Department of Pediatric Metabolism and Nutrition, Dr. Sami Ulus Child Health and Diseases & Maternity Hospital, Ankara, Turkey.
Indian J Pediatr. 2013 Jun;80(6):502-4. doi: 10.1007/s12098-012-0842-5. Epub 2012 Jul 15.
Neonatal cholestasis is a rare presenting feature of cystic fibrosis which usually cannot be differentiated from other types of cholestasis. Herein, the authors report a 63 d-old boy with cystic fibrosis presenting with neonatal cholestasis mimicking biliary atresia. A new mutation in CFTR gene resulting in severe phenotype has been described. The cystic fibrosis patients with c.3871 G > T mutation may have acholic gaita mimicking biliary atresia in the absence of insipissated bile with minimal histologic findings in the liver.
新生儿胆汁淤积症是囊性纤维化的一种罕见表现,通常无法与其他类型的胆汁淤积症区分。本文报道了一例囊性纤维化患儿,以新生儿胆汁淤积症为表现,类似于胆道闭锁。该患儿 CFTR 基因突变导致严重表型。囊性纤维化患者 c.3871 G>T 突变可能会出现无浓稠胆汁的无胆绿素性灰白色粪便,肝脏组织学表现轻微,类似于胆道闭锁。