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[Currarino triad : a case report].

作者信息

Miyake S, Kamikawa S, Kojima N, Yamamoto K, Kobayashi N, Yamazato M, Higashimoto Y, Tsugawa C, Kanegawa K, Tamaki N

机构信息

Department of Neurosurgery, Kobe Children's Hospital, Japan.

出版信息

No Shinkei Geka. 1996 Feb;24(2):189-93.

PMID:8849481
Abstract

The authors report a case of Currarino triad comprising anorectal malformations, sacral bony anomaly and presacral mass. A 1-year-old boy was presented with constipation as his chief complaint. No neurological deficit was found on admission. There was no cutaneous evidence of underlying spinal dysraphism. Lumbar X-ray films showed bony defect caudal to the third sacral vertebra. A barium-enema examination revealed an anterior displacement of the rectum. A myelography showed a presacral cavity filled with contrast medium. MRI demonstrated a thick filum terminale, and a round hypointense mass in the pelvis on T1 weighted images and hyperintense on T2 weighted images. Surgically we released the thick filum terminale, and obliterated the anterior sacral meningocele, because total removal would have been hazardous. Postoperatively transient dysuria was observed for a month, and the difficulty in defecation persisted. Recognition of this rare condition will lead to correct diagnosis and proper treatment.

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