z-logo
open-access-imgOpen Access
Clinical and Histological Features of Different Types of Budd-Chiari Syndrome: A Comparison of 4 Cases
Author(s) -
Naoshi Nishida,
Shinichi Iwamura,
Hiroshi Ida,
Satoshi Hagiwara,
Yoshinori Kagioka,
Yasunori Minami,
Yoji Maetani,
Kyo Itoh,
Masatoshi Kudo
Publication year - 2013
Publication title -
digestive diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.879
H-Index - 66
eISSN - 1421-9875
pISSN - 0257-2753
DOI - 10.1159/000355237
Subject(s) - budd–chiari syndrome , medicine , inferior vena cava , cirrhosis , hepatic veins , hepatic veno occlusive disease , radiology , indocyanine green , vein , hepatic fibrosis , gastroenterology , pathology , disease , hematopoietic stem cell transplantation
Budd-Chiari syndrome (BCS) is a rare condition characterized by hepatic venous outflow obstruction. In this report, we present 4 cases of BCS with complete and incomplete obstruction of the inferior vena cava (IVC) and hepatic vein (HV). Each case showed different and unique features of liver damage, which were attributed to the site and degree of obstruction. Interestingly, improved liver functions such as increased serum albumin levels, decreased hyaluronic acid levels and a normal indocyanine green clearance test were evident within 1 month of the balloon angioplasty. Pericellular fibrosis and hypervascular regenerative nodules were also reversible after obstruction removal. Therefore, it is very important to manage this rare disease before it progresses to liver cirrhosis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom