Grosfeld J L, Rescorla F J, Skinner M A, West K W, Scherer L R
Department of Surgery, Whitcomb Riley Hospital for Children, Indiana University School of Medicine, Indianapolis.
Arch Surg. 1994 May;129(5):513-8; discussion 518-20. doi: 10.1001/archsurg.1994.01420290059009.
To assess the results of surgical treatment of infants and children with biliary tract disease.
The records of children with biliary tract disorders requiring surgical intervention were reviewed retrospectively. Diagnosis, age, sex, clinical presentation, treatment, and outcome were evaluated.
A large pediatric referral facility.
A total of 300 patients treated from 1972 through 1993 were evaluated, including 102 with biliary atresia, 29 with choledochal cyst, and 169 with cholelithiasis. Hepatic portoenterostomy was performed in 87 patients with biliary atresia, and biopsy alone was performed in 15. Twenty girls and nine boys, 50% of whom were younger than 3 years, had choledochal cyst. Operative management included cyst excision and hepatojejunostomy in 25 patients, cyst jejunostomy in two patients, cystduodenostomy in one patient, and choledochocele excision in one patient. Gallstones were observed in 106 girls and 63 boys; 28 were aged 0 to 5 years, 31 were aged 6 to 10 years, and 110 were aged 11 to 18 years. Open cholecystectomy was performed in 143 patients, and laparoscopic cholecystectomy was performed in 26 patients.
Principal outcomes examined were surgical morbidity and mortality.
Hepatic portoenterostomy was successful in 28 (32%) of 87 patients with biliary atresia (all younger than 3 months), and 23 showed improvement following hepatic portoenterostomy; hepatic portoenterostomy failed in 36 patients. Twenty-eight (82.3%) of 34 patients survived liver transplantation. Overall survival was 71.5%. Survival of patients with choledochal cyst was 96.4% (28/29). Cholecystectomy was successful in all 169 patients. There were eight complications and one death (0.59% mortality).
Survival in patients with biliary atresia (71%) has improved with hepatic portoenterostomy complemented by liver transplantation. Hepatic portoenterostomy is the procedure of choice in infants younger than 3 months. An improved outlook for patients with choledochal cyst can be expected after cyst excision and hepatojejunostomy. Gallstones are relatively common in children. Both open and laparoscopic cholecystectomy are safe and effective procedures in children.
评估婴幼儿及儿童胆道疾病的手术治疗结果。
回顾性分析需要手术干预的胆道疾病患儿的病历。对诊断、年龄、性别、临床表现、治疗及预后进行评估。
一家大型儿科转诊机构。
对1972年至1993年期间接受治疗的300例患者进行评估,其中102例为胆道闭锁,29例为胆总管囊肿,169例为胆结石。87例胆道闭锁患者行肝门空肠吻合术,15例行单纯活检。20例女孩和9例男孩患有胆总管囊肿,其中50%年龄小于3岁。手术治疗包括25例行囊肿切除及肝空肠吻合术,2例行囊肿空肠吻合术,1例行囊肿十二指肠吻合术,1例行胆总管囊肿切除术。观察到106例女孩和63例男孩有胆结石;28例年龄在0至5岁,31例年龄在6至10岁,110例年龄在11至18岁。143例患者行开腹胆囊切除术,26例患者行腹腔镜胆囊切除术。
主要观察指标为手术并发症及死亡率。
87例胆道闭锁患者中,28例(32%)肝门空肠吻合术成功(均小于3个月),23例肝门空肠吻合术后病情改善;36例肝门空肠吻合术失败。34例患者中28例(82.3%)肝移植后存活。总体生存率为71.5%。胆总管囊肿患者生存率为96.4%(28/29)。169例患者胆囊切除术均成功。有8例并发症,1例死亡(死亡率0.59%)。
肝门空肠吻合术联合肝移植可提高胆道闭锁患者的生存率(71%)。肝门空肠吻合术是3个月以下婴儿的首选术式。囊肿切除及肝空肠吻合术后,胆总管囊肿患者的预后有望改善。胆结石在儿童中相对常见。开腹及腹腔镜胆囊切除术在儿童中均为安全有效的手术方式。