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Evaluation of a new histologic staging and grading system for primary biliary cirrhosis in comparison with classical systems

Authors :
Yasuharu Kaizaki
Atsuhiro Kawashima
Yasuni Nakanuma
Hajime Ohta
Shuichi Terasaki
Eishiro Mizukoshi
Hirofumi Okafuji
Kenichi Harada
Motoko Sasaki
Yuko Kakuda
Shuichi Kaneko
Seiko Sawada-Kitamura
Hiroko Ikeda
Yasunori Sato
Satomi Kasashima
Source :
Human Pathology. 44:1107-1117
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

Recently, our research team proposed a new histologic staging and grading system for primary biliary cirrhosis (PBC) that takes into account necroinflammatory activity and histologic heterogeneity. The present study aimed to confirm the usefulness of the new evaluation system. A total of 152 liver biopsy specimens and clinical data (including outcomes in patients with PBC before treatment with ursodeoxycholic acid) were analyzed with respect to the new system. Staging was evaluated on the basis of 3 histologic components (fibrosis, bile duct loss, and deposition of orcein-positive granules), and grading was assessed on the basis of chronic cholangitis activity and hepatitis activity. Concurrently, the classical systems, that is, the Scheuer and Ludwig staging systems, were also assessed and compared with our new system. PBC cases showed different distributions in each stage of the 3 systems. The new staging and grading system reflected liver dysfunctions before specific treatment. This was on a par with the results obtained using the classical systems. Development of cirrhosis-related conditions correlated well with the new staging system compared with the 2 classical staging systems, and in particular, the amount of deposition of orcein-positive granules could reflect development of cirrhosis-related conditions (scores 0-1 versus scores 2-3 groups, P < .0001). In conclusion, the new PBC staging system was demonstrated to reflect clinicolaboratory features, and its progression was associated with the development of cirrhosis-related conditions. © 2013 Elsevier Inc. All rights reserved.

Details

ISSN :
00468177
Volume :
44
Database :
OpenAIRE
Journal :
Human Pathology
Accession number :
edsair.doi.dedup.....5c0b4d90c9fcf65791b0cd660f5642ac
Full Text :
https://doi.org/10.1016/j.humpath.2012.09.017