Split cord malformations (SCMs) may occur in conjunction with myelomeningoc
eles, and are often ignored or misdiagnosed, potentially causing spinal cor
d tethering. In this paper, we study the incidence and clinical significanc
e of such an association. We have retrospectively reviewed the medical reco
rds and radiographs of 20 myelomeningocele patients who had a SCM. These co
mprised at least 6% of our myelomeningocele patients. Five of the 20 had si
multaneous repair of both lesions at birth. The other 15 were diagnosed wit
h the SCM in a delayed fashion (mean age 4.4 years). Clinical presentations
that prompted a diagnostic investigation included hypertrichosis (1), pain
(2), routine radiographic follow-up (2), neurourological deterioration (10
) and progressive scoliosis (5). In 17 of the 20 patients, the SCM involved
the placode or was within one level of it. Fifteen of these were in the ar
ea of the placode or one segment above it. Five of the 20 patients had hype
rtrichosis and 15 of the 20 patients had a bony midline septum (i.e. type I
SCM). Several accompanying spinal dysraphic lesions also contributed to th
e tethering: thickened (previously inconspicuous) filum terminale (6), syri
ngohydromyelia (5) and a neurenteric cyst with a benign teratoma (1). Arach
noiditis secondary to the prior myelomeningocele repair was found, as expec
ted, in all 15 patients. However, in virtually all patients, there was also
evidence of tethering at the level of the SCM. Long-term follow-up showed
stabilization of preoperative symptoms and signs, whereas complications of
the operation and clinical evidence of retethering were uncommon. Myelomeni
ngocele patients should be screened with clinical examinations looking for
hypertrichosis and with spinal radiographs preoperatively looking for evide
nce of SCM (bony midline septum and/or interpedicular widening not due to t
he myelomeningocele). Intraoperatively, the placode and the rostral spinal
cord segment should be carefully inspected for an SCM and other dysraphic l
esions.