Song Liling, Zhu Ning, Jiang Lei, Gao Dong, Yu Guohua
The Second School of Clinical Medicine of Binzhou Medical University, Yantai, Shandong, China.
Department of Pathology, Yantai Yuhuangding Hospital, The Affiliated Hospital of Qingdao University, Yantai, China.
Front Oncol. 2025 Sep 3;15:1530871. doi: 10.3389/fonc.2025.1530871. eCollection 2025.
Primary cutaneous mucinous carcinoma (PCMC) is a rare malignant neoplasm, with approximately 450 cases reported worldwide to date. Its histological features closely resemble those of mucinous carcinoma of the breast, posing significant diagnostic challenges. We report a case of PCMC occurring at the upper margin of the eyelid in a 65-year-old male who presented with a painless, progressively enlarging mass over a four-year period. Histopathological examination following surgical excision confirmed the diagnosis of PCMC, with immunohistochemical staining demonstrating co-expression of TRPS1 and GATA3. This case highlights several key clinical and pathological characteristics of PCMC. The tumor typically affects middle-aged to elderly males and demonstrates low metastatic potential but a high rate of local recurrence. Histologically, it is difficult to distinguish from cutaneous metastatic mucinous carcinoma (MMC), particularly of breast origin. In this context, the co-expression of TRPS1 and GATA3 necessitates careful interpretation, as these markers are not exclusive to PCMC. The diagnostic utility of TRPS1 lies not in its individual specificity, but rather in its combined use with other markers such as GATA3. Radical surgical excision remains the mainstay of treatment, with adjuvant endocrine therapy considered in ER/PR-positive cases. Compared to cutaneous MMC, PCMC generally carries a more favorable prognosis, reinforcing the importance of early and accurate diagnosis. Ultimately, the diagnosis of PCMC relies on a comprehensive evaluation that integrates clinical presentation, imaging findings, histological architecture, and immunohistochemical profiles.
原发性皮肤黏液癌(PCMC)是一种罕见的恶性肿瘤,迄今为止全球报道的病例约有450例。其组织学特征与乳腺黏液癌极为相似,给诊断带来了巨大挑战。我们报告一例发生在一名65岁男性眼睑上缘的PCMC病例,该患者在四年间出现了一个无痛性、逐渐增大的肿块。手术切除后的组织病理学检查确诊为PCMC,免疫组化染色显示TRPS1和GATA3共表达。该病例凸显了PCMC的几个关键临床和病理特征。该肿瘤通常累及中老年男性,转移潜能低,但局部复发率高。在组织学上,很难将其与皮肤转移性黏液癌(MMC)区分开来,尤其是乳腺来源的MMC。在这种情况下,TRPS1和GATA3的共表达需要仔细解读,因为这些标志物并非PCMC所特有。TRPS1的诊断价值不在于其单独的特异性,而在于它与其他标志物如GATA3联合使用。根治性手术切除仍然是主要的治疗方法,雌激素受体/孕激素受体(ER/PR)阳性的病例可考虑辅助内分泌治疗。与皮肤MMC相比,PCMC通常预后较好,这凸显了早期准确诊断的重要性。最终,PCMC的诊断依赖于综合评估,包括临床表现、影像学检查结果、组织结构和免疫组化特征。