epidural angiolipoma
Epidural angiolipomas are rare benign tumors composed of mature adipocytes and abnormal vessels.
Epidemiology
Epidural angiolipomas are more frequently encountered in women, and typically in middle age (40-50 years of age) .
Clinical presentation
In keeping with the slow growth of these tumors, clinical presentation is usually gradual with symptoms often present over a number of months/years. Signs and symptoms include:
- paraparesis
- back pain
- sensory changes (lower limbs)
- hyper-reflexia (lower limbs)
Radiographic features
Angiolipomas can be divided into infiltrating and non-infiltrating varieties, and both as seen in the epidural space. Non-infiltrating angiolipomas are more common and are usually located in the dorsal epidural space, typically in the thoracic region . Infiltrating angiolipomas are more common in the anterior epidural space, and can infiltrate not only adjacent soft tissues, but also adjacent vertebrae .
CT
CT demonstrates a mixture of soft tissue density and fatty components.
MRI
Signal characteristics are as expected from the composition of this tumor:
- T1
- high signal fatty component
- intermediate signal vascular component
- T2
- high signal
- flow voids are usually absent but enlarged vessels in the region may be visible
- T1 C+ (Gd)
- vivid enhancement of non-fatty components
Treatment and prognosis
Surgical resection is the treatment of choice, particularly for non-infiltrating tumors, in which case complete resection is possible and curative .
Malignant transformation has not been reported .
Differential diagnosis
Differential diagnosis includes other epidural masses :
- epidural metastases/lymphoma/multiple myeloma
- epidural lipomatosis
- Hirayama disease
- spinal meningioma