Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
Semin Diagn Pathol. 2010 Nov;27(4):215-25. doi: 10.1053/j.semdp.2010.09.007.
Endometrial intraepithelial neoplasia (EIN) is a monoclonal premalignant endometrial glandular lesion that precedes the development of endometrioid-type endometrial adenocarcinoma. EIN arises through complex interactions involving the sequential accumulation of genetic damage in endometrial glands and the positive selective pressure of unopposed estrogen. Recent data have revealed a preclinical latent precursor lesion composed of mutated but morphologically nondescript glands that may persist for years in normal-appearing premenopausal cycling endometrium. This latent precursor shares many of the molecular features of EIN and endometrial adenocarcinoma, including frequent inactivation of both the tumor suppressor gene PTEN and the paired box-containing gene PAX2. Upon progression to EIN, the distinctive appearance of crowded and cytologically altered glands heralds a 45-fold increased risk of developing endometrial adenocarcinoma. To preserve the high predictability of EIN for concurrent/ subsequent adenocarcinoma, strict adherence to defined diagnostic criteria is essential. These criteria, as well as potential diagnostic pitfalls and their resolution, are discussed herein.
子宫内膜上皮内瘤变(EIN)是一种单克隆癌前子宫内膜腺性病变,发生于子宫内膜样型子宫内膜腺癌之前。EIN 通过涉及子宫内膜腺体中遗传损伤的顺序积累以及雌激素无拮抗的阳性选择压力的复杂相互作用而发生。最近的数据显示,存在一种临床前潜伏前体病变,由突变但形态上无明显特征的腺体组成,这些腺体可能在绝经前正常周期的子宫内膜中持续存在多年。这种潜伏前体与 EIN 和子宫内膜腺癌具有许多共同的分子特征,包括肿瘤抑制基因 PTEN 和配对盒基因 PAX2 的频繁失活。进展为 EIN 时,拥挤和细胞学改变的腺体的独特外观预示着发生子宫内膜腺癌的风险增加 45 倍。为了保持 EIN 对同时/随后发生的腺癌的高预测性,严格遵循明确的诊断标准至关重要。本文讨论了这些标准以及潜在的诊断陷阱及其解决方法。