Innovative Techniques for Optimal Treatment
Chordomas are rare malignant tumors that develop from the cellular remnants of the notochord, an embryologic structure in the head. These tumors occur most commonly in middle-aged patients.
Approximately one-third of chordomas arise at the skull base in a region called the clivus – a critical location in the center of the skull bordering major blood vessels, optic nerves, and the brainstem.
Specialists at UT Southwestern take a team approach to treating chordomas, applying the latest in image guidance and microsurgical techniques to preserve quality of life for each patient.
Symptoms of Chordomas
Chordomas are slow-growing tumors. As they grow, they put pressure on nearby areas of the brain and spinal cord, causing symptoms such as:
- Facial numbness
- Severe headaches
- Vision changes
Diagnosis
UT Southwestern physicians diagnose chordomas using imaging studies, such as:
- Computed tomography (CT) scans can show a mass at the central skull base with surrounding bony destruction.
- Magnetic resonance imaging (MRI) can help the physician understand the tumor’s relationship to the adjacent structures.
Treatments for Chordoma
Surgical removal of these tumors is the main treatment strategy. These surgeries can be challenging, given the aggressive nature of chordomas and their proximity to vital structures.
UT Southwestern physicians work together to determine the best approach for each patient. Minimally invasive endoscopic approaches are used whenever possible to optimize success rates and minimize complications and recovery time. In some cases, radiotherapy is also recommended.
Research and Clinical Trials
Patients also benefit from the leading research conducted at UT Southwestern, which often includes clinical trials offered at few other centers in the country and which helps speed better treatment to patients.