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Front Pediatr. 2017 Jun 7;5:114. doi: 10.3389/fped.2017.00114. eCollection 2017.
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Hepatoblastoma in molecularly defined, congenital diseases.分子定义的先天性疾病中的肝母细胞瘤。
Am J Med Genet A. 2022 Sep;188(9):2527-2535. doi: 10.1002/ajmg.a.62767. Epub 2022 Apr 28.
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Remodeling of Intrahepatic Ducts in a Model of Caroli Syndrome: Is Scar Carcinoma a Consequence of Laplace's Law?卡洛里综合征模型中肝内胆管的重塑：瘢痕癌是拉普拉斯定律的结果吗？
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1
Malignant tumors of the liver in children.儿童肝脏恶性肿瘤
Semin Pediatr Surg. 2016 Oct;25(5):265-275. doi: 10.1053/j.sempedsurg.2016.09.002. Epub 2016 Sep 4.
2
Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease.在捷克常染色体隐性多囊肾病家庭中通过新一代测序对PKHD1进行分子遗传学分析。
BMC Med Genet. 2015 Dec 22;16:116. doi: 10.1186/s12881-015-0261-3.
3
Glomerulocystic Kidney Disease and Hepatoblastoma in an Infant: A Rare Presentation.婴儿期肾小球囊性肾病合并肝母细胞瘤：一种罕见的表现。
Case Rep Nephrol Dial. 2015 Nov 14;5(3):200-3. doi: 10.1159/000439520. eCollection 2015 Sep-Dec.
4
The Children's Hepatic tumors International Collaboration (CHIC): Novel global rare tumor database yields new prognostic factors in hepatoblastoma and becomes a research model.儿童肝肿瘤国际协作组（CHIC）：新型全球罕见肿瘤数据库揭示了肝母细胞瘤新的预后因素并成为一种研究模式。
Eur J Cancer. 2016 Jan;52:92-101. doi: 10.1016/j.ejca.2015.09.023. Epub 2015 Dec 1.
5
Novel variant syndrome associated with congenital hepatic fibrosis.与先天性肝纤维化相关的新型变异综合征。
World J Clin Cases. 2015 Oct 16;3(10):904-10. doi: 10.12998/wjcc.v3.i10.904.
6
Pure fetal histology subtype was associated with better prognosis of children with hepatoblastoma: A Chinese population-based study.纯胎儿组织学亚型与肝母细胞瘤患儿的更好预后相关：一项基于中国人群的研究。
J Gastroenterol Hepatol. 2016 Mar;31(3):621-7. doi: 10.1111/jgh.13165.
7
Impact of postoperative complications on overall survival of patients with hepatoblastoma.术后并发症对肝母细胞瘤患者总生存期的影响。
Pediatr Blood Cancer. 2015 Jan;62(1):24-8. doi: 10.1002/pbc.25240. Epub 2014 Sep 22.
8
Liver disease in autosomal recessive polycystic kidney disease: clinical characteristics and management in relation to renal failure.常染色体隐性多囊肾病中的肝脏疾病：与肾衰竭相关的临床特征及管理
J Pediatr Gastroenterol Nutr. 2014 Aug;59(2):190-6. doi: 10.1097/MPG.0000000000000422.
9
Genetics and epigenetics of hepatoblastoma.肝母细胞瘤的遗传学和表观遗传学。
Pediatr Blood Cancer. 2012 Nov;59(5):785-92. doi: 10.1002/pbc.24213. Epub 2012 Jul 13.
10
Prognostic stratification for children with hepatoblastoma: the SIOPEL experience.肝母细胞瘤患儿的预后分层：SIOPEL 经验。
Eur J Cancer. 2012 Jul;48(10):1543-9. doi: 10.1016/j.ejca.2011.12.011. Epub 2012 Jan 13.

1例伴有常染色体隐性多囊肾病和卡洛里综合征的肝母细胞瘤疑难病例——文献综述

A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome-Review of the Literature.

作者信息

Kadakia Nevil, Lobritto Steven J, Ovchinsky Nadia, Remotti Helen E, Yamashiro Darrell J, Emond Jean C, Martinez Mercedes

机构信息

Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY, United States.

Department of Pediatrics, Children's Hospital of Montefiore, Bronx, NY, United States.

出版信息

Front Pediatr. 2017 Jun 7;5:114. doi: 10.3389/fped.2017.00114. eCollection 2017.

DOI:10.3389/fped.2017.00114
PMID:28638817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5461266/
Abstract

We report a rare case of an 18-month-old female with autosomal recessive polycystic kidney disease, Caroli syndrome, and pure fetal type hepatoblastoma. The liver tumor was surgically resected with no chemotherapy given. Now 9 years post resection she demonstrates no local or distant recurrence and stable renal function.

摘要

我们报告了一例罕见病例，一名18个月大的女性患有常染色体隐性多囊肾病、卡罗里综合征和单纯胎儿型肝母细胞瘤。肝脏肿瘤通过手术切除，未进行化疗。现在切除术后9年，她没有出现局部或远处复发，肾功能稳定。