CDX2 may be a useful marker to distinguish primary ovarian carcinoid from gastrointestinal metastatic carcinoids to the ovary

被引:32
作者
Desouki, Mohamed Mokhtar [1 ]
Lloyd, Joshua [1 ]
Xu, Haodong [2 ]
Cao, Dengfeng [3 ]
Barner, Ross [4 ,5 ]
Zhao, Chengquan [1 ,5 ]
机构
[1] Univ Pittsburgh, Dept Pathol, Med Ctr, Magee Womens Hosp, Pittsburgh, PA 15213 USA
[2] Univ Rochester, Rochester, NY 14642 USA
[3] Peking Univ, Key Lab Carcinogenesis & Translat Res, Canc Hosp & Inst, Beijing 100142, Peoples R China
[4] Walter Reed Army Med Ctr, Washington, DC 20307 USA
[5] Armed Force Inst Pathol, Dept Gynecol Breast Pathol, Washington, DC USA
关键词
Ovary; Carcinoid; Immunohistochemistry; CDX2; Neuroendocrine; SERTOLI-CELL TUMOR; CLINICOPATHOLOGICAL ANALYSIS; IMMUNOHISTOCHEMICAL SURVEY; NEUROENDOCRINE TUMORS; TRANSCRIPTION; ORIGIN; GENE; EXPRESSION; INTESTINE; PULMONARY;
D O I
10.1016/j.humpath.2013.06.014
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Primary ovarian carcinoids and metastatic tumors share similar morphologic features. Metastatic carcinoids must be excluded from primary ones for prognostic and therapeutic reasons. Gastrointestinal neuroendocrine (carcinoid) tumors are much more common with the majority arising from small intestine and appendix. The aim of this study is to evaluate the role of immunohistochemistry for CDX2 in differentiating primary ovarian from metastatic carcinoids of primary gastrointestinal origin. Thirty primary pure ovarian carcinoids, 16 primary ovarian carcinoids arising in association with benign teratomas, 10 ovarian carcinoids metastatic from primary gastrointestinal tract and 70 gastrointestinal neuroendocrine tumors were studied for the expression of CDX2 by immunohistochemistry. CDX2 expression revealed that 40 (57.1%) of 70 cases of gastrointestinal carcinoids and 9 (90%) of 10 ovarian metastatic carcinoids showed positive nuclear staining (diffuse or focal). On the other hand, 3 (18.8%) of 16 primary carcinoids with teratomatous elements showed weak positivity. Among the 70 gastrointestinal carcinoids, CDX2 was positive in 38 (90.5%) of 42 cases in the duodenum, small intestine, appendix, and only in 2 (11.8%) of 17 cases of colorectal carcinoids and none of the 11 cases in the stomach. It is concluded that CDX2 may be a useful marker to distinguish primary ovarian carcinoid from metastasis from small intestinal and appendiceal neuroendocrine tumors. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:2536 / 2541
页数:6
相关论文
共 39 条
[1]  
Athavale R D, 2004, J Obstet Gynaecol, V24, P99
[2]   Ovarian mucinous carcinoids including some with a carcinomatous component - A report of 17 cases [J].
Baker, PM ;
Oliva, E ;
Young, RH ;
Talerman, A ;
Scully, RE .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (05) :557-568
[3]   Cytokeratin 7 and 20 and thyroid transcription factor 1 can help distinguish pulmonary from gastrointestinal carcinoid and pancreatic endocrine tumors [J].
Cai, YC ;
Banner, B ;
Glickman, J ;
Odze, RD .
HUMAN PATHOLOGY, 2001, 32 (10) :1087-1093
[4]   Cytokeratin 7 and cytokeratin 20 expression in epithelial neoplasms: A survey of 435 cases [J].
Chu, PG ;
Wu, E ;
Weiss, LM .
MODERN PATHOLOGY, 2000, 13 (09) :962-972
[5]   Primary ovarian carcinoid tumors [J].
Davis, KP ;
Hartmann, LK ;
Kenney, GL ;
Shapiro, H .
GYNECOLOGIC ONCOLOGY, 1996, 61 (02) :259-265
[6]   Primary insular carcinoid of the ovary [J].
Díaz-Montes, TP ;
Rosenthal, LE ;
Bristow, RE ;
Grumbine, FC .
GYNECOLOGIC ONCOLOGY, 2006, 101 (01) :175-178
[7]  
Drummond F, 1997, ANN HUM GENET, V61, P393, DOI 10.1046/j.1469-1809.1997.6150393.x
[8]   Cdx2 as a marker for neuroendocrine tumors of unknown primary sites [J].
Erickson, LA ;
Papouchado, B ;
Dimashkieh, H ;
Zhang, SY ;
Nakamura, N ;
Lloyd, RV .
ENDOCRINE PATHOLOGY, 2004, 15 (03) :247-252
[9]   The Cdx-1 and Cdx-2 homeobox genes in the intestine [J].
Freund, JN ;
Domon-Dell, C ;
Kedinger, M ;
Duluc, I .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1998, 76 (06) :957-969
[10]   The role of Cdx proteins in intestinal development and cancer [J].
Guo, RJ ;
Suh, ER ;
Lynch, JP .
CANCER BIOLOGY & THERAPY, 2004, 3 (07) :593-601