Sanchez Sabrina, Javid Patrick, Ricca Robert, Avansino Jeffrey
Department of Surgery, University of Washington, Seattle, WA, USA.
Pediatr Transplant. 2012 Sep;16(6):E225-8. doi: 10.1111/j.1399-3046.2011.01569.x. Epub 2011 Aug 23.
A rare case of a colocolonic intussusception in a pediatric cardiac transplant patient is reported along with a review of colocolonic intussusception in pediatric patients after organ transplantation. A four-yr-old girl with a history of heart transplantation shortly after birth presented with a 12-hour history of abdominal pain, vomiting, and bloody stools. Initial abdominal x-ray showed rectal edema. A rectal examination revealed a palpable intussusceptum that prompted a therapeutic contrast enema, which failed to reduce the intussusception. Surgical exploration was performed with reduction of the intussusception and resection of the terminal ileum and cecum. A pathologic lead point was not identified.
本文报告了一例小儿心脏移植患者发生结肠-结肠套叠的罕见病例,并对器官移植后小儿患者的结肠-结肠套叠进行了综述。一名4岁女童,出生后不久即有心脏移植史,出现腹痛、呕吐和血便12小时。最初的腹部X线检查显示直肠水肿。直肠检查发现可触及套叠肠管,遂行治疗性造影灌肠,但套叠未能复位。进行了手术探查,复位套叠并切除末端回肠和盲肠。未发现病理性套叠起始点。