Stewart Colin J R, Crook Maxine L
Department of Histopathology (C.J.R.S., M.L.C.), King Edward Memorial Hospital, Subiaco, Perth School for Women's and Infants' Health (C.J.R.S.), University of Western Australia, WA, Australia.
Int J Gynecol Pathol. 2015 Jan;34(1):90-100. doi: 10.1097/PGP.0000000000000107.
Microglandular hyperplasia (MGH) is a common endocervical alteration that in most cases presents no diagnostic difficulty. However, MGH rarely shows atypical features that may mimic endocervical neoplasia, while conversely endometrial carcinomas can show deceptively bland MGH-like appearances. It has been suggested that immunohistochemical analysis is useful in this context, but relatively few studies have specifically investigated microglandular pattern lesions and the results have been conflicting. In this study, we have examined a series of MGH (n=24), atypical MGH (n=2), and endometrial microglandular-like carcinomas (EMC, n=8), with a panel of antibodies including PAX2, cyclin D1, p16, vimentin, and Ki67. Loss of PAX2 staining was identified only in EMC but had relatively poor sensitivity for a malignant diagnosis (3/8 cases). Seven EMCs showed p16 expression and staining was diffuse (≥50% cells) in 6 cases, whereas all conventional MGH lesions were negative. However, 1 case of atypical MGH was also p16-positive. Cyclin D1, vimentin, and Ki67 did not reliably distinguish the benign and malignant microglandular lesions because of considerable overlap in staining patterns. In summary, none of the antibodies examined proved completely sensitive and specific, but a p16-positive/PAX2-negative phenotype favored a diagnosis of EMC. Pathologists should be aware that EMC, like some other types of endometrial carcinoma, are commonly p16-positive to avoid misinterpretation as a primary endocervical neoplasm. In practice, correlation of the histologic, immunohistologic, and clinical findings is necessary for accurate interpretation of microgandular-pattern lesions, particularly in small biopsy samples.
微腺性增生(MGH)是一种常见的宫颈内膜改变,多数情况下诊断并不困难。然而,MGH很少表现出可能模仿宫颈内膜肿瘤的非典型特征,相反,子宫内膜癌可呈现出看似良性的MGH样表现。有人提出免疫组化分析在此情况下有用,但相对较少的研究专门调查微腺性模式病变,且结果相互矛盾。在本研究中,我们用一组抗体,包括PAX2、细胞周期蛋白D1、p16、波形蛋白和Ki67,检测了一系列MGH(n = 24)、非典型MGH(n = 2)和子宫内膜微腺性样癌(EMC,n = 8)。仅在EMC中发现PAX2染色缺失,但对恶性诊断的敏感性相对较差(3/8例)。7例EMC显示p16表达,6例染色弥漫(≥50%细胞),而所有传统MGH病变均为阴性。然而,1例非典型MGH也为p16阳性。细胞周期蛋白D1、波形蛋白和Ki67由于染色模式有相当大的重叠,不能可靠地区分良性和恶性微腺性病变。总之,所检测的抗体均未证明完全敏感和特异,但p16阳性/PAX2阴性表型有利于EMC的诊断。病理学家应意识到,EMC与其他一些类型的子宫内膜癌一样,通常p16阳性,以避免误诊为原发性宫颈内膜肿瘤。在实践中,组织学、免疫组织学和临床发现的相关性对于准确解释微腺性模式病变是必要的,特别是在小活检样本中。