Spinal abnormalities in classic bladder exstrophy

Objective  To determine the frequency and clinical sequelae of significant spinal malformations in children born with classic bladder exstrophy. Patients and methods  All patients evaluated or treated for classic bladder exstrophy at this institution were reviewed retrospectively. Radiographs or rep...

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Published in:British Journal of Urology Vol. 79; no. 6; pp. 975 - 978
Main Authors: CADEDDU, J.A., BENSON, J.E., SILVER, R.I., LAKSHMANAN, Y., JEFFS, R.D., GEARHART, J.P.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Science Ltd 01-06-1997
Blackwell
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Summary:Objective  To determine the frequency and clinical sequelae of significant spinal malformations in children born with classic bladder exstrophy. Patients and methods  All patients evaluated or treated for classic bladder exstrophy at this institution were reviewed retrospectively. Radiographs or reports pertinent to the spine were retrieved and reviewed with a paediatric radiologist and all vertebral abnormalities categorized. Clinical charts of those with spinal anomalies were reviewed to determine any clinical neurological disorders associated with the radiographic findings. Results  Of 423 patients with classic bladder exstrophy who were identified, 299 had radiographs or reports available for adequate review. Of these, 34 (11%) normal variants, e.g. spina bifida occulta and lumbarization or sacralization of vertebrae, were identified. Abnormalities of spinal curvature were identified in eight patients (2.7%), all with uncomplicated scoliosis. Spinal dysraphism was diagnosed in 12 patients (4%) and included myelomeningocele, lipomeningocele, scimitar sacrum, posterior laminal defects in two or more vertebrae, vertebral fusion and hemivertebrae. The one patient with myelomeningocele had clinical neurological dysfunction, giving an overall incidence of 0.3%. Conclusions  Spinal anomalies, excluding normal variants, occur in children born with classic bladder exstrophy at a rate of about 6.7%. The incidence of this association is much less than that for cloacal exstrophy. Although rare, neurological dysfunction can occur in the case of spinal dysraphism. Paediatric urologists and neurologists should be aware of this significant difference between patients with classic bladder and cloacal exstrophy to properly diagnose, evaluate and treat the attendant neurological problems.
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ISSN:0007-1331
1464-410X
DOI:10.1046/j.1464-410X.1997.00190.x