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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2501| Title: | Currarino triad with a duplicate anal canal presenting with an infected sacral mass | Authors: | Wong, M. Lee, S. W. Kimble, R. M. Lumsden, E. Kendrick, D. J. |
Issue Date: | 2022 | Source: | 78 , 2022 | Journal: | Journal of Pediatric Surgery Case Reports | Abstract: | Currarino syndrome is a rare congenital malformation characterised by the triad of: an anorectal malformation, sacral bony defect and presacral mass. One rare but possible anorectal malformation is an anal canal duplication, a congenital anomaly which is not only the most distal but also the rarest form of digestive tract duplication. We present the case of a four-year-old female who had a complete form of the Currarino triad including an anal canal duplication.L20165619352022-01-28 | DOI: | 10.1016/j.epsc.2022.102185 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L2016561935&from=exporthttp://dx.doi.org/10.1016/j.epsc.2022.102185 | | Keywords: | bacterium culture;Bacteroides fragilis;bone defect;case report;child;clinical article;constipation;currarino syndrome;female;fever;human;image reconstruction;laminectomy;leukocyte count;anorectal malformation;meningomyelocele;nuclear magnetic resonance imaging;preschool child;sacrum;spinal dysraphism;Staphylococcus aureus;vomiting;x-ray computed tomography;anal canal duplication;anal canal;C reactive proteinabdominal pain;lumbosacral spine;anorexia;apparent diffusion coefficient;article;autosomal dominant disorder | Type: | Article |
| Appears in Sites: | Children's Health Queensland Publications |
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