Rogers Michael, Sylvester Francisco, Lichtman Steven
Department of Pediatric Gastroenterology, University of North Carolina Children's Hospital, Chapel Hill, NC.
ACG Case Rep J. 2018 Dec 5;5:e89. doi: 10.14309/crj.2018.89. eCollection 2018.
Congenital defects of bile acid synthesis are rare disorders that cause progressive liver dysfunction. Prolonged neonatal hyperinsulism (PNH) is a separate entity that leads to persistent hypoglycemia secondary to stress. We present a 4-month-old infant who presented with liver failure secondary to a bile acid synthesis defect. The patient's liver failure resolved with oral cholic acid therapy. This patient also developed PNH, which slowly resolved over time. This case illustrates a possible relationship between cholestatic liver failure and PNH. This relationship may help define specific stressors that increase the likelihood of developing PNH.
先天性胆汁酸合成缺陷是一种罕见的疾病,可导致进行性肝功能障碍。持续性新生儿高胰岛素血症(PNH)是一种独立的疾病,可导致因应激继发的持续性低血糖。我们报告一名4个月大的婴儿,因胆汁酸合成缺陷继发肝功能衰竭。口服胆酸治疗后,患者的肝功能衰竭得到缓解。该患者还出现了PNH,随着时间的推移逐渐缓慢缓解。该病例说明了胆汁淤积性肝功能衰竭与PNH之间可能存在的关系。这种关系可能有助于确定增加发生PNH可能性的特定应激源。