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Title: More differences between HNPCC-related and sporadic carcinomas from the endometrium as compared to the colon.
Author(s): Bos, M.
Hoven, M. van
Jongejan, E.
Leij, F. van der
Michels, M.
Schakenraad, S.
Aben, K.K.H. (217174302)
Hoogerbrugge-van der Linden, N. (101110200)
Ligtenberg, M.J.L. (088914763)
Krieken, J.H.J.M. van (071431772)
Publication year: 2004
Document type: Article / Letter to editor
Journal: American Journal of Surgical Pathology
ISSN: 0147-5185
Volume: vol. 28
Issue: iss. 6
Start page: p. 706
End page: p. 711
Abstract: PURPOSE: Recognition of hereditary nonpolyposis colorectal cancer (HNPCC)-related endometrial carcinoma from sporadic carcinoma by histologic features as compared with colonic cases. STUDY DESIGN: Case-control study. METHODS AND MATERIALS: From the files of the Nijmegen Hereditary Cancer Clinic, HNPCC-related (n = 6) endometrial and colorectal (n = 18) carcinomas were selected. For every HNPCC-related tumor, 2 sporadic control cases were included. The tumors were evaluated for the following 7 pathologic features: tumor differentiation, T-stage, growth pattern, presence of Crohn-like lymphoid reaction, mucinous differentiation, presence of lymphangioinvasive growth, and the amount of tumor-infiltrating lymphocytes. RESULTS: HNPCC-related endometrial carcinomas were significantly more often poorly differentiated (83% versus 27%), more often showed the presence of a Crohn-like lymphoid reaction (100% versus 13%) and lymphangioinvasive growth (67% versus 0%), and high number of tumor-infiltrating lymphocytes were more often present (100% versus 36%) compared with sporadic endometrial carcinomas. The differences between HNPCC and sporadic colorectal cancer specimens were less discriminating. CONCLUSIONS: HNPCC-related endometrial carcinomas are characterized by poor differentiation, more frequent Crohn-like lymphoid reaction, lymphangioinvasive growth and more tumor-infiltrating lymphocytes. These features therefore might form the basis for selecting patients for counseling in a hereditary cancer clinic or testing for microsatellite instability or mutation analysis of mismatch repair genes, especially when they are of relatively young age.
Subject: EBP 1: Determinants in Health and Disease
UMCN 1.2: Molecular diagnosis, prognosis and monitoring
UMCN 1.3: Tumor microenvironment
UMCN 1.5: Interventional oncology
UMCN 5.4: Renal disorders
Organization: UMCN Extern
Obstetrics and Gynaecology
Epidemiology, Biostatistics & HTA
Human Genetics
Pathology
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/57393

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