Ovarian neuroendocrine carcinomas of non-small-cell type associated with surface epithelial adenocarcinomas - A study of five cases and review of the literature

被引:57
作者
Eichhorn, JH
Lawrence, WD
Young, RH
Scully, RE
机构
[1] MASSACHUSETTS GEN HOSP,JAMES HOMER WRIGHT PATHOL LABS,BOSTON,MA 02114
[2] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
[3] HUTZEL HOSP,DEPT PATHOL,DETROIT,MI 48201
[4] INST WOMENS MED,DEPT PATHOL,DETROIT,MI
[5] WAYNE STATE UNIV,SCH MED,DEPT PATHOL,DETROIT,MI 48201
关键词
ovary; neuroendocrine carcinoma; surface epithelial carcinoma; carcinoid;
D O I
10.1097/00004347-199610000-00002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Five primary ovarian carcinomas composed of a high-grade neuroendocrine tumor of non-small-cell type acid a surface-epithelial-stromal tumor are reported. The five tumors presented in women aged 36 to 77 (mean, 57) years with abdominal distension or a palpable mass in three cases, right lower quadrant pain with tenderness and fever in one case, and a cervicovaginal smear showing a high estrogen effect in one postmenopausal patient. The tumors were unilateral, 9 to 30 (mean, 16) cm in greatest dimension, and had solid and cystic components. Three tumors were stage I; one, stage II; and one, stage III. Two patients who received chemotherapy died of tumor 8 and 36 months postoperatively, another who refused chemotherapy but later received radiation died of tumor after 19 months, a fourth was lost to follow-up, and a fifth was treated recently. Microscopically, the neuroendocrine components of all the tumors were composed predominantly of sheets, closely packed islands, cords, and trabeculae of epithelial cells with little intervening stroma. The tumor cells in the neuroendocrine areas were medium-sized to large compared with the cells of small cell carcinoma, and they contained scanty to moderate amounts of cytoplasm and hyperchromatic nuclei with coarse chromatin clumping in three cases and abundant cytoplasm and vesicular nuclei with single, large eosinophilic nucleoli in the other two, In all the cases, areas of necrosis and single-cell necrosis were extensive, and mitotic figures were abundant. Positive argyrophil and argentaffin reactions were observed in occasional to many cells in all cases. The glandular components of the tumors were grade 1/3 endometrioid adenocarcinoma (one case), grade 2/3 mucinous adenocarcinoma (2 cases), and mucinous borderline tumor with small foci of mucinous adenocarcinoma (two cases). Numerous enterochromaffin cells were identified in hematoxylin and eosin sections of the borderline mucinous components of two tumors; occasional nonargentaffin argyrophilic cells were present in the endometrioid and mucinous carcinoma components. Luteinized stromal cells were present focally in two cases, including the case in which there was evidence of a high estrogen level, Immunohistochemical studies in five cases showed staining of most cells in the solid components for cytokeratin and chromogranin A and some to most cells for serotonin and neuron-specific enolase. Neuropeptides that were detected in the solid component of one or more of the cases included vasoactive intestinal peptide, somatostatin, gastrin, and glucagon; negative results were obtained for pancreatic polypeptide and insulin. Flow cytometry in four tumors revealed that the neuroendocrine component was aneuploid in two, suspicious for aneuploidy in one, and diploid in one. Tumors of the type described are distinct pathologically from primary ovarian carcinoid tumors and small cell carcinoma of pulmonary type, Although experience with this type of tumor is limited, the prognosis appears to be poor.
引用
收藏
页码:303 / 314
页数:12
相关论文
共 45 条
  • [1] ARGYROPHIL CELLS IN BRENNER TUMORS - HISTOCHEMICAL AND IMMUNOHISTOCHEMICAL ANALYSIS
    AGUIRRE, P
    SCULLY, RE
    WOLFE, HJ
    DELELLIS, RA
    [J]. INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1986, 5 (03) : 223 - 234
  • [2] AGUIRRE P, 1986, ARCH PATHOL LAB MED, V110, P528
  • [3] MUCINOUS TUMORS OF THE OVARY WITH ARGYROPHIL CELLS - AN IMMUNOHISTOCHEMICAL ANALYSIS
    AGUIRRE, P
    DAYAL, Y
    SCULLY, RE
    DELELLIS, RA
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1984, 8 (05) : 345 - 356
  • [4] ALENGHAT E, 1986, CANCER, V58, P777, DOI 10.1002/1097-0142(19860801)58:3<777::AID-CNCR2820580327>3.0.CO
  • [5] 2-I
  • [6] PRIMARY MIXED NEUROENDOCRINE AND MUCINOUS CARCINOMA OF THE OVARY
    COLLINS, RJ
    CHEUNG, A
    NGAN, HYS
    WONG, LC
    CHAN, SYW
    MA, HK
    [J]. ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 1991, 248 (03) : 139 - 143
  • [7] CZERNOBILSKY B, 1984, CANCER, V54, P585, DOI 10.1002/1097-0142(19840801)54:3<585::AID-CNCR2820540333>3.0.CO
  • [8] 2-T
  • [9] DNA CONTENT AND PROLIFERATIVE ACTIVITY IN OVARIAN SMALL-CELL CARCINOMAS OF THE HYPERCALCEMIC TYPE - IMPLICATIONS FOR DIAGNOSIS, PROGNOSIS, AND HISTOGENESIS
    EICHHORN, JH
    BELL, DA
    YOUNG, RH
    SWYMER, CM
    FLOTTE, TJ
    PREFFER, FI
    SCULLY, RE
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1992, 98 (06) : 579 - 586
  • [10] PRIMARY OVARIAN SMALL-CELL CARCINOMA OF PULMONARY TYPE - A CLINICOPATHOLOGICAL, IMMUNOHISTOLOGIC, AND FLOW CYTOMETRIC ANALYSIS OF 11 CASES
    EICHHORN, JH
    YOUNG, RH
    SCULLY, RE
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1992, 16 (10) : 926 - 938