Sarkar Shruti, Apte Ashwin, Sarkar Nupur, Sarkar Dipankar, Longia Sheela
Department of Pediatrics, Peoples College of Medical Science & Research Center, Bhopal, India.
BMJ Case Rep. 2011 Apr 1;2011:bcr0120113779. doi: 10.1136/bcr.01.2011.3779.
Congenital duodenal anomalies like atresia, stenosis and web or diaphragm commonly present in the neonatal age with signs of intestinal obstruction. Duodenal webs can sometimes present in early infancy and very rarely beyond infancy. The authors present a case of congenital duodenal web with a very small central aperture in a 2-year-old child with presenting features of persistent vomiting and resultant failure to thrive without any overt signs of intestinal obstruction.
先天性十二指肠异常，如闭锁、狭窄以及蹼或隔膜，通常在新生儿期出现肠梗阻症状。十二指肠蹼有时可在婴儿早期出现，极少在婴儿期之后出现。作者报告了一例2岁儿童先天性十二指肠蹼的病例，其中心孔径非常小，表现为持续呕吐，进而生长发育不良，且无任何明显的肠梗阻迹象。
