Expertise and Experience in Rare
Conditions
Cholesterol
granuloma is a rare inflammatory lesion that develops in the central skull base
and causes progressive thinning of surrounding bone and other nearby
structures. The lesion typically forms when blood from bone marrow leaks into a
nearby air cell. The trapped blood eventually breaks down and generates
significant inflammation, resulting in a buildup of fluid in the air cell. This
fluid-filled lesion slowly expands over time.
Specialists
at UT Southwestern are experts in applying the latest in image guidance and
microsurgical techniques to treat cholesterol granulomas while preserving quality
of life for each patient.
Symptoms
Some
cholesterol granulomas produce no symptoms. Symptoms of cholesterol granulomas
are caused by compression of nearby nerves and erosion of surrounding
structures, such as the inner ear or auditory canal. Those symptoms can include:
- Dizziness
- Double vision
- Facial numbness or pain
- Facial twitching or weakness
- Hearing loss
Diagnosis
Cholesterol
granulomas can be difficult to diagnose because they resemble other types of
lesions. At UT Southwestern, physicians perform a series of tests to make an
accurate diagnosis, such as:
Treatment for Cholesterol Granulomas
For
cholesterol granulomas with no symptoms, treatment might not be required. Instead,
physicians will monitor the lesion with serial MRI or CT scans.
For symptomatic
cholesterol granulomas, our physicians will drain the lesion. The drainage can
be done via endoscope, either through the nose or ear, depending on a patient’s
anatomy. If the lesion can’t be adequately drained using this minimally
invasive technique, surgical excision of the lesion might be required.
Clinical Trials and Research
Patients with
rare or complex skull base disorders such as cholesterol granuloma also benefit
from the leading research conducted at UT Southwestern, which often includes
clinical trials offered at few other centers in the country and helps speed
better treatment to patients.