Menon Jagadeesh, Shanmugam Naresh, Srinivas Sripriya, Vij Mukul, Jalan Anil, Srinivas Reddy Mettu, Rela Mohamed
Department of Pediatric Gastroenterology and Hepatology, Dr. Rela Institute & Medical Center, Bharat Institute of Higher Education and Research, Chennai, India.
Department of Radiology and Imaging, Dr. Rela Institute & Medical Center, Bharat Institute of Higher Education and Research, Chennai, India.
J Pediatr Genet. 2020 Aug 20;11(2):132-134. doi: 10.1055/s-0040-1715119. eCollection 2022 Jun.
Liver cirrhosis in infancy can be secondary to various etiologies such as biliary atresia, familial cholestatic and metabolic disorders. Wolman's disease (WD) is a lysosomal storage disorder caused by the absence of lysosomal acid lipase enzyme activity and a significant association with infantile cholestasis and cirrhosis. We encountered an infant presenting with advanced cirrhosis and decompensation having splenomegaly for which the underlying etiology was found to be WD and the diagnostic clue came from abdominal X-ray showing bilateral adrenal calcifications. The diagnosis was confirmed by genetic analysis. The outcome was poor and died before 6 months of age without enzyme replacement therapy or hematopoietic stem cell transplantation.
婴儿期肝硬化可能继发于多种病因,如胆道闭锁、家族性胆汁淤积和代谢紊乱。沃尔曼病(WD)是一种溶酶体贮积病,由溶酶体酸性脂肪酶活性缺乏引起,与婴儿胆汁淤积和肝硬化有显著关联。我们遇到一名患有晚期肝硬化和失代偿且脾肿大的婴儿,其潜在病因被发现是WD,诊断线索来自腹部X线显示双侧肾上腺钙化。通过基因分析确诊。由于没有酶替代疗法或造血干细胞移植,该婴儿预后不良,在6个月龄前死亡。