesarean delivery may be recommended for large SCTs. A delivery plan will be carefully developed by your team of physicians at the Center and will be discussed with you and your obstetrician.

Place of delivery - The baby should be delivered at a hospital that is well prepared to handle the intensive care and surgery required of infants with an SCT. There should be a neonatal intensive care unit with the capability to provide specialized care and pediatric surgery services.

Time of delivery - Unless intervention is necessary because of fetal heart failure, there is usually no reason to intentionally induce early delivery. Large SCTs have been linked to preterm labor, and your physicians at the Center will discuss this possibility with you.

What will happen at birth?

Immediately following delivery, doctors will carefully evaluate your baby. In most cases, there is no immediate danger to the infant. Parents and family should be able to see and hold the newborn before transfer to the neonatal intensive care unit. The baby will be stabilized in a neonatal intensive care unit and your pediatric surgeon will evaluate the baby. Occasionally, the newborn may need help with breathing and blood pressure.

What will happen after delivery?

Once the baby has stabilized for a period of time, special x-rays may be required to determine the full extent of the SCT. Although it may seem like most of the tumor has grown on the outside of the baby, a portion of the SCT can grow internally. Surgery will be performed to remove the SCT. The complexity and risks associated with the surgery depend on the size and location of the tumor. Smaller, external tumors are easier to remove than larger tumors. Depending on the surgical outcomes, the baby may need to stay in the hospital for days or possibly weeks before going home.

What are the long-term outcomes and considerations?

The long-term prognosis of babies born with an SCT is excellent and most will go on to live normal lives. Most tumors are benign and only require careful monitoring after removal. It is important to monitor the child for signs that another tumor is developing, as recurrence is fairly common in the first few years of life. Some SCT’s may be cancerous. If this occurs, additional therapy may be required. Your pediatric surgeon will explain all of the aspects of SCT to you and your family.

Contact Us

Contact The Fetal Center to make an appointment with a high-risk pregnancy doctor.

Note: This information regarding your condition is meant to be a helpful, informative introduction. Because every newborn is different, this may not be applicable to all cases, especially if there are additional defects. Your team of experts at the Center will provide you with information specific to your pregnancy.