Suppr超能文献

阴道腺病的宫颈内膜型(作者译)

[Endocervical form of the vaginal adenosis (author's transl)].

作者信息

Walz K A, Metzger H, Ludwig H

出版信息

Arch Gynakol. 1978 Oct 18;225(4):293-303. doi: 10.1007/BF02570573.

Abstract

Vaginal adenosis is a rare kind of disease without specific symptoms and does not represent a very serious disorder from the beginning. Concerning the etiology teratogenetic dependencies are known which still are interpreted in different ways in the recent literature. The increased number of cases, including those with clear-cell-carcinoma of the vagina, in juveniles after exposition to DES during the early embryonal development shows in particular (Central index for the stilbestrol-adenosis-carcinoma-syndrome in the USA, since 1971) a wrong pathway in the organogenesis of cervix and vagina. This occurs at the interference zone between the epithelium of the Müllerian ducts and the epithelium of the sinus urogenitalis of the female fetus and in so far constitutes the origin of vaginal adenosis. The basics of the possibility of the development of such irregular differentiation and heterotopic dissemination are proven again by the case report of a vaginal adenosis showing the highly differentiated endocervical type. Not every case of vaginal adenosis does signify a precancerous lesion. The separation of the most frequently endocervical manifestation observed from endometrial and intermediate forms might be difficult. A positive distinction is prognostically essential, however, since clear-cell-carcinomas of the vagina are known in occurence with the endometrial type of vaginal adenosis only. Scanning electron microscopy as a method to follow tissue organization reveals the way of differentiation between the various types via ultrastructural analysis for vaginal adenosis is an example for failures of developmental organization. The same analysis is feasible in cytological smears also. The therapeutic requirements of vaginal adenosis depend on the tissular differentiation and the given local extent of the adenomatous lesions.

摘要

阴道腺病是一种罕见疾病,无特定症状,起初并非非常严重的病症。关于其病因,已知存在致畸依赖性,近期文献对此仍有不同解读。自1971年以来,美国青少年在胚胎发育早期接触己烯雌酚后,包括阴道透明细胞癌在内的病例数量增加,这尤其显示出宫颈和阴道器官发生过程中的错误路径。这种情况发生在女性胎儿苗勒管上皮与泌尿生殖窦上皮的交界区域,就此构成了阴道腺病的起源。一例显示高度分化宫颈内膜型的阴道腺病病例报告再次证明了这种不规则分化和异位播散发生的可能性。并非每例阴道腺病都意味着癌前病变。区分最常见的宫颈内膜表现与子宫内膜型及中间型可能存在困难。然而,明确区分在预后方面至关重要,因为已知阴道透明细胞癌仅与子宫内膜型阴道腺病相关。扫描电子显微镜作为一种观察组织结构的方法,通过超微结构分析揭示了阴道腺病不同类型之间的分化方式,这是发育组织异常的一个例子。同样的分析在细胞学涂片检查中也可行。阴道腺病的治疗需求取决于组织分化情况以及腺瘤性病变的局部范围。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验