Department of Pathology, Université de Tours, CHU de Tours, Avenue de la République, 37170, Chambray-les-tours, France.
"Biologie des infections à polyomavirus" team, UMR INRA ISP 1282, Université de Tours, 31, Avenue Monge, 37200, Tours, France.
Mod Pathol. 2019 Apr;32(4):499-510. doi: 10.1038/s41379-018-0155-y. Epub 2018 Oct 22.
Merkel cell carcinoma is a rare neuroendocrine carcinoma of the skin mostly induced by Merkel cell polyomavirus integration. Cytokeratin 20 (CK20) positivity is currently used to distinguish Merkel cell carcinomas from other neuroendocrine carcinomas. However, this distinction may be challenging in CK20-negative cases and in cases without a primary skin tumor. The objectives of this study were first to evaluate the diagnostic accuracy of previously described markers for the diagnosis of Merkel cell carcinoma and second to validate these markers in the setting of difficult-to-diagnose Merkel cell carcinoma variants. In a preliminary set (n = 30), we assessed optimal immunohistochemical patterns (CK20, thyroid transcription factor 1 [TTF-1], atonal homolog 1 [ATOH1], neurofilament [NF], special AT-rich sequence-binding protein 2 [SATB2], paired box protein 5, terminal desoxynucleotidyl transferase, CD99, mucin 1, and Merkel cell polyomavirus-large T antigen) and Merkel cell polyomavirus load thresholds (real-time PCR). The diagnostic accuracy of each marker was then assessed in a validation set of 103 Merkel cell carcinomas (9 CK20-negative cases and 15 cases without a primary skin tumor) and 70 extracutaneous neuroendocrine carcinoma cases. The most discriminant markers for a diagnosis of Merkel cell carcinoma were SATB2, NF expression, and Merkel cell polyomavirus DNA detection (positive likelihood ratios: 36.6, 44.4, and 28.2, respectively). Regarding Merkel cell carcinoma variants, cases without a primary skin tumor retained a similar immunohistochemical profile and CK20-negative tumors displayed a different profile (decrease frequency of NF and SATB2 expression), but Merkel cell polyomavirus DNA remained detected (78% of cases by qPCR). Moreover, 8/9 (89%) CK20-negative Merkel cell carcinoma cases but only 3/61 (5%) CK20-negative extracutaneous neuroendocrine cases were positive for at least one of these markers. In conclusion, detection of SATB2 and NF expression and Merkel cell polyomavirus DNA helps distinguish between Merkel cell carcinoma classical and variant cases and extracutaneous neuroendocrine carcinomas.
默克尔细胞癌是一种罕见的皮肤神经内分泌癌,主要由默克尔细胞多瘤病毒整合引起。细胞角蛋白 20(CK20)阳性目前用于将默克尔细胞癌与其他神经内分泌癌区分开来。然而,在 CK20 阴性病例和无原发性皮肤肿瘤的病例中,这种区分可能具有挑战性。本研究的目的首先是评估先前描述的用于诊断默克尔细胞癌的标记物的诊断准确性,其次是在难以诊断的默克尔细胞癌变体中验证这些标记物。在初步组(n=30)中,我们评估了最佳的免疫组织化学模式(CK20、甲状腺转录因子 1 [TTF-1]、同源异型盒 1 [ATOH1]、神经丝 [NF]、特殊富含 AT 的序列结合蛋白 2 [SATB2]、配对盒蛋白 5、末端脱氧核苷酸转移酶、CD99、粘蛋白 1 和默克尔细胞多瘤病毒大 T 抗原)和默克尔细胞多瘤病毒载量阈值(实时 PCR)。然后,在 103 例默克尔细胞癌(9 例 CK20 阴性病例和 15 例无原发性皮肤肿瘤病例)和 70 例皮肤外神经内分泌癌病例的验证组中评估每个标记物的诊断准确性。用于诊断默克尔细胞癌的最具鉴别力的标记物是 SATB2、NF 表达和默克尔细胞多瘤病毒 DNA 检测(阳性似然比:分别为 36.6、44.4 和 28.2)。对于默克尔细胞癌变体,无原发性皮肤肿瘤的病例保留了相似的免疫组织化学特征,而 CK20 阴性肿瘤显示出不同的特征(NF 和 SATB2 表达频率降低),但仍可检测到默克尔细胞多瘤病毒 DNA(78%的病例通过 qPCR)。此外,8/9(89%)CK20 阴性默克尔细胞癌病例但仅 3/61(5%)CK20 阴性皮肤外神经内分泌癌病例为至少一种这些标记物阳性。总之,检测 SATB2 和 NF 表达以及默克尔细胞多瘤病毒 DNA 有助于区分默克尔细胞癌经典和变体病例与皮肤外神经内分泌癌。