Histopathological diagnosis of ulcerative colitis-associated neoplasia

被引:31
作者
Kawachi, Hiroshi [1 ]
机构
[1] JFCR, Dept Pathol, Canc Inst Hosp, Tokyo, Japan
关键词
colorectal cancer; Histopathological diagnosis; dysplasia; neoplasia; ulcerative colitis; INFLAMMATORY-BOWEL-DISEASE; CLINICAL-PRACTICE GUIDELINES; P53; EXPRESSION; DYSPLASIA; CANCER; CLASSIFICATION; INTEROBSERVER; OBSERVER;
D O I
10.1111/den.13387
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In patients with ulcerative colitis, tumor development occurs with an increase in the duration of the disease. Such lesions, known as ulcerative colitis-associated neoplasia (UCAN), histologically show a broad variety of findings such as low-grade dysplasia, high-grade dysplasia, and invasive carcinoma. For pathologists, however, the histopathological diagnosis of UCAN is occasionally difficult. Problems in pathological diagnosis can be summarized into the following three categories: (i) difficulty in discriminating UCAN from non-neoplastic inflammatory change; (ii) difficulty in discriminating UCAN from sporadic epithelial neoplasm; and (iii) difficulty in histological grading of UCAN. For most lesions, pathologists can make conclusive histological diagnoses without any problems. However, pathologists occasionally face diagnostic difficulties, especially in cases of lesions with borderline or indefinite histology and, therefore, at least two experienced gastrointestinal pathologists are needed to confirm the diagnosis. Hence, a confirmation is usually preferable for the estimation of tumor depth and lymphovascular invasion in digestive tract cancers as well as in UCAN. Immunohistochemistry for p53 and Ki-67 (MIB-1) is occasionally useful as an ancillary tool. Since UCAN has distinct characteristics compared to sporadic epithelial neoplasia, its treatment strategy should be carefully discussed by a multidisciplinary team, especially for cases of lesions with indefinite histology. At present, although surgical intervention such as total colectomy is the most promising procedure for UCAN, recent advances in endoscopic diagnosis and therapy are expected to improve future treatment strategy.
引用
收藏
页码:31 / 35
页数:5
相关论文
共 28 条
[1]   Endoscopy/surveillance in inflammatory bowel disease [J].
Ahmadi, Anis A. ;
Polyak, Steven .
SURGICAL CLINICS OF NORTH AMERICA, 2007, 87 (03) :743-+
[2]   Inter-observer and intra-observer variability in the diagnosis of dysplasia in patients with inflammatory bowel disease: correlation of pathological and endoscopic findings [J].
Allende, D. ;
Elmessiry, M. ;
Hao, W. ;
DaSilva, G. ;
Wexner, S. D. ;
Bejarano, P. ;
Berho, M. .
COLORECTAL DISEASE, 2014, 16 (09) :710-718
[3]   Precancer in ulcerative colitis: the role of the field effect and its clinical implications [J].
Baker, Kathryn T. ;
Salk, Jesse J. ;
Brentnall, Teresa A. ;
Risques, Rosa Ana .
CARCINOGENESIS, 2018, 39 (01) :11-20
[4]  
BLACKSTONE MO, 1981, GASTROENTEROLOGY, V80, P366
[5]   OBSERVER VARIATION IN THE ASSESSMENT OF DYSPLASIA IN ULCERATIVE-COLITIS [J].
DIXON, MF ;
BROWN, LJR ;
GILMOUR, HM ;
PRICE, AB ;
SMEETON, NC ;
TALBOT, IC ;
WILLIAMS, GT .
HISTOPATHOLOGY, 1988, 13 (04) :385-397
[6]   Inter-observer variation between general and specialist gastrointestinal pathologists when grading dysplasia in ulcerative colitis [J].
Eaden, J ;
Abrams, K ;
McKay, H ;
Denley, H ;
Mayberry, J .
JOURNAL OF PATHOLOGY, 2001, 194 (02) :152-157
[7]  
Hirata I, 2008, STOMACH INTESTINE, V43, P1273
[8]  
Jain D., 2013, MORSON DAWSONS GASTR, P552, DOI [10.1002/9781118399668.ch35, DOI 10.1002/9781118399668.CH35]
[9]   Risk of Colorectal Cancer in Patients With Ulcerative Colitis: A Meta-analysis of Population-Based Cohort Studies [J].
Jess, Tine ;
Rungoe, Christine ;
Peyrin-Biroulet, Laurent .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2012, 10 (06) :639-645
[10]   p53 Expression as a Diagnostic Biomarker in Ulcerative Colitis-Associated Cancer [J].
Kobayashi, Kazuhiro ;
Tomita, Hiroyuki ;
Shimizu, Masahito ;
Tanaka, Takuji ;
Suzui, Natsuko ;
Miyazaki, Tatsuhiko ;
Hara, Akira .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (06)