Literature DB >> 810946

Cholangiodysplastic pseudocirrhosis: light and electron microscopic examination.

M Balázs, V F Lukács, J Dénes, G Gorácz.   

Abstract

The familial type of cholangiodysplastic pseudocirrhosis is presented. This chronic liver disease is caused by malformation of the intrahepatic bile ducts. The female infant was 5 months old when the diagnosis was established. The liver biopsy was studied by light and electron microscopy. Electron microscopic examination revealed active proliferation of ductual cells and progression of fibrogenesis, findings consistent with the rapid and fatal course of the disease. In the case presented an acute cholangitis occurred, but after healing the progression of the original process led to hepatic insufficiency. It is suggested that cholangiodysplastic pseudocirrhosis is a chronic, progressive liver disease the course of which might be hastened by the complication of cholangitis; the process itself causes liver cirrhosis without inflammation.

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Year:  1975        PMID: 810946     DOI: 10.1007/BF00432167

Source DB:  PubMed          Journal:  Virchows Arch A Pathol Anat Histol        ISSN: 0340-1227


  23 in total

1.  [ON THE FAMILIAL PRESENCE OF INTRAHEPATIC BILE DUCT PROLIFERATIONS (CHOLANGIODYSPLASTIC PSEUDOCIRRHOSIS OF THE LIVER].

Authors:  H ALTHOFF
Journal:  Zentralbl Allg Pathol       Date:  1964-01-22

2.  [Simultaneous liver cirrhosis and cystic kidney in childhood].

Authors:  B WOHLGEMUTH; H MUHL
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1963

3.  Congenital hepatic fibrosis.

Authors:  D N KERR; C V HARRISON; S SHERLOCK; R M WALKER
Journal:  Q J Med       Date:  1961-01

Review 4.  Special article: functional implications of human portal and bile ductular ultrastructure.

Authors:  I Sternlieb
Journal:  Gastroenterology       Date:  1972-08       Impact factor: 22.682

Review 5.  Mechanisms and control of secretion of bile water and electrolytes.

Authors:  S Erlinger; D Dhumeaux
Journal:  Gastroenterology       Date:  1974-02       Impact factor: 22.682

6.  [The clinical picture of inspissated bile syndrome].

Authors:  V F Lukács; M Balázs; J Dénes
Journal:  Acta Paediatr Acad Sci Hung       Date:  1972

7.  Three-dimensional reconstruction of intrahepatic bile ducts in a case of polycystic disease of the liver in an infant.

Authors:  M Jorgensen
Journal:  Acta Pathol Microbiol Scand A       Date:  1972

8.  Biliary secretion in a patient with cystic dilation of the intrahepatic biliary tree.

Authors:  L A Turnberg; E A Jones; S Sherlock
Journal:  Gastroenterology       Date:  1968-06       Impact factor: 22.682

9.  Congenital malformations of the intrahepatic biliary tree in the adult.

Authors:  W T Foulk
Journal:  Gastroenterology       Date:  1970-02       Impact factor: 22.682

10.  Fibrogenesis in congenital hepatic fibrosis. An electron and light microscopic study.

Authors:  J Albukerk; J L Duffy
Journal:  Arch Pathol       Date:  1971-08
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