Denève E, Maillet O, Blanc P, Fabre J-M, Nocca D
Service de chirurgie digestive II, hôpital Saint-Eloi, CHU de Montpellier, avenue Bertin-Sans, 34295 Montpellier, France.
J Gynecol Obstet Biol Reprod (Paris). 2008 Dec;37(8):796-8. doi: 10.1016/j.jgyn.2008.06.006. Epub 2008 Jul 23.
We report the case of a 43-year-old woman, who presented a complete and non-reductible ileo-cecal intussusception with pre-occlusion. An ileocecal resection with ileocolic anastomosis was performed. The pathologic examination confirmed the diagnosis of colic endometriosis with transmural lesions, causing the intussusception. Altough the digestive endometriosis is quite classical and well-known, particulary with vermiform appendix and rectosigmoïd involvement, ileo-cecal intussusception secondary to endometriosis is rare.
我们报告了一例43岁女性患者，其出现了完全性且不可复位的伴有梗阻前状态的回盲部肠套叠。进行了回盲部切除术并做了回结肠吻合术。病理检查确诊为结肠子宫内膜异位症伴透壁性病变，导致了肠套叠。尽管消化道子宫内膜异位症较为常见且广为人知，尤其是累及阑尾和直肠乙状结肠时，但子宫内膜异位症继发回盲部肠套叠却很罕见。
