Intestinal atresia and necrotizing enterocolitis: Embryology and anatomy |
| |
Affiliation: | 1. Translational Medicine Program, The Hospital for Sick Children, Toronto;2. Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto;1. Lead Pediatric Nurse Practitioner, Physical Medicine and Rehabilitation; Director, Traumatic Brain Injury/Concussion Clinic Dell Children''s Medical Center, Austin, TX, United States;2. Pediatric Surgery – UAMS Surgeon-in-Chief Rachel Fuller Endowed Chair Associate Trauma Medical Director Arkansas Children''s Hospital, United States;1. Nemours Children''s Healthcare, 807 Children''s Way, Jacksonville, FL 32207, United States;2. Wolfson Children''s Hospital, 800 Prudential Drive, Jacksonville, FL 32207, United States |
| |
Abstract: | The primitive gut originates at week 3 of gestation from the endoderm, with posterior incorporation of the remaining embryo layers. Wnt, Notch and TLR4 pathways have been shown to play central roles in the correct development of the intestine. The classical hypothesis for intestinal atresia development consists of failure in bowel recanalization or a vascular accident with secondary bowel reabsorption. These have been challenged due to the high frequency of associated malformations, and furthermore, with the discovery of molecular pathways and genes involved in bowel formation and correlated defects producing atresia.Necrotizing enterocolitis (NEC) has a multifactorial pathogenesis with prematurity being the most important risk factor; therefore, bowel immaturity plays a central role in NEC. Some of the same molecular pathways involved in gut maturation have been found to correlate with the predisposition of the immature bowel to develop the pathological findings seen in NEC. |
| |
Keywords: | |
本文献已被 ScienceDirect 等数据库收录! |
|