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胆汁酸合成缺陷与高胰岛素血症

Bile Acid Synthesis Defect and Hyperinsulinism.

作者信息

Rogers Michael, Sylvester Francisco, Lichtman Steven

机构信息

Department of Pediatric Gastroenterology, University of North Carolina Children's Hospital, Chapel Hill, NC.

出版信息

ACG Case Rep J. 2018 Dec 5;5:e89. doi: 10.14309/crj.2018.89. eCollection 2018.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a44c/6358580/7287820ff754/CG-CGCR180077F001.jpg

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