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Caroli's disease and autosomal dominant polycystic kidney disease: a rare association?

作者信息

Mousson C, Rabec M, Cercueil J P, Virot J S, Hillon P, Rifle G

机构信息

Department of Nephrology-Intensive Care, Centre Hospitalier Universitaire, Dijon, France.

出版信息

Nephrol Dial Transplant. 1997 Jul;12(7):1481-3. doi: 10.1093/ndt/12.7.1481.

DOI:10.1093/ndt/12.7.1481
PMID:9249792
Abstract
摘要

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Caroli's disease and autosomal dominant polycystic kidney disease: a rare association?卡罗里病与常染色体显性多囊肾病：一种罕见的关联？
Nephrol Dial Transplant. 1997 Jul;12(7):1481-3. doi: 10.1093/ndt/12.7.1481.
2
Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease.一名常染色体显性多囊肾病（ADPKD）合并卡罗里病患者的复发性胆管炎
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Caroli's syndrome and adult polycystic kidney disease.卡罗里氏综合征与成人多囊肾病。
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Congenital hypothyroidism in association with Caroli's disease and autosomal recessive polycystic kidney disease: patient report.先天性甲状腺功能减退症合并卡罗里病和常染色体隐性多囊肾病：病例报告
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[Caroli disease in a kidney transplant patient with polycystic kidney disease].[一名患有多囊肾病的肾移植患者的卡罗里病]
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Pregnancy complicated by Caroli's disease with polycystic kidney disease: a case report and following observations.妊娠合并卡罗里病伴多囊肾病：一例报告及随访观察
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Caroli's syndrome with autosomal recessive polycystic kidney disease in a two month old infant.一名两个月大婴儿患卡罗利综合征合并常染色体隐性多囊肾病。
Yonsei Med J. 2006 Feb 28;47(1):131-4. doi: 10.3349/ymj.2006.47.1.131.
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[Caroli's disease, congenital hepatic fibrosis and renal polycystosis: a little frequent association].
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Autosomal recessive polycystic kidney disease.常染色体隐性多囊肾病
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Pathogenesis of Choledochal Cyst: Insights from Genomics and Transcriptomics.先天性胆总管囊肿的发病机制：从基因组学和转录组学角度的新见解。
Genes (Basel). 2022 Jun 8;13(6):1030. doi: 10.3390/genes13061030.
2
Hepatointestinal complications in polycystic kidney disease.多囊肾病的肝肠并发症
Oncotarget. 2017 Sep 15;8(46):80971-80980. doi: 10.18632/oncotarget.20901. eCollection 2017 Oct 6.
3
Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease.一名常染色体显性多囊肾病（ADPKD）合并卡罗里病患者的复发性胆管炎
Intern Med. 2016;55(20):3009-3012. doi: 10.2169/internalmedicine.55.6818. Epub 2016 Oct 15.
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Caroli's disease: Description of a case with a benign clinical course.卡罗里病：一例临床病程良性的病例描述。
Ann Gastroenterol. 2011;24(2):129-133.
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Whole exome sequencing identifies recessive PKHD1 mutations in a Chinese twin family with Caroli disease.全外显子组测序在一个患卡罗利病的中国双胞胎家庭中鉴定出隐性PKHD1突变。
PLoS One. 2014 Apr 7;9(4):e92661. doi: 10.1371/journal.pone.0092661. eCollection 2014.
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Caroli's syndrome in a post renal transplant patient: case report and review of the literature.肾移植后患者的 Caroli 综合征：病例报告及文献复习。
Saudi J Gastroenterol. 2012 Jan-Feb;18(1):59-61. doi: 10.4103/1319-3767.91728.
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Nephrectomy in patients with Caroli's and ADPKD may be associated with increased morbidity.对于患有卡罗里病和常染色体显性多囊肾病的患者，肾切除术可能会增加发病率。
Can Urol Assoc J. 2011 Apr;5(2):E19-22. doi: 10.5489/cuaj.10054.
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Choledochal cysts: part 1 of 3: classification and pathogenesis.胆总管囊肿：3部分系列之第1部分：分类与发病机制
Can J Surg. 2009 Oct;52(5):434-40.
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Choledochal cysts: analysis of disease pattern and optimal treatment in adult and paediatric patients.胆总管囊肿：成人和儿童患者的疾病模式分析和最佳治疗方法。
HPB (Oxford). 2007;9(5):383-7. doi: 10.1080/13651820701646198.
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Caroli's disease: identification and treatment strategy.卡罗里病：识别与治疗策略
Curr Gastroenterol Rep. 2007 Apr;9(2):151-5. doi: 10.1007/s11894-007-0010-7.