Cserni Tamás, Magyar Agnes, Németh Tamás, Paran Thambipillai Sri, Csízy István, Józsa Tamas
Department of Pediatric Surgery, Medical and Health Science Center, University of Debrecen, Nagyerdei krt. 98, 4012 Debrecen, Hungary.
Surg Today. 2006;36(12):1126-8. doi: 10.1007/s00595-006-3302-x. Epub 2006 Dec 25.
Intestinal atresia involving the ileocecal region is a very rare intestinal malformation, and the presence or absence of the ileocecal valve influences its surgical management. We report the case of a male newborn with a provisional diagnosis of distal ileal atresia, in whom laparotomy revealed that the entire ileocecal region was atretic with an absent ileocecal valve and appendix vermiformis. We resected the dilated terminal ileum together with the atretic segment and performed an ileocolic anastomosis between the terminal ileum and the transverse microcolon without valve reconstruction. When last seen, 8 months after the operation, the baby was developing normally. Ileocolic anastomosis without valve replacement appears to be sufficient if an ileocecal valve is completely absent and only a short segment of the terminal ileum is lost.
累及回盲部的肠闭锁是一种非常罕见的肠道畸形,回盲瓣的有无会影响其手术治疗。我们报告一例初步诊断为回肠远端闭锁的男性新生儿病例,剖腹探查发现整个回盲部闭锁,回盲瓣和阑尾缺如。我们切除了扩张的回肠末端连同闭锁段,并在回肠末端与无瓣膜重建的横结肠微型结肠之间进行了回结肠吻合术。在术后8个月最后一次随访时,患儿发育正常。如果回盲瓣完全缺如且仅丢失一小段回肠末端,不进行瓣膜置换的回结肠吻合术似乎就足够了。