Late Diagnosis of Complete Colonic and Rectal Duplication in a Girl with an Anorectal Malformation

• DOI: 10.1055/s-0039-1692193
• Publication Date: 2019-07-05T19:43:17Z
• Authors: Amr AbdelHamid Ab...; Shaimaa Abdelsatt...; Sherif Elhussiny ...; Anas Fagelnor; Ahmad Zaki
• Keywords: Cloaca; Anus

Abstract Complete colonic duplication is rare, and usually occurs as a part of the caudal syndrome. In such cases, diagnosis clinically evident by presence two ani arranged side in perineum, which commonly associated with external genitalia well (double phallus or double vestibule). this report, we present special case anorectal anomaly that was complete tubular duplication. The initially missed due to uncommon sagittal arrangement duplicated rectum: one rectum ending externally into perineum rectoperineal fistula, while other hidden its internal termination vagina. Our final for variant female, One colon (which free mesenteric border) terminated anteriorly vagina “short common channel” cloaca, fistula. Although seems be rather complex confusing, yet our an excellent outcome benign type anomalies (rectoperineal fistula cloaca) absence significant sacral dysplasia; addition adequate identification abnormal anatomy appropriate investigations staged approach surgical reconstruction.