Verma Shraddha, Bawa Monika, Rao Katragadda Lakshmi Narasimha, Sodhi Kushaljit Singh
Department of Pediatric Surgery, PGIMER, Chandigarh, India.
BMJ Case Rep. 2013 May 22;2013:bcr2012008056. doi: 10.1136/bcr-2012-008056.
Cystic caecal duplication is a rare congenital anomaly. We report a case of an infant, who presented with bilious vomiting and abdominal distension. On ultrasonography, intussusception with a cyst as a lead point was present in the right iliac fossa. On exploration, there was no evidence of intussusception, only caecal duplication cyst was found. To date, only three cases of caecal duplication which mimicked intussusception have been reported in the English literature.
盲肠重复囊肿是一种罕见的先天性异常。我们报告一例婴儿病例，该婴儿表现为胆汁性呕吐和腹胀。超声检查显示，右髂窝存在以囊肿为引导点的肠套叠。手术探查时，未发现肠套叠迹象，仅发现盲肠重复囊肿。迄今为止，英文文献中仅报道过3例类似肠套叠的盲肠重复囊肿病例。
