期刊文献+

超常胎盘部位的病理形态与免疫组化研究 被引量:3

Pathological and immunohistochemical study of exaggerated placental site
下载PDF
导出
摘要 目的:探讨超常胎盘部位(EPS) 的病理形态与免疫组化特征,提出鉴别诊断要点。方法:对17 例经病理检查诊断为EPS的病例进行病理学形态观察,采用免疫组化方法标记滋养细胞HCG、HPL、EMA、PRL、PLAP、Vim 、actin、cerbB2 和cmyc。结果:EPS组织学特征为以中间型为主的滋养细胞向蜕膜及平滑肌浸润,不破坏原有组织结构,并保留部分胎盘床特点。免疫组化标记HPL、EMA呈阳性或强阳性,HCG多为弱阳性,其他多为阴性。结论:EPS属于中间型滋养细胞为主的妊娠滋养细胞疾病。鉴别诊断应结合组织学、免疫组化及临床表现综合判断。 Purpose To study the pathological features and immunohistochemical expressions of exaggerated placental site (EPS) and to propose its differential diagnosis. Methods The pathological features of EPS were observed in 17 cases, and the expressions of HCG, HPL, EMA, PRL, PLAP, Vim, actin, c erbB 2 and c myc were analyzed immunohistochemically. Results The histological features of EPS were that trophoblasts, mainly intermediate trophoblast (IT), infiltrated into decidua and myometrium layers, while original histological features were not destroyed, and placental site features were remained partially. The expressions of HPL and EMA were positive or strongly positive in all cases, HCG weakly positive in the most cases. Conclusion EPS is a lesion of gestational trophoblastic disease primarily involving IT. Its differential diagnosis depends on combining histological characteristics, immunohistochemical findings and clinical features.
出处 《临床与实验病理学杂志》 CAS CSCD 1999年第5期387-389,I057,共4页 Chinese Journal of Clinical and Experimental Pathology
关键词 胎盘疾病 滋养层 病理学 免疫组织化学 EPS placenta disease trophoblast pathology immunohistochemistry
  • 相关文献

参考文献2

共引文献24

同被引文献20

  • 1Szony BJ, Hegedus K, Bata Z, et al. Cytotrophoblast cells from human first-trimester placental villi: isolation, characterization, cuhivation and research applications. Orv Hetil,2002,143(35) :2047-2054.
  • 2Potgens AJG, Gaus G, Frank HG, et al. Characterization of trophoblast cell isolation by a modified flow cytometry assay. Placenta, 2001,22:251-255.
  • 3E1-Hashash AH, Kimber SJ. Trophoblast differentiation in vitro: establishment and characterization of a serum-free culture model for murine secondary trophoblast giant cells. Reproduction,2004,128( 1 ) :53 - 71.
  • 4King A, Thomas L, Bischof P. Cell Culture Models of Trophoblast 11 : Trephoblast Cell Lines A Workshop Report.Placenta,2000,14:113-119.
  • 5Graham CH, Hawley TS, Hawley RG, et al. Establishment and characterizafion of first trime,ter human trophoblast cells with extended lifespan. Experi Cell Res, 1993,206:204.
  • 6Khoo NKS,Bechberger JF,Shepherd T,et aI.SV40 Tag transformation of the normal invasive trophoblast results in a pre malignant phenotype. Machanis ms responsible for hyperinvasiveness and resistance to anti-invasive action of TGFβ. Int J Cancer, 1998,77:429.
  • 7Frank H G, Morrish DW. Cell cuhure models of human trophohalst primary culture of trophoblast-a workshop report Placenta, 2001, (SupplA): 104-106.
  • 8Henson MC,Shi W, Greene SJ,et al. Effocts of pregnant human, nonpregnant human, and fetal bovine sera on human chofionic gonadotropin, estradiol, and progesterone release by cultured human trophoblast cells. Endocrinology,1996,137(5) :2067 - 2074.
  • 9Hanna J, Wald O, Goldman Wohl D, et al. CXCL 12 expression by invasive trophoblasts induces the specific migration of CD 16 negative human natural killer cells. Blood, 2003,102:1569 - 1577.
  • 10El Hashash HA,Kimber SJ.Trophoblast differentiation in vitro:establishment and characterization of a serum-free culture model for murine secondary trophoblast giant cells[J].Reproduction,2004,128(1):53-71.

引证文献3

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部