Hepatocyte antigen as a marker of intestinal metaplasia

被引:48
作者
Chu, PG
Jiang, Z
Weiss, LM
机构
[1] City Hope Natl Med Ctr, Div Pathol, Dept Pathol, Duarte, CA 91010 USA
[2] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01605 USA
关键词
hepatocyte paraffin 1; intestinal metaplasia; Barrett's esophagus; chronic gastritis; immunohistochemistry;
D O I
10.1097/00000478-200307000-00010
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Intestinal metaplasia is a histologic hallmark of Barrett's esophagus and chronic gastritis. Intestinal metaplasia may progress to dysplasia or carcinomas without proper treatment. Most cases of intestinal metaplasia are easily recognized on hematoxylin and eosin-stained sections. However, some cases of intestinal metaplasia may be hard to recognize if they lack the characteristic mucin-producing cells and Paneth cells, or if they are small in size. Recently, keratin 7, keratin 20, and MUC2 expression patterns were reported to be useful in confirming the diagnosis of intestinal metaplasia. We studied hepatocyte (Hep) antigen (a hepatocellular antigen mainly expressing in normal and neoplastic hepatic tissues) in 33 cases of Barrett's esophagus (9 cases associated with esophageal adenocarcinoma) and 13 cases of chronic gastritis associated with intestinal metaplasia and gastric adenocarcinoma. Hep monoclonal antibody recognizes intestinal metaplasia in all cases. We also compared expression of Hep with that of keratin 7, keratin 20, and MUC2 in intestinal metaplasia. The specificity and sensitivity of Hep for intestinal metaplasia were higher than that of keratin 7 and keratin 20, or MUC2. We conclude that Hep may be used as a single diagnostic marker for intestinal metaplasia.
引用
收藏
页码:952 / 959
页数:8
相关论文
共 34 条
[1]   Mucin gene expression in Barrett's oesophagus: an in situ hybridisation and immunohistochemical study [J].
Arul, GS ;
Moorghen, M ;
Myerscough, N ;
Alderson, DA ;
Spicer, RD ;
Corfield, AP .
GUT, 2000, 47 (06) :753-761
[2]  
BARA J, 1986, CANCER RES, V46, P3983
[3]   Non-goblet cell population of Barrett's esophagus: An immunohistochemical demonstration of intestinal differentiation [J].
Chaves, P ;
Cardoso, P ;
de Almeida, JCM ;
Pereira, AD ;
Leitao, CN ;
Soares, J .
HUMAN PATHOLOGY, 1999, 30 (11) :1291-1295
[4]  
Chinyama CN, 1999, HISTOPATHOLOGY, V35, P517
[5]   Hepatocyte antigen as a marker of hepatocellular carcinoma - An immunohistochemical comparison to carcinoembryonic antigen, CD10, and alpha-fetoprotein [J].
Chu, PGG ;
Ishizawa, S ;
Wu, E ;
Weiss, LM .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (08) :978-988
[6]  
Conio M, 2001, Gastrointest Endosc, V54, P799
[7]   Cytokeratin immunoreactivity of intestinal metaplasia at normal oesophagogastric junction indicates its aetiology [J].
Couvelard, A ;
Cauvin, JM ;
Goldfain, D ;
Rotenberg, A ;
Robaszkiewicz, M ;
Fléjou, JF .
GUT, 2001, 49 (06) :761-766
[8]   DETECTION OF A SHARED COLON EPITHELIAL EPITOPE ON BARRETT EPITHELIUM BY A NOVEL MONOCLONAL-ANTIBODY [J].
DAS, KM ;
PRASAD, I ;
GARLA, S ;
AMENTA, PS .
ANNALS OF INTERNAL MEDICINE, 1994, 120 (09) :753-756
[9]  
Filipe M. I., 1986, GASTRIC CARCINOMA, P87
[10]   Phenotype of Barrett's esophagus and intestinal metaplasia of the distal esophagus and gastroesophageal junction - An immunohistochemical study of cytokeratins 7 and 20, Das-1 and 45MI [J].
Glickman, JN ;
Wang, H ;
Das, KM ;
Goyal, RK ;
Spechler, SJ ;
Antonioli, D ;
Odze, RD .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (01) :87-94