Gao Pengfei, Liu Longshan, Zhang Zhichong, Xu Lingling, Wu Chenglin, Fu Qian, Li Jun, Wang Changxi
Organ Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Department of Pediatric Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Transl Pediatr. 2023 Feb 28;12(2):280-286. doi: 10.21037/tp-22-257. Epub 2023 Feb 14.
Intussusception is a frequent abdominal emergency in the pediatric population when the proximal bowel invaginates into the distal bowel. However, catheter-induced intussusception has not previously been described in pediatric renal transplant recipients, and the risk factors need to be investigated.
We report 2 cases of post-transplant intussusception which were caused by abdominal catheters. Case 1 experienced ileocolonic intussusception 3 months after renal transplantation and presented with intermittent abdominal pain; the intussusception was successfully managed using air enema. However, this child experienced a total of 3 episodes of intussusception within 4 days, which discontinued only after removal of the peritoneal dialysis catheter. No further intussusception recurrence was observed and the patient's intermittent pain disappeared during the follow-up. Case 2 developed ileocolonic intussusception 2 days after renal transplantation and presented currant jelly stools. The intussusception was completely irreducible until the intraperitoneal drainage catheter was eliminated; the patient discharged normal feces during the following days. A search in the databases of PubMed, Web of Science, and Embase yielded 8 similar cases. Our 2 cases had a younger age at disease onset than those retrieved in the search, and abdominal catheter was revealed as a lead point. Possible leading points of the 8 previously reported cases included post-transplant lymphoproliferative disorder (PTLD), acute appendicitis, tuberculosis, lymphocele, and firm adhesions. We noted that our cases were managed successfully with nonoperative treatment, whereas the 8 reported cases underwent surgical intervention. All of the 10 cases of intussusception occurred after renal transplantation and showed that intussusception had been induced by a lead point.
Our 2 cases implied that abdominal catheter could be a lead point to induce intussusception, especially in pediatric recipients with abdominal disorder. This experience may be applicable to other surgeries involving indwelling abdominal catheters in children. Health practitioners should consider this pathologic lead point and avoid serious consequences when intussusception occurs.
肠套叠是儿科常见的腹部急症,即近端肠管套入远端肠管。然而,此前尚未有关于儿科肾移植受者导管诱发肠套叠的报道,其危险因素有待研究。
我们报告2例由腹部导管引起的移植后肠套叠病例。病例1在肾移植后3个月发生回结肠套叠,表现为间歇性腹痛;经空气灌肠成功处理了肠套叠。然而,该患儿在4天内共发生3次肠套叠,仅在拔除腹膜透析导管后才停止。随访期间未观察到肠套叠复发,患者的间歇性疼痛消失。病例2在肾移植后2天发生回结肠套叠,出现果酱样大便。直到拔除腹腔引流导管,肠套叠才完全无法复位;随后几天患者排出正常粪便。在PubMed、科学网和Embase数据库中检索到8例类似病例。我们的2例病例发病年龄比检索到的病例小,且腹部导管被发现是诱因。此前报道的8例病例的可能诱因包括移植后淋巴增生性疾病(PTLD)、急性阑尾炎、结核病、淋巴囊肿和牢固粘连。我们注意到我们的病例通过非手术治疗成功治愈,而报道的8例病例均接受了手术干预。所有10例肠套叠均发生在肾移植后,表明肠套叠是由一个诱因引起的。
我们的2例病例表明,腹部导管可能是诱发肠套叠的诱因,尤其是在患有腹部疾病的儿科受者中。这一经验可能适用于其他涉及儿童留置腹部导管的手术。医护人员应考虑到这种病理诱因,在发生肠套叠时避免严重后果。