WT-1 assists in distinguishing ovarian from uterine serous carcinoma and in distinguishing between serous and endometrioid ovarian carcinoma

被引:170
作者
Al-Hussaini, M
Stockman, A
Foster, H
McCluggage, WG
机构
[1] Royal Grp Hosp Trust, Dept Pathol, Belfast BT12 6BL, Antrim, North Ireland
[2] Belfast City Hosp Trust, Dept Pathol, Belfast, Antrim, North Ireland
关键词
ovary; serous carcinoma; uterine serous carcinoma; endometrioid carcinoma; serous borderline tumour; primary peritoneal serous carcinoma; WT-1; immunohistochemistry;
D O I
10.1111/j.1365-2559.2004.01787.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: It has been suggested that WT-1 is helpful in distinguishing a primary ovarian serous carcinoma (OSC) from a primary uterine serous carcinoma (USC). Since both neoplasms are often disseminated at diagnosis and since USC often spreads to the ovary and vice versa, it may be difficult to ascertain the primary site. This is important, since adjuvant therapies for OSC and USC may differ. WT-1 staining patterns also differ between OSC and ovarian endometrioid carcinoma and so it is possible that WT-1 may assist in the distinction of these two neoplasms, which is sometimes problematic, especially with poorly differentiated tumours. This study aims to document the value of WT-1 in these settings. Cases of ovarian borderline serous tumour, primary peritoneal serous carcinoma (PPSC) and uterine endometrioid carcinoma were also studied. Methods and results: Cases of OSC (n = 38), USC (n = 25) (in five of these cases there was also a component of endometrioid adenocarcinoma), ovarian endometrioid carcinoma (n = 13), uterine endometrioid carcinoma (n = 7), ovarian borderline serous tumour (n = 16) and PPSC (n = 6) were stained with WT-1. Cases were scored on a scale of 0-3, depending on the percentage of positive cells. The intensity of staining was scored as weak, moderate or strong. There was positive nuclear stainingof 36 of 38 (94.7%) OSC with WT-1. In most OSC (68.4%), >50% of cells stained positively and staining was usually strong. Five of 25 (20%) USC were positive with only two cases exhibiting staining of >50% of cells. All primary ovarian and uterine endometrioid carcinomas were negative. All PPSC were positive, usually with diffuse strong immunoreactivity. Fourteen of 16 borderline serous tumours exhibited positivity with WT-1. Conclusions: WT-1 is useful in distinguishing OSC (characteristically diffuse strong nuclear positivity) from USC (characteristically negative). However, rarely OSC is negative and occasional cases of USC are positive. WT-1 may also be helpful in differentiating poorly differentiated OSC from poorly differentiated ovarian endometrioid carcinoma.
引用
收藏
页码:109 / 115
页数:7
相关论文
共 29 条
[1]   ENDOMETRIAL INTRAEPITHELIAL CARCINOMA - A DISTINCTIVE LESION SPECIFICALLY ASSOCIATED WITH TUMORS DISPLAYING SEROUS DIFFERENTIATION [J].
AMBROS, RA ;
SHERMAN, ME ;
ZAHN, CM ;
BITTERMAN, P ;
KURMAN, RJ .
HUMAN PATHOLOGY, 1995, 26 (11) :1260-1267
[2]  
AMIN KM, 1995, AM J PATHOL, V146, P344
[3]   Early uterine serous carcinoma: Clonal origin of extrauterine disease [J].
Baergen, RN ;
Warren, CD ;
Isacson, C ;
Ellenson, LH .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 2001, 20 (03) :214-219
[4]   Micropapillary serous carcinoma of the ovary - A distinctive low-grade carcinoma related to serous borderline tumors [J].
Burks, RT ;
Sherman, ME ;
Kurman, RJ .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (11) :1319-1330
[5]   Immunohistochemical detection of the Wilms' tumour gene WT1 in desmoplastic small round cell tumour [J].
Charles, AK ;
Moore, IE ;
Berry, PJ .
HISTOPATHOLOGY, 1997, 30 (04) :312-314
[6]   Expression of the Wilms' tumour gene WT1 in the developing human and in paediatric renal tumours: An immunohistochemical study [J].
Charles, AK ;
Mall, S ;
Watson, J ;
Berry, PJ .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 1997, 50 (03) :138-144
[7]   Ovarian serous borderline tumors with micropapillary and cribriform patterns - A study of 40 cases and comparison with 44 cases without these patterns [J].
Eichhorn, JH ;
Bell, DA ;
Young, RH ;
Scully, RE .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1999, 23 (04) :397-409
[8]   Precursor lesions of ovarian epithelial malignancy [J].
Feeley, KM ;
Wells, M .
HISTOPATHOLOGY, 2001, 38 (02) :87-95
[9]   Clear cell carcinoma of the ovary: A distinct histologic type with poor prognosis and resistance to platinum-based chemotherapy in stage III disease [J].
Goff, BA ;
delaCuesta, RS ;
Muntz, HG ;
Fleischhacker, D ;
Ek, M ;
Rice, LW ;
Nikrui, N ;
Tamimi, HK ;
Cain, JM ;
Greer, BE ;
Fuller, AF .
GYNECOLOGIC ONCOLOGY, 1996, 60 (03) :412-417
[10]  
Goldstein NS, 2002, AM J CLIN PATHOL, V117, P541