Findeis Sarah K, Readinger Allison, Mitchell James, Agarwal Atin
Department of Pathology, Baylor University Medical CenterDallasTexas.
Department of Pathology, UT Southwestern Medical CenterDallasTexas.
Proc (Bayl Univ Med Cent). 2020 Apr 21;33(3):424-426. doi: 10.1080/08998280.2020.1747342. eCollection 2020 Jul.
Cutaneous signet-ring cell squamous cell carcinoma (SRCSCC) is a rare variant, most commonly occurring in the head and neck. We report a case of a 66-year-old transgender woman with an ulcerated growing facial mass measuring 5.6 × 4.0 × 2.0 cm. Histological analysis showed features consistent with SRCSCC. Immunohistochemical analysis showed positive staining for high-molecular-weight cytokeratin, estrogen receptor (1-2+ in 10%), E-cadherin (mostly positive with partial loss), and p40 and negative staining for Ber EP-4, cytokeratin 7, low-molecular-weight cytokeratin, mucicarmine, Alcian blue PAS, HER2, and MUC4. The tumor had invaded the perineurium, lymphovascular spaces, and subcutaneum. Additionally, microsatellite instability testing was negative. This case adds to the limited knowledge of this poorly characterized entity.
皮肤印戒细胞鳞状细胞癌(SRCSCC)是一种罕见的变体,最常发生于头颈部。我们报告一例66岁的变性女性病例,其面部有一个生长性溃疡肿物,大小为5.6×4.0×2.0厘米。组织学分析显示其特征符合SRCSCC。免疫组化分析显示高分子量细胞角蛋白、雌激素受体(10%为1-2+)、E-钙黏蛋白(大多为阳性,部分缺失)和p40呈阳性染色,而Ber EP-4、细胞角蛋白7、低分子量细胞角蛋白、黏液卡红、阿尔辛蓝过碘酸雪夫反应、HER2和MUC4呈阴性染色。肿瘤已侵犯神经束膜、淋巴管间隙和皮下组织。此外,微卫星不稳定性检测为阴性。该病例增加了对这种特征不明的实体的有限认知。