Terada Tadashi
Department of Pathology, Shizuoka City Shimizu Hospital, Shimizu, Shizuoka, Japan.
Int J Clin Exp Pathol. 2013 May 15;6(6):1164-8. Print 2013.
Primary cutaneous small cell carcinoma (PC-SmCC) is extremely rare; only two cases have been reported in the world literatures. A 79-year-old woman presented a small cutaneous tumor in the face. Physical examination showed a tumor measuring 1.0x.08x0.6 cm in the shallow skin of the face. Excisional skin biopsy was performed. The biopsy showed complete excision of the tumor. The tumor was located in the shallow dermis and no connections to epidermis were seen. The tumor was invasive into subcutaneous tissue and surrounding dermis. The tumor was very hypercellular tumor composed of small cells with scant cytoplasm, hyperchromatic nu lei, negative nucleoli, and molded nuclei. The shapes of tumor cells are round, ovoid or spindle. The histological appearances fulfilled the criteria of SmCC of WHO. Immunohistochemically, the tumor cells were positive for cytokeratin (CK) AE1/3, CK CAM5.2, CK34BE12, CD5, CD6, CK8, p63, NSE, NCAM, synaptophysin (focal), chromogranin (focal), p53, KIT, PDGFRA and Ki-67 (labeling index (LI)=86%). They were negative for CK7, CK19, CK20, EMA, vimentin, CEA, S100 protein, CA19-9, TTF-1, MUC1, MUC2, MUC5AC and MUC6. Mucin histochemistry revealed no mucins. A molecular genetic analysis of PCR-direct sequencing identified no mutations of KIT (exons 9, 11, 13, and 17) and PDGFRA (exons 12 and 18) genes. The author diagnosed this cutaneous tumor as SmCC. Post-diagnosis whole body examination using various imaging and endoscopic techniques revealed no tumors. This may confirm that the skin tumor was primary. The cutaneous tumor was completely resected with wide margins. The patient is now followed up without therapy 8 months after the diagnosis. No recurrence or metastasis is seen. The differential diagnosis from Merkel cell carcinoma and basal cell carcinoma is very difficult and herein discussed.
原发性皮肤小细胞癌(PC-SmCC)极为罕见;世界文献中仅报道过两例。一名79岁女性面部出现一个小的皮肤肿瘤。体格检查显示面部浅表皮下有一个大小为1.0×0.8×0.6 cm的肿瘤。进行了切除性皮肤活检。活检显示肿瘤完整切除。肿瘤位于真皮浅层,未见与表皮相连。肿瘤侵犯皮下组织和周围真皮。肿瘤是一个细胞高度密集的肿瘤,由细胞质稀少、核染色质深、无核仁且核呈镶嵌状的小细胞组成。肿瘤细胞形状为圆形、卵圆形或梭形。组织学表现符合世界卫生组织小细胞癌的标准。免疫组化检查显示,肿瘤细胞细胞角蛋白(CK)AE1/3、CK CAM5.2、CK34BE12、CD5、CD6、CK8、p63、NSE、NCAM、突触素(局灶性)、嗜铬粒蛋白(局灶性)、p53、KIT、血小板衍生生长因子受体A(PDGFRA)和Ki-67(标记指数(LI)=86%)呈阳性。它们CK7、CK19、CK20、上皮膜抗原(EMA)、波形蛋白、癌胚抗原(CEA)、S100蛋白、CA19-9、甲状腺转录因子-1(TTF-1)、黏蛋白1(MUC1)、黏蛋白2(MUC2)、黏蛋白5AC和黏蛋白6呈阴性。黏液组织化学检查未发现黏液。聚合酶链反应直接测序的分子遗传学分析未发现KIT基因(第9、11、13和17外显子)和PDGFRA基因(第12和18外显子)的突变。作者将该皮肤肿瘤诊断为小细胞癌。诊断后使用各种影像学和内镜技术进行的全身检查未发现肿瘤。这可能证实该皮肤肿瘤是原发性的。皮肤肿瘤已广泛切除边缘组织。患者在诊断后8个月未经治疗进行随访。未见复发或转移。文中讨论了与默克尔细胞癌和基底细胞癌的鉴别诊断非常困难。