High incidence of microscopic gastrointestinal stromal tumors in the stomach

被引:335
作者
Kawanowa, Kaori
Sakuma, Yuji
Sakurai, Shinji [1 ]
Hishima, Tsunekazu
Iwasaki, Yoshiaki
Saito, Kana
Hosoya, Yoshinori
Nakajima, Takashi
Funata, Nobuaki
机构
[1] Gunma Univ, Grad Sch Med, Dept Tumor Pathol, Maebashi, Gumma 3718511, Japan
[2] Kanagawa Canc Ctr, Res Inst, Mol Pathol & Genet Div, Kanagawa 2410815, Japan
[3] Tokyo Metropolitan Komagome Hosp, Dept Pathol, Tokyo 1138677, Japan
[4] Tokyo Metropolitan Komagome Hosp, Dept Surg, Tokyo 1138677, Japan
[5] Gunma Univ, Grad Sch Med, Dept Gen Surg Sci, Maebashi, Gumma 3718511, Japan
关键词
GISTs; microscopic; stomach; incidence; c-kit;
D O I
10.1016/j.humpath.2006.07.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gastrointestinal stromal tumors (GISTs) are rare mesenchymal neoplasms with an annual incidence of approximately 10 to 20 per 1 million cases. Although pathologists have often observed incidental small GISTs in the stomach resected from patients with gastric cancer, no report on the real incidence of gastric GISTs is available. In this study, 100 whole stomachs resected from patients with gastric cancer were sectioned at 5-mm intervals and hematoxylin and eosin-stained slides (a mean of 130 slides for each case) were examined for microscopic GISTs. KIT (CD 117), CD34, and desmin expression of the incidental tumors was evaluated by immunohistochemistry, and genomic DNA extracted from formalin-fixed and paraffin-embedded tumor tissues was analyzed for c-kit gene mutations in exon 11. In 35 of the 100 whole stomachs, we found 50 microscopic GISTs, all of which were positive for KIT and/or CD34 and negative for desmin. Most microscopic GISTs (45/50, 90%) were located in the upper stomach. Two of the 25 (8%) microscopic GISTs had c-kit gene mutations. Fifty-one leiomyomas with positive expression for desmin were observed in 28 of the 100 stomachs. Both leiomyomas and GISTs were found in 12 stomachs. These results indicate that microscopic GISTs are common in the upper portion of the stomach. Considering the annual incidence of clinical GISTs, only few microscopic GISTs may grow into a clinical size with malignant potential. Further studies are required to clarify the genetic events responsible for the transformation of microscopic GISTs to clinical GISTs. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1527 / 1535
页数:9
相关论文
共 36 条
[1]  
AGAIMY A, 2005, VIRCHOWS ARCH, V25, P1
[2]   Cumulative dosage effect of a RAD51L1/HMGA2 fusion and RAD51L1 loss in a case of Pseudo-Meigs' syndrome [J].
Amant, F ;
Debiec-Rychter, M ;
Schoenmakers, EFPM ;
Hagemeijer-Hausman, A ;
Vergote, I .
GENES CHROMOSOMES & CANCER, 2001, 32 (04) :324-329
[3]   Gastrointestinal stromal tumors: A "benign" tumor with hepatic metastasis after 11 years [J].
Ballarini, C ;
Intra, M ;
Ceretti, AP ;
Prestipino, F ;
Bianchi, FM ;
Sparacio, F ;
Berti, E ;
Perrone, S ;
Silva, F .
TUMORI, 1998, 84 (01) :78-81
[4]   Loss of 14q and 22q in gastrointestinal stromal tumors (pacemaker cell tumors) [J].
Breiner, JA ;
Meis-Kindblom, J ;
Kindblom, LG ;
McComb, E ;
Lin, J ;
Nelson, M ;
Bridge, JA .
CANCER GENETICS AND CYTOGENETICS, 2000, 120 (02) :111-116
[5]   Biology of gastrointestinal stromal tumors [J].
Corless, CL ;
Fletcher, JA ;
Heinrich, MC .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (18) :3813-3825
[6]   THE EPIDEMIOLOGY OF GASTRIC-CANCER [J].
CORREA, P .
WORLD JOURNAL OF SURGERY, 1991, 15 (02) :228-234
[7]  
El-Rifai W, 2000, CANCER RES, V60, P3899
[8]  
Ernst SI, 1998, LAB INVEST, V78, P1633
[9]   Diagnosis of gastrointestinal stromal tumors: A consensus approach [J].
Fletcher, CDM ;
Berman, JJ ;
Corless, C ;
Gorstein, F ;
Lasota, J ;
Longley, BJ ;
Miettinen, M ;
O'Leary, TJ ;
Remotti, H ;
Rubin, BP ;
Shmookler, B ;
Sobin, LH ;
Weiss, SW .
HUMAN PATHOLOGY, 2002, 33 (05) :459-465
[10]   MEDICAL PROGRESS - GASTRIC-CARCINOMA [J].
FUCHS, CS ;
MAYER, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (01) :32-41