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[Wolman's disease in an infant].
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本文引用的文献

1
Diagnosis and treatment of congenital tuberculosis: a systematic review of 92 cases.先天性结核病的诊断与治疗:92 例病例的系统回顾
Orphanet J Rare Dis. 2019 Jun 10;14(1):131. doi: 10.1186/s13023-019-1101-x.
2
Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents.一对患病父母所生孩子的先天性脂肪代谢障碍综合征的临床与遗传学特征
BMC Med Genet. 2018 May 29;19(1):88. doi: 10.1186/s12881-018-0610-0.
3
Lysosomal acid lipase deficiency allograft recurrence and liver failure- clinical outcomes of 18 liver transplantation patients.溶酶体酸性脂肪酶缺乏症肝移植复发和肝功能衰竭-18 例肝移植患者的临床结局。
Mol Genet Metab. 2018 May;124(1):11-19. doi: 10.1016/j.ymgme.2018.03.010. Epub 2018 Mar 27.
4
Wolman's disease and cholesteryl ester storage disorder: the phenotypic spectrum of lysosomal acid lipase deficiency.沃尔曼病和胆固醇酯贮积症:溶酶体酸性脂肪酶缺乏的表型谱。
Lancet Gastroenterol Hepatol. 2017 Sep;2(9):670-679. doi: 10.1016/S2468-1253(17)30052-3.
5
Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study.接受sebelipase Alfa治疗的溶酶体酸性脂肪酶缺乏症婴儿的生存情况:一项开放标签、多中心、剂量递增研究。
Orphanet J Rare Dis. 2017 Feb 8;12(1):25. doi: 10.1186/s13023-017-0587-3.
6
A rare constellation of imaging findings in Wolman disease.沃尔曼病中罕见的一系列影像学表现。
Med J Armed Forces India. 2015 Dec;71(Suppl 2):S448-51. doi: 10.1016/j.mjafi.2014.02.006. Epub 2014 Apr 26.
7
Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infants.婴儿期溶酶体酸性脂肪酶缺乏症的快速进展与死亡率
Genet Med. 2016 May;18(5):452-8. doi: 10.1038/gim.2015.108. Epub 2015 Aug 27.
8
Extended use of a selective inhibitor of acid lipase for the diagnosis of Wolman disease and cholesteryl ester storage disease.酸性脂肪酶选择性抑制剂的延长使用在沃曼病和胆固醇酯贮积症的诊断中的应用。
Gene. 2014 Apr 10;539(1):154-6. doi: 10.1016/j.gene.2014.02.003. Epub 2014 Feb 6.
9
Primary familial xanthomatosis with involvement and calcification of the adrenals. Report of two more cases in siblings of a previously described infant.原发性家族性黄瘤病伴肾上腺受累及钙化。此前报道的一名婴儿的同胞中又有两例病例报告。
Pediatrics. 1961 Nov;28:742-57.
10
Niemann-Pick disease type C: diagnosis and outcome in children, with particular reference to liver disease.C型尼曼-匹克病:儿童的诊断与预后,尤其涉及肝脏疾病
J Pediatr. 1993 Aug;123(2):242-7. doi: 10.1016/s0022-3476(05)81695-6.

沃尔曼病:婴儿胆汁淤积和肝硬化的罕见病因。

Wolman's Disease: A Rare Cause of Infantile Cholestasis and Cirrhosis.

作者信息

Menon Jagadeesh, Shanmugam Naresh, Srinivas Sripriya, Vij Mukul, Jalan Anil, Srinivas Reddy Mettu, Rela Mohamed

机构信息

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.

出版信息

J Pediatr Genet. 2020 Aug 20;11(2):132-134. doi: 10.1055/s-0040-1715119. eCollection 2022 Jun.

DOI:10.1055/s-0040-1715119
PMID:35769959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9236733/
Abstract

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.

摘要

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。