C-KIT in gastrointestinal stromal tumors and associated malignancies: A Study in a population with genetic isolation

被引:0
作者
Rodriguez-Gonzalez, Diana [1 ]
Delgado-Plasencia, Luciano [1 ]
Hernandez-Leon, Carmen [2 ]
Torres-Monzon, Esther [3 ]
Elisa Castro-Peraza, Maria [1 ]
Cruz-Jurado, Josefina [4 ]
Bravo-Gutierrez, Alberto [1 ]
Medina-Arana, Vicente [1 ]
机构
[1] Hosp Univ Canarias, Serv Cirugia Gen & Digest, Santa Cruz De Tenerife, Spain
[2] Hosp Univ Canarias, Serv Anat Patol, Santa Cruz De Tenerife, Spain
[3] Hosp Univ Canarias, Serv Radiol, Santa Cruz De Tenerife, Spain
[4] Hosp Univ Canarias, Med Oncol Serv, La Cuesta, Santa Cruz De T, Spain
来源
GASTROENTEROLOGIA Y HEPATOLOGIA | 2015年 / 38卷 / 08期
关键词
Gastrointestinal stromal tumor; Associated neoplasm; CD; 117; Genetic isolation; SYNCHRONOUS COLORECTAL ADENOCARCINOMA; CELL CARCINOMA; EXPRESSION; COEXISTENCE; DIAGNOSIS; MUTATION;
D O I
10.1016/j.gastrohep.2015.02.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Gastrointestinal stromal tumors (GIST) are the most common mesenchymal tumors of the gastrointestinal tract. Numerous studies have reported the association between GIST and other neoplasms. Objectives: The aim of this study was to investigate the possible association between GIST and other tumors in a genetically isolated population. Methods: A retrospective study was conducted of patients with GIST between 2002 and 2009 at our center. Epidemiological, pathological and family data in patients with GIST alone (group A) were compared with those in patients with GIST associated with other neoplasms (group B). A possible common genetic mechanism was investigated between GIST and associated malignancies by testing the detection of the immunohistochemical marker, CD117, in all tumors. Results: Twenty-two patients with GIST were identified, 10 in group A (45%) and 12 in group B (55%). In group B, the associated tumor was malignant in 6 patients (50%) and benign in another 6.(50%). Of the 22 patients with GIST, 8 (36%) had a family history of malignancies. Of these 8 patients, 7 (87.5%) were in group B (p = 0.03) and 3 (37.5%) showed the same pathological type of neoplasm as their relatives. All GIST were positive for CD117 whereas associated malignancies were negative for this marker. Conclusion: We did not find immunohistochemical positivity for CD117 in malignancies associated with GIST. Given the special characteristics of the study population, the association between GIST and associated malignancies may be incidental. (C) 2015 Elsevier Espana, S.L.U. and AEEH y AEG. All rights reserved.
引用
收藏
页码:484 / 490
页数:7
相关论文
共 50 条
  • [31] Fluorescence in Situ Hybridization Analysis and Immunophenotyping of c-Kit/PDGFRA and BcI-2 Expression in Gastrointestinal Stromal Tumors
    Orsenigo, Marta
    Brich, Silvia
    Riva, Carla
    Conca, Elena
    Bertulli, Rossella
    Dileo, Palma
    Gronchi, Alessandro
    Casali, Paolo G.
    Pierotti, Marco A.
    Tamborini, Elena
    Pilotti, Silvana
    ANALYTICAL AND QUANTITATIVE CYTOLOGY AND HISTOLOGY, 2010, 32 (04): : 225 - 233
  • [32] Characterization of novel germline c-kit gene mutation, KIT-Tyr553Cys, observed in a family with multiple gastrointestinal stromal tumors
    Nakai, Mayumi
    Hashikura, Yuka
    Ohkouchi, Mizuka
    Yamamura, Masahiro
    Akiyama, Takashi
    Shiba, Kazuhiro
    Kajimoto, Noriko
    Tsukamoto, Yoshitane
    Hao, Hiroyuki
    Isozaki, Koji
    Hirai, Toshihiro
    Hirota, Seiichi
    LABORATORY INVESTIGATION, 2012, 92 (03) : 451 - 457
  • [33] Rectal gastrointestinal stromal tumors associated with a novel germline KIT mutation
    Wozniak, Agnieszka
    Rutkowski, Piotr
    Sciot, Raf
    Ruka, Wtodzimierz
    Michej, Wanda
    Debiec-Rychter, Maria
    INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (09) : 2160 - 2164
  • [34] Interstitial cells of Cajal do not harbor c-kit or PDGFRA gene mutations in patients with sporadic gastrointestinal stromal tumors
    Takahiko Nakajima
    Shigeharu Miwa
    Takayuki Ando
    Haruka Fujinami
    Shinya Kajiura
    Ayumu Hosokawa
    Yasuo Takano
    Toshiro Sugiyama
    Journal of Gastroenterology, 2009, 44 : 426 - 431
  • [35] C-KIT mutations were closely associated with the response to Imatinib in Chinese advanced gastrointestinal stromal tumor patients
    Jing Gao
    Yunzhi Dang
    Naiping Sun
    Jian Li
    Lin Shen
    Medical Oncology, 2012, 29 : 3039 - 3045
  • [36] Detection of c-KIT and PDGFRA Gene Mutations in Gastrointestinal Stromal Tumors Comparison of DHPLC and DNA Sequencing Methods Using a Single Population-Based Cohort
    Battochio, Angeline
    Mohammed, Shamayel
    Winthrop, Debra
    Lefresne, Shilo
    Mulder, Karen
    Chu, Quincy
    O'Hara, Carolyn
    Lai, Raymond
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2010, 133 (01) : 149 - 155
  • [37] Biology and genetic aspects of gastrointestinal stromal tumors: KIT activation and cytogenetic alterations
    Heinrich, MC
    Rubin, BP
    Longley, BJ
    Fletcher, JA
    HUMAN PATHOLOGY, 2002, 33 (05) : 484 - 495
  • [38] Frequent c-Kit gene mutations not only in gastrointestinal stromal tumors but also in interstitial cells of Cajal in surrounding normal mucosa
    Ogasawara, N
    Tsukamoto, T
    Inada, K
    Mizoshita, T
    Ban, N
    Yamao, K
    Joh, T
    Itoh, M
    Tatematsu, M
    CANCER LETTERS, 2005, 230 (02) : 199 - 210
  • [39] Fine-needle aspiration biopsy diagnosis of gastrointestinal stromal tumors using morphology, immunocytochemistry, and mutational analysis of c-kit
    Rader, AE
    Avery, A
    Wait, CL
    McGreevey, LS
    Faigel, D
    Heinrich, MC
    CANCER CYTOPATHOLOGY, 2001, 93 (04) : 269 - 275
  • [40] Study of c-kit immunoexpression in canine cutaneous melanocytic tumors
    Gomes, Joana
    Queiroga, Felisbina L.
    Prada, Justina
    Pires, Isabel
    MELANOMA RESEARCH, 2012, 22 (03) : 195 - 201