Department of Pathology, University of Medicine and Pharmacy of Targu Mures, Targu Mures.
Vancouver General Hospital, Vancouver, BC, Canada.
Am J Surg Pathol. 2018 Aug;42(8):989-1000. doi: 10.1097/PAS.0000000000001090.
The International Endocervical Adenocarcinoma Criteria and Classification was developed to separate endocervical adenocarcinomas (ECAs) into 2 main categories on the basis of morphology such as human papilloma virus-associated (HPVA) and non-human papilloma virus-associated adenocarcinomas. We aimed to improve the diagnostic accuracy of International Endocervical Adenocarcinoma Criteria and Classification by performing a comprehensive immunohistochemical evaluation and constructing objective immunohistochemical-based algorithms for the classification of these tumors. Tissue microarrays were constructed from 297 of 409 cases used to develop the original classification. Immunostains included p16, p53, estrogen receptor (ER), progesterone receptor, androgen receptor, Vimentin, CK7, CK20, HER2, HIK1083, MUC6, CA-IX, SATB2, HNF-1beta, napsin A, PAX8, CDX2, GATA3, p63, p40, and TTF-1. High-risk human papilloma virus (HR-HPV) was detected by in situ hybridization (ISH) using probes against E6 and E7 mRNA expressed in 18 different virus types. Vimentin, ER, and progesterone receptor were expressed in a significant minority of ECAs, mostly HPVAs, limiting their use in differential diagnosis of endometrioid carcinoma when unaccompanied by HPV-ISH or p16. HR-HPV ISH had superior sensitivity, specificity, and negative and positive predictive values compared with p16, as published previously. HNF-1beta did not have the anticipated discriminatory power for clear cell carcinoma, nor did MUC6 or CA-IX for gastric-type carcinoma. HNF-1beta and napsin A were variably expressed in clear cell carcinoma, with HNF-1beta demonstrating less specificity, as it was ubiquitously expressed in gastric-type carcinoma and in the majority of HPV-associated mucinous (predominantly intestinal-type and invasive ECA resembling stratified mucin-producing intraepithelial lesion [iSMILE]) and usual-type carcinomas. HIK1083 was expressed in nearly half of gastric-type carcinomas, but not in the vast majority of other subtypes. GATA3 was positive in 10% of usual-type adenocarcinomas and in single examples of other subtypes. Rare gastric-type and HPVA mucinous carcinomas displayed HER2 overexpression. Androgen receptor was positive in 6% of usual-type adenocarcinomas. Aberrant p53 expression was found in only 3.6% of usual-type HPVA carcinomas, but it was more prevalent in mucinous (intestinal type and iSMILE) HPVAs and non-human papilloma virus-associates (particularly in gastric-type carcinoma, >50% of cases). The following diagnostic classification algorithms were developed with the above data. Carcinomas without overt cytoplasmic mucin (endometrioid, usual-type endocervical, clear cell, and mesonephric carcinomas) can be subclassified using HR-HPV ISH, ER, and GATA3, whereas carcinomas with easily appreciated cytoplasmic mucin (endometrioid carcinoma with mucinous features, HPVA mucinous, and gastric-type carcinomas) can be subclassified with HR-HPV ISH and ER.
国际宫颈内膜腺癌分类标准旨在基于形态学将宫颈内膜腺癌(ECAs)分为 2 个主要类别,例如人乳头瘤病毒相关(HPVA)和非人乳头瘤病毒相关腺癌。我们旨在通过进行全面的免疫组织化学评估并构建这些肿瘤分类的客观免疫组织化学算法来提高国际宫颈内膜腺癌分类标准的诊断准确性。使用构建原始分类的 409 例病例中的 297 例构建了组织微阵列。免疫染色包括 p16、p53、雌激素受体(ER)、孕激素受体、雄激素受体、波形蛋白、CK7、CK20、HER2、HIK1083、MUC6、CA-IX、SATB2、HNF-1β、napsin A、PAX8、CDX2、GATA3、p63、p40 和 TTF-1。使用针对在 18 种不同病毒类型中表达的 E6 和 E7 mRNA 的原位杂交(ISH)检测高危型人乳头瘤病毒(HR-HPV)。波形蛋白、ER 和孕激素受体在大多数 HPVAs 中的表达比例较低,限制了它们在 HPV-ISH 或 p16 未伴随时在子宫内膜样癌的鉴别诊断中的使用。HR-HPV ISH 的敏感性、特异性、阴性和阳性预测值均优于 p16,这在之前已经发表过。HNF-1β 对透明细胞癌没有预期的鉴别能力,MUC6 或 CA-IX 对胃型癌也没有。HNF-1β 和 napsin A 在透明细胞癌中表达不同,HNF-1β 的特异性较低,因为它在胃型癌和大多数 HPV 相关的黏液性(主要为肠型和侵袭性 ECA 类似于分层黏液产生上皮内病变 [iSMILE])和普通型癌中广泛表达。HIK1083 在近一半的胃型癌中表达,但在大多数其他亚型中并不表达。GATA3 在 10%的普通型腺癌和其他少数亚型中呈阳性。罕见的胃型和 HPVA 黏液腺癌显示 HER2 过度表达。雄激素受体在 6%的普通型腺癌中呈阳性。仅在 3.6%的普通型 HPVA 黏液腺癌中发现异常 p53 表达,但在黏液性(肠型和 iSMILE)HPVAs 和非 HPV 相关癌(特别是胃型癌,>50%的病例)中更为常见。使用上述数据开发了以下诊断分类算法。没有明显细胞质黏液的癌(子宫内膜样癌、普通型宫颈内膜、透明细胞癌和中肾管癌)可以使用 HR-HPV ISH、ER 和 GATA3 进行亚分类,而具有易于识别的细胞质黏液的癌(具有黏液特征的子宫内膜样癌、HPVA 黏液性癌和胃型癌)可以使用 HR-HPV ISH 和 ER 进行亚分类。