PRIMARY TUMORS OF THE SPINE IN CHILDREN - NATURAL-HISTORY, MANAGEMENT, AND LONG-TERM FOLLOW-UP

Citation
Sj. Beer et Ah. Menezes, PRIMARY TUMORS OF THE SPINE IN CHILDREN - NATURAL-HISTORY, MANAGEMENT, AND LONG-TERM FOLLOW-UP, Spine (Philadelphia, Pa. 1976), 22(6), 1997, pp. 649-658
Citations number
47
Categorie Soggetti
Orthopedics,"Clinical Neurology
ISSN journal
03622436
Volume
22
Issue
6
Year of publication
1997
Pages
649 - 658
Database
ISI
SICI code
0362-2436(1997)22:6<649:PTOTSI>2.0.ZU;2-M
Abstract
Study Design. Patients 16 years of age and younger with primary verteb ral neoplasms diagnosed between 1951 and 1996 at The University of Iow a were reviewed retrospectively with specific consideration given to f ollow-up. Objective. Follow-up extending beyond the growth of the axia l skeleton was used to establish the natural history, management, outc ome, and current approach to treatment. Summary of Background Data. Pr imary tumors of the spine are uncommon. The treatment of such lesions generally has been based on small series of tumors, or extrapolated fr om the treatment of tumors in other regions and tumors in adults. Give n the unique developing anatomy and dynamic nature of the growing spin e in children, delineating appropriate modalities or treatment for the se tumors beyond the growth of the axial skeleton is essential. Method s. Clinical history, radiographs, radiographic reports, and interviews were used to establish this database. Outcome with respect to the var ious approaches to treatment was then compared in detail. Results. For ty-five patients were identified in which follow-up greater than 10 ye ars was available for 58% of patients. There were 29 histologically be nign and 16 malignant tumors. Patients presented most frequently with pain (79%) and neurologic deficits (74%). The duration of symptoms was significantly shorter with malignant tumors (11 weeks) compared with benign tumors (26 weeks). Radiographic abnormalities were demonstrated on plain radiographs in 98% of cases. Tumor excision was achieved in 80%. Follow-up studies were available beyond the growth of the axial s keleton in these patients, with an average follow-up of 14 years. Recu rrence was seen in 6 of 45 children, and the overall mortality rate wa s 6.7%, occurring only with malignant tumors. Conclusion. Our current approach to treatment of spinal neoplasms varies from that used in the earlier part of the series and reflects the need for single stage com plete resection and stabilization.