Gastrointestinal stromal tumors: Pathology and prognosis at different sites

被引:1768
作者
Miettinen, Markku [1 ]
Lasota, Jerzy [1 ]
机构
[1] Armed Forces Inst Pathol, Dept Soft Tissue Pathol, Washington, DC 20306 USA
关键词
stomach; small intestine; extragastrointestinal GIST; prognosis; histopathology inummohistochemical markers;
D O I
10.1053/j.semdp.2006.09.001
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 [基础医学];
摘要
Gastrointestinal (GI) stromal tumors (GISTs) are the most common mesenchymal tumors specific to the GI tract, generally defined as KIT (CD117)-positive tumors with a characteristic set of histologic features. These tumors, derived from Cajal cells or their precursors, most commonly occur at the age >50 years in the stomach (60%), jejunum and ileum (30%), duodenum (4-5%), rectum (4%), colon and appendix (1-2%), and esophagus (< 1%), and rarely as apparent primary extragastrointestinal tumors in the vicinity of stomach or intestines. Their overall incidence has been estimated as 10 to 20 per million, including incidental minimal tumors. GISTs are rare in children (<1%) and almost exclusively occur in stomach. They are common in patients with neurofibromatosis 1, who have a predisposition to (multiple) small intestinal GISTs. GISTs contain a spectrum from minute indolent tumors to sarcomas at all sites of occurrence. Their gross patterns are diverse, including nodular, cystic, and diverticular tumors. External involvement of pancreas and liver can simulate primary tumor in these organs. In general, gastric tumors have a more favorable prognosis than the intestinal ones with similar parameters. Gastric GISTs <= 10 cm and <= 5 mitoses per 50 HPFs have a low risk for metastasis, whereas those with >5 per 50 HPFs and >5 em in diameter have a high risk for metastasis. In contrast, all intestinal GISTs >5 cm independent of mitotic rate have at least moderate risk for metastases, and all >5 mitoses per 50 HPFs have a high risk for metastases. Intestinal GISTs <= 5 cm with <= 5 mitoses per 50 HPFs have a low risk for metastases. Gastric GISTs can be divided into histologic subgroups including 4 spindle cell and 4 epithelioid variants. Intestinal GISTs are a histologically more homogeneous group and often contain distinctive extracellular collagen globules, skeinoid fibers. Immunohistochemical demonstration of KIT, CD34, or protein kinase theta positivity helps to properly identify these tumors. (C) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:70 / 83
页数:14
相关论文
共 92 条
[1]
ABRAHAM SC, 2006, MOD PATHOL, V19, pA100
[2]
Agaimy A, 2006, LANGENBECKS ARCH SUR
[3]
p53 expression in gastrointestinal stromal tumors [J].
Al-Bozom, IA .
PATHOLOGY INTERNATIONAL, 2001, 51 (07) :519-523
[4]
NF1-associated gastrointestinal stromal tumors have unique clinical, phenotypic and genotypic characteristics [J].
Andersson, J ;
Sihto, H ;
Meis-Kindblom, JM ;
Joensuu, H ;
Nupponen, N ;
Kindblom, LG .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (09) :1170-1176
[5]
Gene expression in gastrointestinal stromal tumors is distinguished by KIT genotype and anatomic site [J].
Antonescu, CR ;
Viale, A ;
Sarran, L ;
Tschernyavsky, SJ ;
Gonen, M ;
Segal, NH ;
Maki, RG ;
Socci, ND ;
DeMatteo, RP ;
Besmer, P .
CLINICAL CANCER RESEARCH, 2004, 10 (10) :3282-3290
[6]
APPELMAN HD, 1976, CANCER, V38, P708, DOI 10.1002/1097-0142(197608)38:2<708::AID-CNCR2820380215>3.0.CO
[7]
2-6
[8]
Protein kinase C θ is highly expressed in gastrointestinal stromal tumors but not in other mesenchymal neoplasias [J].
Blay, P ;
Astudillo, A ;
Buesa, JM ;
Campo, E ;
Abad, M ;
García-García, J ;
Miquel, R ;
Marco, V ;
Sierra, M ;
Losa, R ;
Lacave, A ;
Braña, A ;
Balbín, M ;
Freije, JMP .
CLINICAL CANCER RESEARCH, 2004, 10 (12) :4089-4095
[9]
Stromal tumors of the jejunum and ileum - A clinicopathologic study of 39 cases [J].
Brainard, JA ;
Goldblum, JR .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (04) :407-416
[10]
Ki67 protein: the immaculate deception? [J].
Brown, DC ;
Gatter, KC .
HISTOPATHOLOGY, 2002, 40 (01) :2-11