Clinical Experience of Currarino Syndrome.
- Author:
Taehoon KIM
1
;
Min Jeong CHO
;
Dae Yeon KIM
;
Seong Chul KIM
;
In Koo KIM
Author Information
1. Division of Pediatric Surgery, Asan Medical Center Children's Hospital, University of Ulsan Collage of Medicine, Seoul, Korea. sckim@amc.seoul.kr
- Publication Type:Original Article
- Keywords:
Currarino syndrome;
Anorectal malformation;
Constipation
- MeSH:
Anal Canal;
Anus, Imperforate;
Colostomy;
Constipation;
Dermoid Cyst;
Diagnosis, Differential;
Digestive System Abnormalities;
Dilatation;
Hirschsprung Disease;
Humans;
Lost to Follow-Up;
Meconium;
Meningomyelocele;
Parturition;
Rectum;
Reoperation;
Retrospective Studies;
Sacrum;
Spinal Cord;
Syringomyelia;
Teratoma
- From:Journal of the Korean Association of Pediatric Surgeons
2011;17(1):65-71
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Currarino syndrome is a hereditary syndrome characterized by the triad of a sacral bony defect, presacral mass and anorectal malformation. We retrospectively reviewed 13 Currarino syndrome patients who were treated in our center between 1997 and 2010. Demographic data, initial symptoms, initial diagnosis, pathologic diagnosis of presacral mass, associated anomalies and managements were analyzed. There were 8 boys and 5 girls. Four patients were diagnosed as Currarino syndrome immediately after birth with failure of passage of meconium and abdominal distension. Four patients underwent surgery for imperforate anus immediately after birth and were diagnosed as Currarino syndrome later and underwent reoperation. Three patients were diagnosed during work-up and management with of the tentative diagnosis of Hirschsprung's disease. Diagnosis of the remaining two patients was at the age of 26 months and 9 years and anorectal malformation was not associated. Twelve patients showed hemi-sacrum and one patient showed bilateral sacral subtotal agenesis. Two patients without anorectal malformation underwent presacral mass excision, untethering of spinal cord and repair of myelomeningocele. Six out of 8 patients, excluding 3 that expired or were lost to follow up, with anorectal malformation underwent colostomy, presacral mass excision, untethering of spinal cord, repair of myelomeningocele, posterior sagittal anorectoplasty and colostomy repair. One patient underwent only posterior sagittal anorectoplasty after colostomy. One waits the scheduled operation only with Hegar dilatation. Pathologic examation of presacral masses showed myelomeningoceles in 4 patients, lipomyelomeningoceles in 3 patients and dermoid cyst in one patient. Teratoma was combined in 2 patients. Eight patients needed neurosurgical operation for spinal cord problems. Seven patients had urologic anomalies and two of them underwent operation. Currarino syndrome should be considered as a differential diagnosis in pediatric patients with abdominal distension, constipation and anorectal malformation. For proper evaluation and treatment, a multi-disciplinary approach is recommended.
