Pd. Sawin et al., SYMPTOMATIC INTRASELLAR HEMANGIOBLASTOMA IN A CHILD TREATED WITH SUBTOTAL RESECTION AND ADJUVANT RADIOSURGERY - CASE-REPORT, Journal of neurosurgery, 84(6), 1996, pp. 1046-1050
The first documented case of a symptomatic intrasellar hemangioblastom
a is described, occurring in an 11-year-old girl with stigmata of von
Hippel-Lindau disease who presented with headaches, progressive bitemp
oral hemianopsia, and adenohypophysial dysfunction. A subtotal resecti
on of the lesion was achieved with two separate surgical procedures: a
transsphenoidal approach and a subfrontal craniotomy. Subsequent grow
th of residual tumor was treated with combined conventional radiothera
py and stereotactic radiosurgery. Two years following completion of th
ese adjuvant therapies, no residual tumor was evident on magnetic reso
nance imaging. Previous experience with hemangioblastoma in this regio
n, as well as the rationale for radiotherapy in the treatment of incom
pletely resected lesions, is reviewed.