Fibrosis heterogeneity in nonalcoholic steatohepatitis and Hepatitis C virus needle core biopsy specimens

被引:6
作者
Goldstein, NS
Hastah, F
Galan, MV
Gordon, SC
机构
[1] William Beaumont Hosp, Dept Anat Pathol, Royal Oak, MI 48073 USA
[2] William Beaumont Hosp, Dept Gastroenterol Hepatol, Royal Oak, MI 48073 USA
关键词
liver; fibrosis; nonalcoholic steatohepatitis; NASH; Hepatitis C virus; HCV; scoring; cirrhosis;
D O I
10.1309/EY72F1EN0XCB1KXX
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We examined 46 nonalcoholic steatohepatitis (NASH) and 52 hepatitis C virus (HCV) biopsy specimens to determine the magnitude of fibrosis heterogeneity and minimum length for accurate fibrosis staging. Three fibrosis scores were recorded: lowest regional, highest regional, and most common overall. Mean specimen lengths were 1.6 and 1.8 cm in NASH and HCV, respectively (P = .283). Mean (highest minus lowest)fibrosis heterogeneity scores (highest regional fibrosis minus lowest regional fibrosis) were 3.7 and 2.0 in NASH and HCV, respectively (P < .001). Of 36 NASH specimens longer than 1.0 cm, 31 (86%) had the highest regional fibrosis in the deepest sampled parenchyma. Shorter specimens were associated significantly with greater fibrosis heterogeneity in NASH (coefficient, -1.3; P < .001) but not in HCV (P = .901). NASH specimens longer than 1.6 cm had significantly lower mean heterogeneity scores than specimens 1.6 cm or shorter (1.2 vs 3.4; P =.012). In NASH, fibrosis heterogeneity can be substantial and is greater than in HCV, and parenchymal injury, fibrosis, and healing might vary in different regions of the liver The fibrosis stage in patients with NASH might not be assessed accurately in short specimens. Individual needle cores should be longer than 1.6 cm in NASH for accurate fibrosis staging.
引用
收藏
页码:382 / 387
页数:6
相关论文
共 39 条
  • [1] SAMPLING VARIABILITY ON PERCUTANEOUS LIVER-BIOPSY
    ABDI, W
    MILLAN, JC
    MEZEY, E
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1979, 139 (06) : 667 - 669
  • [2] Clinical hepatic impairment after the duodenal switch
    Baltasar, A
    Serra, C
    Pérez, N
    Bou, R
    Bengochea, M
    [J]. OBESITY SURGERY, 2004, 14 (01) : 77 - 83
  • [3] Sampling variability of liver fibrosis in chronic hepatitis C
    Bedossa, P
    Dargère, D
    Paradis, V
    [J]. HEPATOLOGY, 2003, 38 (06) : 1449 - 1457
  • [4] Steatohepatitis-inducing drugs cause mitochondrial dysfunction and lipid peroxidation in rat hepatocytes
    Berson, A
    De Beco, V
    Lettéron, P
    Robin, MA
    Moreau, C
    El Kahwaji, J
    Verthier, N
    Feldmann, G
    Fromenty, B
    Pessayre, D
    [J]. GASTROENTEROLOGY, 1998, 114 (04) : 764 - 774
  • [5] Nonalcoholic steatohepatitis: A proposal for grading and staging the histological lesions
    Brunt, EM
    Janney, CG
    Di Bisceglie, AM
    Neuschwander-Tetri, BA
    Bacon, BR
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 1999, 94 (09) : 2467 - 2474
  • [6] Pathology of steatohepatitis
    Brunt, EM
    Tiniakos, DG
    [J]. BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2002, 16 (05) : 691 - 707
  • [7] Nonalcoholic steatohepatitis: Definition and pathology
    Brunt, EM
    [J]. SEMINARS IN LIVER DISEASE, 2001, 21 (01) : 3 - 16
  • [8] Liver transplantation in a case of steatohepatitis and subacute hepatic failure after biliopancreatic diversion for morbid obesity
    Castillo, J
    Fábrega, E
    Escalante, CF
    Sanjuan, JCR
    Herrera, L
    Hernánz, F
    Martino, E
    Casafont, F
    Fleitas, MG
    [J]. OBESITY SURGERY, 2001, 11 (05) : 640 - 642
  • [9] Nonalcoholic fatty liver disease
    Clark, JM
    Brancati, FL
    Diehl, AM
    [J]. GASTROENTEROLOGY, 2002, 122 (06) : 1649 - 1657
  • [10] Impact of liver biopsy size on histological evaluation of chronic viral hepatitis: the smaller the sample, the milder the disease
    Colloredo, G
    Guido, M
    Sonzogni, A
    Leandro, G
    [J]. JOURNAL OF HEPATOLOGY, 2003, 39 (02) : 239 - 244