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.