Department of Surgery, Washington University in St Louis, St Louis Children's Hospital, MO 63110, USA.
J Am Coll Surg. 2011 Jan;212(1):62-7. doi: 10.1016/j.jamcollsurg.2010.09.017. Epub 2010 Nov 30.
Intestinal obstruction is a rare but serious complication after liver transplantation. Adhesions are the most common cause of obstruction in the nontransplantation setting; however, after pediatric liver transplantation unusual causes must be considered.
A prospectively maintained institutional database was analyzed for all reoperations for intestinal obstruction on pediatric liver allograft recipients from 1990 to 2009.
During the study period, 181 pediatric patients underwent liver transplantation at the study center. The most common indication for transplantation was biliary atresia. Seven patients required reoperation for intestinal obstruction. All 7 patients had abdominal operations before transplantation and 5 of 7 received reduced-size grafts. No patients had adhesive small bowel obstruction. The cause was right-sided diaphragmatic hernia in 4 and post-transplantation lymphoproliferative disorder (PTLD) in 3. Diaphragmatic hernia was demonstrated by chest radiograph in 3 of 4 patients. The fourth was taken to surgery with a presumptive diagnosis of intestinal obstruction and a diaphragmatic hernia was found at exploration. In patients with PTLD causing obstruction, 2 presented with an obstructing mass and the third presented with intussusception. Mean time to reoperation was 29 months after liver transplantation. Patients with diaphragmatic hernia presented earlier post-transplantation than those with PTLD (4.2 ± 2.4 months versus 59.3 ± 54.6 months, respectively; p = 0.0003, Fisher's exact test). Six patients are alive at a median follow-up of 5.8 years. One patient succumbed to recurrent B-cell lymphoma.
Intestinal obstruction after pediatric liver transplantation is commonly related to what would conventionally be considered unusual causes. A high index of suspicion must be maintained and early operative therapy considered as obstruction because causes such as diaphragmatic hernia and PTLD are unlikely to resolve with conservative measures.
肠阻塞是肝移植后罕见但严重的并发症。在非移植环境中,粘连是最常见的梗阻原因;然而,在小儿肝移植后,必须考虑到不常见的原因。
分析了 1990 年至 2009 年期间,因肠阻塞而行再次手术的所有小儿肝移植受者的前瞻性维持机构数据库。
在研究期间,181 名小儿患者在研究中心接受了肝移植。移植的最常见指征是胆道闭锁。7 例患者需要因肠阻塞而再次手术。7 例患者在移植前均行腹部手术,其中 5 例行减体积移植。无患者发生粘连性小肠梗阻。4 例为右侧膈疝,3 例为移植后淋巴组织增生性疾病(PTLD)。膈疝在 3 例患者中通过胸部 X 线片显示。第 4 例患者因疑似肠梗阻而行手术,术中发现膈疝。因 PTLD 导致梗阻的患者中,2 例表现为梗阻性肿块,第 3 例表现为肠套叠。肝移植后再次手术的平均时间为 29 个月。膈疝组患者比 PTLD 组患者更早出现(分别为 4.2 ± 2.4 个月和 59.3 ± 54.6 个月;p = 0.0003,Fisher 确切概率法)。6 例患者在中位随访 5.8 年后仍存活。1 例患者死于复发性 B 细胞淋巴瘤。
小儿肝移植后肠阻塞通常与传统上认为不常见的原因有关。必须保持高度怀疑,并考虑早期手术治疗,因为膈疝和 PTLD 等原因不太可能通过保守治疗得到解决。