Sharma Satendra, Rashid Kumar Abdul, Dube Ravi, Malik G K, Tandon R K
Department of Pediatric Surgery, King George's Medical University, Lucknow, India.
J Indian Assoc Pediatr Surg. 2008 Apr;13(2):77-8. doi: 10.4103/0971-9261.43029.
This report is to present and discuss an extremely rare association of situs inversus with duodenal atresia in an 11-day-old male neonate born full term and weighing 1.9 kg. The baby presented with recurrent bilious vomiting. Babygram revealed situs inversus and duodenal obstruction. Echocardiography showed dextrocardia with a small ASD. Exploration confirmed a duodenal diaphragm with a central perforation between the third and fourth part of the duodenum and situs inversus. The literature search revealed 20 cases reported so far.
本报告旨在呈现并讨论一名11日龄足月出生、体重1.9千克的男性新生儿中,罕见的内脏反位与十二指肠闭锁的关联。该婴儿出现反复胆汁性呕吐。腹部平片显示内脏反位和十二指肠梗阻。超声心动图显示右位心伴小型房间隔缺损。手术探查证实为十二指肠隔膜,在十二指肠第三和第四部分之间有中央穿孔以及内脏反位。文献检索显示,迄今为止已报告20例。