Gastric polyps: an update of their pathology and biological significance

被引:82
作者
Oberhuber, G
Stolte, M
机构
[1] Univ Vienna, Sch Med, Dept Clin Pathol, A-1090 Vienna, Austria
[2] Klinikum Bayreuth, Dept Pathol, D-95445 Bayreuth, Germany
关键词
gastric polyps; adenoma; carcinoma; non-neoplastic polyps;
D O I
10.1007/s004280000330
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gastric polyps are clinically important lesions that are frequently encountered in routine pathology (2-3% of all gastroscopies). Polyps may occur sporadically or in polyposis syndromes, such as familial adenomatous polyposis coli (FAP), Peutz-Jeghers syndrome, juvenile polyposis, Cowden's disease and Cronkhite-Canada syndrome. In biopsy specimens taken during routine gastroscopic examinations, it is almost always possible to differentiate between neoplastic and non-neoplastic polyps and to type polyps. In this review, we focus on the morphological spectrum of gastric polyps in an attempt to assist the pathologist and the gastroenterologist in recognising the lesion and in treating patients with gastric polyps, respectively. Further, we propose that the World Health Organization (WHO) classification should be modified to include the following categories: non-neoplastic polyps (WHO: tumour-like lesion), ham artomatous polyps/polyps of polyposis syndromes (WHO: tumour-like lesion), heterotopic tissue polyps (WHO: tumour-like lesion), neoplastic polyps (WHO: epithelial, non-epithelial and endocrine tumours) and reactive polypoid lesions.
引用
收藏
页码:581 / 590
页数:10
相关论文
共 85 条
[21]   GASTRIC POLYPS [J].
FABRY, TL ;
FRANKEL, A ;
WAYE, JD .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1982, 4 (01) :23-27
[22]   DIFFERENTIATION AND RISK ASSESSMENT OF GASTROINTESTINAL STROMAL TUMORS [J].
FRANQUEMONT, DW .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1995, 103 (01) :41-47
[23]   ENDOSCOPIC GASTRODUODENAL POLYPECTOMY [J].
GHAZI, A ;
FERSTENBERG, H ;
SHINYA, H .
ANNALS OF SURGERY, 1984, 200 (02) :175-180
[24]  
Ginsberg GG, 1996, AM J GASTROENTEROL, V91, P714
[25]   IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE [J].
GRODEN, J ;
THLIVERIS, A ;
SAMOWITZ, W ;
CARLSON, M ;
GELBERT, L ;
ALBERTSEN, H ;
JOSLYN, G ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :589-600
[27]   A serine/threonine kinase gene defective in Peutz-Jegheus syndrome [J].
Hemminki, A ;
Markie, D ;
Tomlinson, I ;
Avizienyte, E ;
Roth, S ;
Loukola, A ;
Bignell, G ;
Warren, W ;
Aminoff, M ;
Höglund, P ;
Järvinen, H ;
Kristo, P ;
Pelin, K ;
Ridanpää, M ;
Salovaara, R ;
Toro, T ;
Bodmer, W ;
Olschwang, S ;
Olsen, AS ;
Stratton, MR ;
de la Chapelle, A ;
Aaltonen, LA .
NATURE, 1998, 391 (6663) :184-187
[28]   GASTROINTESTINAL MANIFESTATIONS OF COWDENS-DISEASE - REPORT OF 4 CASES [J].
HIZAWA, K ;
IIDA, M ;
MATSUMOTO, T ;
KOHROGI, N ;
SUEKANE, H ;
YAO, T ;
FUJISHIMA, M .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1994, 18 (01) :13-18
[29]  
HOFTING I, 1993, LEBER MAGEN DARM, V23, P107
[30]  
HOFTING I, 1993, Z GASTROENTEROL, V31, P480