Feasibility of histological grading and staging of chronic viral hepatitis using specimens obtained by thin-needle biopsy

被引:34
作者
Petz, D
Klauck, S
Röhl, FW
Malfertheiner, P
Roessner, A
Röcken, C
机构
[1] Otto von Guericke Univ, Dept Pathol, D-39120 Magdeburg, Germany
[2] Otto von Guericke Univ, Dept Gastroenterol Hepatol & Infect Dis, Magdeburg, Germany
[3] Otto von Guericke Univ, Dept Biometr, Magdeburg, Germany
关键词
menghini; histopathology; liver biopsy;
D O I
10.1007/s00428-002-0749-z
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We performed a retrospective study to investigate the feasibility of grading and staging of chronic viral hepatitis on specimens obtained by means of thin-needle biopsy (TNB; 20G) using the modified Ishak-system (J Hepatol 1995; 22:696-699). Specimens obtained using large-needle biopsy (LNB; 17G) served as a control. A total of 100 biopsy specimens from 88 patients were included in the study. Of the patients, 30 suffered from chronic hepatitis B, 54 from chronic hepatitis C, and 4 from both; 59 specimens were obtained by TNB and 41 by LNB. All four categories of the Ishak-system, i.e., interface hepatitis, confluent necrosis, lobular inflammation and portal inflammation, could be applied to TNB specimens and provided similar total scores to those observed in LNB specimens. Specimens obtained by TNB facilitated the diagnosis of liver cirrhosis. However, they bore the risk of underestimating the presence of cirrhosis in favor of advanced bridging fibrosis, whereas no differences were found in the overall recognition of liver fibrosis. Intra- and interobserver variabilities were not affected by the needle size. For the interobserver agreement, the kappa values for the category of inflammation ranged from 0.003 to 0.419 (TNB) and 0.096 to 0.470 (LNB) and for staging we noted kappa values of 0.351 (TNB) and 0.456 (LNB). Reproducibility increased when a tolerance of 1 was accepted for grading (total score) and staging; in this case, observer variability was less than 20%. This study showed that grading and staging of chronic viral hepatitis is feasible in TNB specimens and that intra- and interobserver variability poses a greater problem than needle size.
引用
收藏
页码:238 / 244
页数:7
相关论文
共 28 条
[1]  
BEDOSSA P, 1994, HEPATOLOGY, V20, P15
[2]  
Bortz J., 1990, VERTEILUNGSFREIE MET, DOI 10.1007/978-3-662-22593-6
[3]   PATTERN OF NECROSIS IN ACUTE VIRAL HEPATITIS - PROGNOSTIC VALUE OF BRIDGING (SUBACUTE-HEPATIC-NECROSIS) [J].
BOYER, JL ;
KLATSKIN, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (20) :1063-+
[4]  
CHEVALLIER M, 1994, HEPATOLOGY, V20, P349, DOI 10.1002/hep.1840200213
[5]  
COOKSLEY WGE, 1986, HEPATOLOGY, V6, P345
[6]  
Di Bisceglie Adrian M., 1999, American Journal of Medicine, V107, p53S
[7]  
EDOUTE Y, 1992, AM J GASTROENTEROL, V87, P1138
[8]   Viral load and clinicopathological features of chronic hepatitis C (1b) in a homogeneous patient population [J].
Fanning, L ;
Kenny, E ;
Sheehan, M ;
Cannon, B ;
Whelton, M ;
O'Connell, J ;
Collins, JK ;
Shanahan, F .
HEPATOLOGY, 1999, 29 (03) :904-907
[9]   ULTRASONICALLY GUIDED FINE NEEDLE-BIOPSY OF ABDOMINAL ORGANS - INDICATIONS, RESULTS, RISKS [J].
GEBEL, M ;
HORSTKOTTE, H ;
KOSTER, C ;
BRUNKHORST, R ;
BRANDT, M ;
ATAY, Z .
ULTRASCHALL IN DER MEDIZIN, 1986, 7 (05) :198-202
[10]  
GLASER J, 1995, Z GASTROENTEROL, V33, P673