Left hemihepatectomy for Schnelldorfer type C polycystic liver disease: A case report
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摘要:
<正>多囊肝(polycystic liver disease,PLD)是一类罕见的基因病,既可作为常染色体显性PLD单独存在,也可伴随常显或常隐多囊肾[1]。PLD的主要特点是胆管上皮细胞的过度生长,表现为肝实质多个弥散分布的囊性病变,常与成人多囊肾伴发。该病早期常无典型的症状及体征,肝功能正常,但中晚期随着肝体积的增大可出现腹胀、腹痛及腹部包块,影响患者的正常生活[2]。目前的治疗方式主要分为内科药物治疗和外科手术
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Key words:
- polycystic liver disease /
- polycystic kidney diseases /
- hepatectomy
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