Department of Pediatric Surgery, Shengjing Hospital, China Medical University, Shenyang, PR China.
J Pediatr Surg. 2010 Mar;45(3):627-9. doi: 10.1016/j.jpedsurg.2009.12.025.
Tubular rectal duplication is a very rare congenital anomaly. We report a case of tubular rectal duplication in a newborn baby who presented with perianal sepsis. The diagnosis was confirmed by barium enema, magnetic resonance imaging, and at operation. We performed total mucosectomy through a posterior sagittal incision combined with laparotomy. The patient was doing quite well at 17-month follow-up examination.
管状直肠重复畸形是一种非常罕见的先天性异常。我们报告了一例新生儿管状直肠重复畸形病例,该患儿表现为肛周脓肿。诊断通过钡灌肠、磁共振成像和手术得到证实。我们通过后路纵切联合剖腹手术进行了全直肠黏膜切除术。患者在 17 个月的随访检查中恢复良好。