Alagille D
J Hepatol. 1985;1(5):561-5. doi: 10.1016/s0168-8278(85)80753-4.
Two types of paucity of interlobular bile ducts (PIBD) may be observed in children with chronic cholestasis. The syndromatic type (80 cases) is the most frequent. The non-syndromatic type (32 cases) is the most severe and half of the patients in this group died from liver failure in the first years of life. The main therapeutic point is that patients with PIBD should not be operated on. The only treatment available is symptomatic medical treatment: the main helpful possibilities concern feeding of medium-chain triglycerides, large supplementation of liposoluble vitamins (A, D, E and K) given intramuscularly, phenobarbital and cholestyramine when there is severe pruritus. The place of the liver transplantation will be clarified in the near future.
在患有慢性胆汁淤积症的儿童中,可观察到两种类型的小叶间胆管缺乏(PIBD)。综合征型(80例)最为常见。非综合征型(32例)最为严重,该组中有一半患者在生命的头几年死于肝功能衰竭。主要的治疗要点是,患有PIBD的患者不应接受手术治疗。唯一可用的治疗方法是对症药物治疗:主要的有益措施包括给予中链甘油三酯饮食、大量肌肉注射脂溶性维生素(A、D、E和K)、在出现严重瘙痒时使用苯巴比妥和消胆胺。肝移植的地位将在不久的将来得以明确。