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Intestinal malrotation with concurrent duodenal duplication cyst in a 1-day-old infant
- Source :
- Journal of Pediatric Surgery Case Reports, Vol 85, Iss , Pp 102422- (2022)
- Publication Year :
- 2022
- Publisher :
- Elsevier, 2022.
-
Abstract
- Congenital intestinal malrotation and duodenal duplication cysts are congenital anomalies that are present during the neonatal period. The presence of both in a single patient is exceedingly rare with limited similar case reports present in the literature. We present the case of a neonate diagnosed with a right-sided ovarian cyst in utero, who was later found to have a concurrent duodenal duplication cyst and intestinal malrotation. Treatment consisted of open Ladd's procedure, resection of duplication cyst, and primary duodenoduodenostomy. The report serves as a data point for this rare phenomenon as well as provides surgical options for similar cases.
Details
- Language :
- English
- ISSN :
- 22135766
- Volume :
- 85
- Issue :
- 102422-
- Database :
- Directory of Open Access Journals
- Journal :
- Journal of Pediatric Surgery Case Reports
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.1e6e64ec85a45d78ad7d91fc21b457f
- Document Type :
- article
- Full Text :
- https://doi.org/10.1016/j.epsc.2022.102422