Neuropathic Bladder Caused by Caudal Regression Syndrome without Any Other Neurogenic SymptomsReportar como inadecuado

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Case Reports in MedicineVolume 2012 2012, Article ID 982418, 3 pages

Case ReportDepartment of Nephro-Urology, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan

Received 7 July 2011; Accepted 30 April 2012

Academic Editor: Ron Rabinowitz

Copyright © 2012 Yoshinobu Moritoki et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Caudal regression syndrome CRS is a rare congenital vertebral anomaly, which occurs most often in combination with spinal cord malformations and morphologic dysfunctions of the lower extremities; these signs are useful for both patients and clinicians in the diagnosis of this syndrome. However, in certain cases, clinicians have failed to identify the syndrome due to the lack of apparent anomalies, resulting in the progression of renal dysfunction caused by neuropathic bladder when CRS is eventually identified. Here, we report a case of a 2-year-old girl who was referred to our hospital for vesicoureteral reflux. At examination, she presented no neurological symptoms; however, on cystourethrography and CT scanning we found that the sacral bone was absent, through which CRS was diagnosed. A urodynamic study indicated detrusor-sphincter dyssynergia, and clean intermittent catheterization was initiated. In the present report, we describe a case of CRS with no neurologic symptoms other than a neuropathic bladder. The lack of outward signs can result in delayed diagnosis. Thus, urological examinations, including a urodynamic study, might be the only clue for identifying an underlying neurologic injury involving the lower spinal cord.

Autor: Yoshinobu Moritoki, Yoshiyuki Kojima, Hideyuki Kamisawa, Kentaro Mizuno, Kenjiro Kohri, and Yutaro Hayashi



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