Krivchenia D Iu, Iurchenko N I, Almashiĭ G G, Iaremenko V V
Khirurgiia (Mosk). 1990 Aug(8):7-12.
Fifty children from one month to 14 years of age were examined and subjected to surgical treatment. Atresia of the bile ducts was diagnosed in 34 of them, hypoplasia of the bile ducts in 5, and a cyst of the choledochus in 11. Biliary atresia was managed by different variants of portoenterostomy, mostly after Kasai I, and two operations of cholecystojejunostomy were conducted in the so-called correctable type of atresia. 5 patients with biliary hypoplasia were treated by cholecystectomy, lavage of the bile ducts, and denervation of the hepatic artery. The following operations were carried out on 11 patients with a cyst of the choledochus: extirpation of the cyst with subsequent hepaticojejunostomy in 4, cystojejunostomy in 5, and cystoduodenostomy in 2 patients. Ultrasonic examination of the liver was undertaken in all 50 patients with impaired patency of the biliary tract as a screening test. Nine patients died in the postoperative period.
对50名年龄从1个月至14岁的儿童进行了检查并实施了手术治疗。其中34例被诊断为胆管闭锁,5例为胆管发育不全,11例为胆总管囊肿。胆管闭锁大多采用不同术式的肝门空肠吻合术,主要是在Kasai I术后进行,对于所谓可矫正型闭锁实施了2例胆囊空肠吻合术。5例胆管发育不全患者接受了胆囊切除术、胆管冲洗及肝动脉去神经支配术。对11例胆总管囊肿患者实施了以下手术:4例行囊肿切除并随后行肝管空肠吻合术,5例行囊肿空肠吻合术,2例行囊肿十二指肠吻合术。对所有50例胆道通畅受损的患者均进行了肝脏超声检查作为筛查。9例患者在术后死亡。