The natural history and management of symptomatic and asymptomatic vertebral hemangiomas

• Published in: Journal of neurosurgery Vol. 78; no. 1; pp. 36 - 45
• Main Authors: FOX, M. W, ONOFRIO, B. M
• Format: Journal Article
• Language: English
• Published: Park Ridge, IL American Association of Neurological Surgeons 1993
• Subjects: Adolescent; Adult; Aged; Biological and medical sciences; Child; Combined Modality Therapy; Diseases of the osteoarticular system; Diseases of the spine; Embolization, Therapeutic; Female; Hemangioma - complications; Hemangioma - diagnosis; Hemangioma - surgery; Hemangioma - therapy; Humans; Laminectomy; Magnetic Resonance Imaging; Male; Medical sciences; Middle Aged; Recurrence; Retrospective Studies; Spinal Cord Compression - etiology; Spinal Cord Compression - therapy; Spinal Neoplasms - complications; Spinal Neoplasms - diagnosis; Spinal Neoplasms - surgery; Spinal Neoplasms - therapy; Tomography, X-Ray Computed; Human; Compression; Disease of the spine; Nervous system diseases; Spine; Diseases of the osteoarticular system; Cardiovascular disease; Asymptomatic; Retrospective; Vascular disease; Angioma; Treatment; Complication; Evolution; Spinal cord disease
• ISSN: 0022-3085; 1933-0693
• DOI: 10.3171/jns.1993.78.1.0036

Fifty-nine cases of vertebral hemangioma were seen at the Mayo Clinic between 1980 and 1990. Vertebral hemangiomas were discovered incidentally in 35 patients, while pain was the presenting complaint in 13 patients. Five patients presented directly with progressive neurological deficit requiring surgery, and six patients had surgery elsewhere for spinal cord compression and were referred for follow-up evaluation. To better define the natural history of these lesions, a historical review of these patients was conducted; progression of an asymptomatic or painful lesion to neurological symptoms was found in only two cases (mean follow-up period 7.4 years, range 1 to 35 years). New-onset back pain followed by subacute progression (mean time to progression 4.4 months, range 0.25 to 12 months) of a thoracic myelopathy was the most common presentation for patients with neurological deficit. Initially, all 11 patients with spinal cord compression underwent decompressive surgery with full neurological recovery. Recurrent neurological symptoms were observed in three of six patients following subtotal tumor resection and postoperative administration of 1000 cGy or less radiation therapy (mean follow-up period 8.7 years, range 1 to 17 years). No recurrences were noted in four patients who had subtotal excision plus radiotherapy between 2600 and 4500 cGy. One other patient had gross total tumor removal without radiotherapy and has not had a recurrence. Based on these patients and a review of the literature, the authors recommend annual neurological and radiological examinations for patients with hemangiomas associated with pain, especially young females with thoracic lesions in whom spinal cord compression is most likely to develop. Radiation therapy or embolization is an effective therapeutic alternative for patients with severe medically refractory pain. Regular follow-up monitoring for patients with asymptomatic lesions is unnecessary unless pain develops at the appropriate spinal level. It is concluded that management of patients with a progressive neurological deficit should include preoperative angiography and embolization, decompressive surgery with the approach determined by the degree of vertebral involvement and site of spinal cord compression, and postoperative radiation therapy in patients following subtotal tumor removal. Operative management and complications are discussed.