A series of 25 adult patients surgically treated for a tethered cord s
yndrome is reported. Preoperatively 19 patients presented with a senso
rimotor deficit in their lower limbs, 17 with sphincter disturbances,
12 with pain and/or neuroorthopedic symptoms and 9 with cutaneous lumb
ar anomalies. At surgery, an isolated anomaly (lipoma, anomalous or ad
herent Filum terminale) was disclosed in 18 patients. In the remaining
7, a more complex form of dysraphism was disclosed. Follow-up ranges
from 3 months to 20 years (mean : 6,5 years). Ten patients improved, 6
were stabilized and 9 showed continuous worsening. The best results w
ere obtained in patients in whom the cord tethering resulted from an a
nomalous filum terminale. Results were significantly worse in patients
suffering long standing symptomatology and showing either radiologica
lly or surgically mixed mechanisms of cord tethering. Early surgical c
orrection should be idealy undertaken in patients suffering from minor
neurological deficits and in whom magnetic resonance imaging illustra
tes a low conus medullaris attached by a short thickened filum termina
le.