CONGENITAL HEPATIC FIBROSIS WITHOUT ANY SYMPTOMS AS DIAGNOSED BY LAPAROSCOPY

被引:3
作者
Kisaka, Yoshiyasu [1 ]
Abe, Masanori [1 ]
Tokumoto, Yoshio [1 ]
Hirooka, Masashi [1 ]
Shigematsu, Shuichiro [1 ]
Koizumi, Yohei [1 ]
Murakami, Hidehiro
Matsuura, Bunzo [1 ]
Hiasa, Yoichi [1 ]
Onji, Morikazu [1 ]
机构
[1] Ehime Univ, Grad Sch Med, Dept Gastroenterol & Metabol, Toon, Ehime 7910295, Japan
关键词
congenital hepatic fibrosis; elastography; laparoscopy; POLYCYSTIC KIDNEY-DISEASE;
D O I
10.1111/j.1443-1661.2010.01033.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The present report represents the case of a 36-year-old woman with congenital hepatic fibrosis (CHF). She was admitted to our hospital because of gastric varices. She was asymptomatic and her liver function tests were within normal limits. Computed tomography showed hepatomegaly, splenomegaly and collateral circulation, but no evidence of liver cirrhosis. Real-time tissue elastography suggested severe fibrosis of the liver. Laparoscopy showed wide and discrete white markings on the surface of the liver and she was diagnosed with CHF based on the histological examination. The findings obtained from elastography and laparoscopy were useful for making the diagnosis of CHF.
引用
收藏
页码:357 / 359
页数:3
相关论文
共 10 条
[1]   Performance of transient elastography for the staging of liver fibrosis: A meta-analysis [J].
Friedrich-Rust, Mireen ;
Ong, Mei-Fang ;
Martens, Swantje ;
Sarrazin, Christoph ;
Bojunga, Joerg ;
Zeuzem, Stefan ;
Herrmann, Eva .
GASTROENTEROLOGY, 2008, 134 (04) :960-974
[2]  
Kerkar Nanda, 2006, Clin Liver Dis, V10, P55, DOI 10.1016/j.cld.2005.10.003
[3]  
KERR DN, 1961, Q J MED, V30, P91
[4]  
MCCARTHY LJ, 1965, GASTROENTEROLOGY, V49, P27
[5]  
SHIOMI S, 1999, DIGEST ENDOSC, V11, P174
[6]  
Shizuma T, 2000, GASTROENTEROL ENDOSC, V42, P50
[7]   Experience of a single center with congenital hepatic fibrosis: A review of the literature [J].
Shorbagi, Ali ;
Bayraktar, Yusuf .
WORLD JOURNAL OF GASTROENTEROLOGY, 2010, 16 (06) :683-690
[8]   Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) [J].
Turkbey, Baris ;
Ocak, Iclal ;
Daryanani, Kailash ;
Font-Montgomery, Esperanza ;
Lukose, Linda ;
Bryant, Joy ;
Tuchman, Maya ;
Mohan, Parvathi ;
Heller, Theo ;
Gahl, William A. ;
Choyke, Peter L. ;
Gunay-Aygun, Meral .
PEDIATRIC RADIOLOGY, 2009, 39 (02) :100-111
[9]   The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein [J].
Ward, CJ ;
Hogan, MC ;
Rossetti, S ;
Walker, D ;
Sneddon, T ;
Wang, XF ;
Kubly, V ;
Cunningham, JM ;
Bacallao, R ;
Ishibashi, M ;
Milliner, DS ;
Torres, VE ;
Harris, PC .
NATURE GENETICS, 2002, 30 (03) :259-269
[10]   Is congenital hepatic fibrosis a pure liver disease? [J].
Yonem, Ozlem ;
Ozkayar, Nihal ;
Balkanci, Ferhun ;
Harmanci, Ozgur ;
Sokmensuer, Cenk ;
Ersoy, Osman ;
Bayraktar, Yusuf .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (06) :1253-1259