E. Tasdemiroglu et Ra. Patchell, NEUROLOGIC COMPLICATIONS OF THE PRIMARY PEDIATRIC EXTRACRANIAL NEUROBLASTOMAS, Neurological research, 19(1), 1997, pp. 45-50
Between January 1982 and June 1994, 32 children with primary extracran
ial neuroblastomas (n=24) and ganglioneuroblastomas (n=8) were admitte
d and treated at the UKMC. Twenty-two (68.7%) of these patients suffer
ed with 29 neurological complications (up to 3 complications per case)
during the course of their disease. Fourteen cases had nervous system
metastases or invasion. Nonmetastatic complications, such as nervous
system infections (n=4) and new onset of seizures secondary to brain m
etastasis, hypertensive and metabolic encephalopathies (n=3) were seen
on 7 cases. Five cases had treatment related complications, one case
first presented with opsoclonus-polymyoclonus syndrome. Eight of these
22 patients died, due to relapse or progression of the disease. The m
ean follow-up period of 14 surviving patients was 44.9 months (range,
12-110 months). Five of these 14 patients suffered with neurologic seq
uelae. The incidence of neurologic complications was 68.7%. Nervous sy
stem metastasis was the most common neurologic complication. Although
5 patients suffered with neurologic sequelae, outcome was not influenc
ed by presence of neurologic complication.