Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney Disease

被引：24

作者：

Wen, Jessica ^{[1
,2
]}

机构：

[1] Childrens Hosp Philadelphia, Div Gastroenterol Hepatol & Nutr, Philadelphia, PA 19104 USA

[2] Univ Penn, Sch Med, Dept Pediat, Philadelphia, PA 19104 USA

来源：

CTS-CLINICAL AND TRANSLATIONAL SCIENCE | 2011年 / 4卷 / 06期

关键词：

liver disease; pediatrics; cirrhosis; RENIN-ANGIOTENSIN SYSTEM; TISSUE GROWTH-FACTOR; CLINICAL-EXPERIENCE; BILIARY DYSGENESIS; INTRACELLULAR CA2+; MAMMALIAN TARGET; EPITHELIAL-CELLS; LIVER FIBROSIS; DETECT CHANGES; PRIMARY CILIUM;

D O I：

10.1111/j.1752-8062.2011.00306.x

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

Autosomal recessive polycystic kidney disease (ARPKD) is a developmental disorder that mainly affects the kidneys and the biliary tract. Affected patients often have massively enlarged cystic kidneys as well as congenital hepatic fibrosis (CHF) characterized by dilated bile ducts and associated peribiliary fibrosis. This review will examine what is known about ARPKD-associated liver disease and will highlight areas of ongoing research into its pathogenesis and potential treatment. Clin Trans Sci 2011; Volume 4: 460465

引用

页码：460 / 465

页数：6

共 50 条

[21] Effect of calcium-sensing receptor activation in models of autosomal recessive or dominant polycystic kidney disease [J].

Wang, Xiaofang ;

Harris, Peter C. ;

Somlo, Stefan ;

Batlle, Daniel ;

Torres, Vicente E. .

NEPHROLOGY DIALYSIS TRANSPLANTATION, 2009, 24 (02) :526-534

[22] Molecular and cellular pathogenesis of autosomal dominant polycystic kidney disease [J].

Bastos, A. P. ;

Onuchic, L. F. .

BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2011, 44 (07) :606-617

[23] Comparative proteomic analysis suggests that mitochondria are involved in autosomal recessive polycystic kidney disease [J].

Li, Qing-Wei ;

Lu, Xiao-Yan ;

You, Yong ;

Sun, Huan ;

Liu, Xin-Yu ;

Ai, Jian-Zhong ;

Tan, Rui-Zhi ;

Chen, Tie-Lin ;

Chen, Mian-Zhi ;

Wang, Hong-Lian ;

Wei, Yu-Quan ;

Zhou, Qin .

PROTEOMICS, 2012, 12 (15-16) :2556-2570

[24] Autosomal recessive polycystic kidney disease: The prototype of the hepato-renal fibrocystic diseases [J].

Guay-Woodford, Lisa M. .

JOURNAL OF PEDIATRIC GENETICS, 2014, 3 (02) :89-101

[25] Complications and prognosis of patients diagnosed with autosomal recessive polycystic kidney disease in neonatal period [J].

Inoki, Yuta ;

Nishi, Kentaro ;

Osaka, Kei ;

Kaneda, Tomoya ;

Akiyama, Misaki ;

Sato, Mai ;

Ogura, Masao ;

Ide, Kentaro ;

Kamei, Koichi .

CEN CASE REPORTS, 2024, 13 (03) :181-187

[26] Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease [J].

Denamur, Erick ;

Delezoide, Anne-Lise ;

Alberti, Corinne ;

Bourillon, Agnes ;

Gubler, Marie-Claire ;

Bouvier, Raymonde ;

Pascaud, Olivier ;

Elion, Jacques ;

Grandchamp, Bernard ;

Michel-Calemard, Laurence ;

Missy, Pascale ;

Zaccaria, Isabelle ;

Le Nagard, Herve ;

Gerard, Benedicte ;

Loirat, Chantal .

KIDNEY INTERNATIONAL, 2010, 77 (04) :350-358

[27] New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications [J].

Telega, Grzegorz ;

Cronin, David ;

Avner, Ellis D. .

PEDIATRIC TRANSPLANTATION, 2013, 17 (04) :328-335

[28] Individualized concept for the treatment of autosomal recessive polycystic kidney disease with end-stage renal disease [J].

Miura, Kenichiro ;

Sato, Yasuyuki ;

Yabuuchi, Tomoo ;

Kaneko, Naoto ;

Ishizuka, Kiyonobu ;

Chikamoto, Hiroko ;

Akioka, Yuko ;

Nawashiro, Yuri ;

Hisano, Masataka ;

Imamura, Hideaki ;

Miyai, Takayuki ;

Sakamoto, Seisuke ;

Kasahara, Mureo ;

Fuchinoue, Shohei ;

Okumi, Masayoshi ;

Ishida, Hideki ;

Tanabe, Kazunari ;

Hattori, Motoshi .

PEDIATRIC TRANSPLANTATION, 2020, 24 (03)

[29] Liver Disease in Autosomal Recessive Polycystic Kidney Disease: Clinical Characteristics and Management in Relation to Renal Failure [J].

Luoto, Topi T. ;

Pakarinen, Mikko P. ;

Jahnukainen, Timo ;

Jalanko, Hannu .

JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2014, 59 (02) :190-196

[30] Autosomal dominant polycystic kidney disease [J].

Cornec-Le Gall, Emilie ;

Alam, Ahsan ;

Perrone, Ronald D. .

LANCET, 2019, 393 (10174) :919-935

← 1 2 3 4 5 →