Role of liver biopsy in nonalcoholic fatty liver disease

被引:1
作者
ILKe Nalbantoglu [1 ]
Elizabeth M Brunt [1 ]
机构
[1] Department of Pathology and Immunology, Washington University School of Medicine,Saint Louis, MO 63110, United States
关键词
Nonalcoholic fatty liver disease; Nonalcoholic steatohepatitis; Liver biopsy; Histopathology; Grading and staging;
D O I
暂无
中图分类号
R575.5 [肝代谢障碍];
学科分类号
1002 ; 100201 ;
摘要
Nonalcoholic fatty liver disease(NAFLD), defined as abnormal accumulation(> 5%) of hepatic triglyceride without excess alcohol intake, is the most common form of chronic liver disease in adults and children in the United States. NAFLD encompasses a spectrum of histologic findings including uncomplicated steatosis, steatosis with inflammation and steatohepatitis [nonalcoholic steatohepatitis(NASH)]; the latter can advance to cirrhosis and hepatocellular carcinoma. NASH is currently accepted as the hepatic manifestation of the set of cardiovascular risk factors collectively known as metabolic syndrome. In 1999 a system for histologic grading and staging for NASH was proposed; this was revised by the NASH Clinical Research Network in 2005 for the entire spectrum of lesions in NAFLD, including the lesions and patterns of pediatric NAFLD, and for application in clinical research trials. Diagnosis remains distinct from grade and stage. A recent European proposal separates steatosis from activity to derive a numeric diagnosis of NASH. Even though there have been promising advancements in non-invasive testing, these tests are not yet detailed enough to replace the full range of findings provided by liver biopsy evaluation. Limitations of biopsy are acknowledged, but liver biopsy remains the "gold standard" for diagnosis and determination of amounts of necroinflammatory activity, and location of fibrosis, as well as remodeling of the parenchyma in NASH. This review focuses on the specific histologic lesions of NAFLD and NASH, grading and staging, differential diagnoses to be considered, and the continuing role of the liver biopsy in this important liver disease.
引用
收藏
页码:9026 / 9037
页数:12
相关论文
共 62 条
[41]   Histologic variation of grade and stage of nonalcoholic fatty liver disease in liver biopsies [J].
Janiec, DJ ;
Jacobson, ER ;
Freeth, A ;
Spaulding, L ;
Blaszyk, H .
OBESITY SURGERY, 2005, 15 (04) :497-501
[42]  
Nonalcoholic steatohepatitis: Histologic features and clinical correlations with 30 blinded biopsy specimens[J] . Elizabeth M. Brunt,Brent A. Neuschwander-Tetri,Dana Oliver,Kent R. Wehmeier,Bruce R. Bacon.Human Pathology . 2004 (9)
[43]  
The histological course of nonalcoholic fatty liver disease: a longitudinal study of 103 patients with sequential liver biopsies[J] . Leon A. Adams,Schuyler Sanderson,Keith D. Lindor,Paul Angulo.Journal of Hepatology . 2004 (1)
[44]  
Silent non-alcoholic fatty liver disease—a clinical–histological study[J] . Paolo Sorrentino,Giovanni Tarantino,Paolo Conca,Alessandro Perrella,Maria Luigi Terracciano,Raffaella Vecchione,Giovanna Gargiulo,Nicola Gennarelli,Roberto Lobello.Journal of Hepatology . 2004 (5)
[45]   Nonalcoholic steatohepatitis [J].
Brunt, EM .
SEMINARS IN LIVER DISEASE, 2004, 24 (01) :3-20
[46]  
Nonalcoholic steatohepatitis: Summary of an AASLD Single Topic Conference[J] . Brent A. Neuschwander‐Tetri,Stephen H. Caldwell.Hepatology . 2003 (5)
[47]   Hepatocyte apoptosis and Fas expression are prominent features of human nonalcoholic steatohepatitis [J].
Feldstein, AE ;
Canbay, A ;
Angulo, P ;
Taniai, M ;
Burgart, LJ ;
Lindor, KD ;
Gores, GJ .
GASTROENTEROLOGY, 2003, 125 (02) :437-443
[48]   Oxidative stress and oval cell accumulation in mice and humans with alcoholic and nonalcoholic fatty liver disease [J].
Roskams, T ;
Yang, SQ ;
Koteish, A ;
Durnez, A ;
DeVos, R ;
Huang, XW ;
Achten, R ;
Verslype, C ;
Diehl, AM .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (04) :1301-1311
[49]   Nonalcoholic fatty liver disease in patients with hepatitis C is associated with features of the metabolic syndrome [J].
Sanyal, AJ ;
Contos, MJ ;
Sterling, RK ;
Luketic, VA ;
Shiffman, ML ;
Stravitz, RT ;
Mills, AS .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (09) :2064-2071
[50]   Improved nonalcoholic steatohepatitis after 48 weeks of treatment with the PPAR-γ ligand rosiglitazone [J].
Neuschwander-Tetri, BA ;
Brunt, EM ;
Wehmeier, KR ;
Oliver, D ;
Bacon, BR .
HEPATOLOGY, 2003, 38 (04) :1008-1017