TUMOR-MARKERS OF EPITHELIAL OVARIAN NEOPLASMS

被引:13
作者
KHALIFA, MA
SESTERHENN, IA
机构
[1] ARMED FORCES INST PATHOL,DEPT GENITOURINARY PATHOL,WASHINGTON,DC 20306
[2] ARMED FORCES INST PATHOL,DEPT GYNECOL & BREAST PATHOL,WASHINGTON,DC 20306
关键词
Carbohydrate histochemistry; Lectin histochemistry; Ovarian tumors; Tumor markers; Tumors of low malignant potential;
D O I
10.1097/00004347-199007000-00003
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Ninety-three formalin-fixed, paraffin-embedded surgical specimens from 69 ovarian tumors representing all five epithelial cell types were studied by immunohistochemistry, peanut and ulex lectin binding, and carbohydrate histochemistry. Carcinoembryonic antigen (CEA) was mostly noticeable in mucinous tumors (21 of 26). Glycogen was highly prevalent in clear cell (8 of 9) and endometrioid (4 of 6) carcinomas, in contrast to serous carcinomas (3 of 6), where it was only focally distributed, and was completely absent in all mucinous tumors. Among the different types of malignant tumors examined, mucinous carcinomas most frequently contained neutral mucins (6 of 8). In mucinous tumors, an increase in CEA content and a decrease in the total mucin secretion, particularly the strongly acidic sulfated group, were found to parallel the increased malignant potential of the tumor. Peanut and/or ulex lectin binding was a feature common to almost all epithelial neoplasms. Although peanut lectin showed a slightly higher affinity to serous and clear cell tumors, while ulex lectin was bound more to mucinous and endometrioid neoplasms, distribution of d-galactose and l-fucose does not have a diagnostic utility in these tumors. Placental lactogen was detected in 3 of 17 benign tumors and one of 19 tumors of low malignant potential (LMP). The β subunit of hCG was found in one of 17 benign tumors, in 2 of 19 LMP tumors, and in 3 of 31 carcinomas. © 1990 International Society of Gynecological Pathologists.
引用
收藏
页码:217 / 230
页数:14
相关论文
共 25 条
[1]   USE OF IMMUNOHISTOCHEMICAL STAINING PANEL FOR CHARACTERIZATION OF OVARIAN NEOPLASMS [J].
ASHORN, P ;
HELLE, M ;
HELIN, H ;
ASHORN, R ;
KROHN, K .
JOURNAL OF CLINICAL PATHOLOGY, 1988, 41 (01) :12-16
[2]  
BHATTACHARYA M, 1973, CANCER-AM CANCER SOC, V31, P588, DOI 10.1002/1097-0142(197303)31:3<588::AID-CNCR2820310314>3.0.CO
[3]  
2-E
[4]   IMMUNOLOGICAL COMPARISON BETWEEN SEROUS CYSTADENOCARCINOMA OF OVARY AND OTHER HUMAN GYNECOLOGIC TUMORS [J].
BHATTACHARYA, M ;
BARLOW, JJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1973, 117 (06) :849-853
[5]  
BLAUSTEIN A, 1982, CANCER, V49, P722, DOI 10.1002/1097-0142(19820215)49:4<722::AID-CNCR2820490421>3.0.CO
[6]  
2-C
[7]   ECTOPIC PRODUCTION OF HUMAN CHORIONIC GONADOTROPIN BY NEOPLASMS [J].
BRAUNSTEIN, GD ;
VAITUKAITIS, JL ;
CARBONE, PP ;
ROSS, GT .
ANNALS OF INTERNAL MEDICINE, 1973, 78 (01) :39-45
[8]   HISTOCHEMICAL-STUDY OF LECTIN BINDING TO GESTATIONAL ENDOMETRIUM [J].
BYCHKOV, V ;
TOTO, PD .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1987, 6 (01) :66-72
[9]   LECTIN BINDING TO NORMAL HUMAN-ENDOMETRIUM [J].
BYCHKOV, V ;
TOTO, PD .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 1986, 22 (01) :29-33
[10]  
CROWTHER ME, 1979, OBSTET GYNECOL, V53, P59