Hoang Lien N, Park Kay J, Soslow Robert A, Murali Rajmohan
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Marie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Pathology. 2016 Jun;48(4):291-302. doi: 10.1016/j.pathol.2016.02.015. Epub 2016 Apr 23.
Growing evidence has established two major types of vulvar intraepithelial neoplasia (VIN), which correspond to two distinct oncogenic pathways to vulvar squamous cell carcinoma (VSCC). While the incidence of VSCC has remained relatively stable over the last three decades, the incidence of VIN has increased. VIN of usual type (uVIN) is human papillomavirus (HPV)-driven, affects younger women and is a multicentric disease. In contrast, VIN of differentiated type (dVIN) occurs in post-menopausal women and develops independent of HPV infection. dVIN often arises in a background of lichen sclerosus and chronic inflammatory dermatoses. Although isolated dVIN is significantly less common than uVIN, dVIN bears a greater risk for malignant transformation to VSCC and progresses over a shorter time interval. On histological examination, uVIN displays conspicuous architectural and cytological abnormalities, while the morphological features that characterise dVIN are much more subtle and raise a wide differential diagnosis. On the molecular level, dVIN is characterised by a higher number of somatic mutations, particularly in TP53. Here we review the classification, epidemiology, clinical features, histomorphology, ancillary markers and molecular genetics of both types of VIN, and discuss the morphological challenges faced by pathologists in interpreting these lesions.
越来越多的证据表明,外阴上皮内瘤变(VIN)主要有两种类型,它们分别对应外阴鳞状细胞癌(VSCC)的两种不同致癌途径。在过去三十年中,虽然VSCC的发病率一直相对稳定,但VIN的发病率却有所上升。寻常型VIN(uVIN)由人乳头瘤病毒(HPV)驱动,影响年轻女性,是一种多中心疾病。相比之下,分化型VIN(dVIN)发生在绝经后女性中,其发展独立于HPV感染。dVIN通常发生在硬化性苔藓和慢性炎症性皮肤病的背景下。虽然孤立的dVIN比uVIN明显少见,但dVIN发生恶性转化为VSCC的风险更大,且在更短的时间间隔内进展。在组织学检查中,uVIN表现出明显的结构和细胞学异常,而dVIN的形态学特征则更为细微,需要进行广泛的鉴别诊断。在分子水平上,dVIN的特征是体细胞突变数量较多,尤其是在TP53基因中。在此,我们综述了两种类型VIN的分类、流行病学、临床特征、组织形态学、辅助标志物和分子遗传学,并讨论了病理学家在解读这些病变时面临的形态学挑战。