Pai S A, Naresh K N, Masih K, Ramarao C, Borges A M
Department of Pathology, Tata Memorial Hospital, Mumbai (Bombay), India.
Hum Pathol. 1998 Jul;29(7):718-22. doi: 10.1016/s0046-8177(98)90281-7.
We report four cases of sinonasal teratocarcinosarcoma (SNTCS), a rare malignant tumor that displays combined features of an immature or malignant teratoma and a carcinosarcoma. The patients, three men and one woman, were all adults ranging in age from 21 to 69 years who presented with nasal obstruction and epistaxis. The tumors were typically composed of round cells and short spindle cells with neuroectodermal/rosette-like structures. Also seen were foci of fetal-like squamous epithelium, glandular epithelium, immature mesenchyme, immature cartilage, and neuronal differentiation. Immunohistochemistry performed in three cases showed expression of vimentin, CD99 (MIC2), and neuron-specific enolase in most cells, and focal expression of cytokeratin, epithelial membrane antigen, alpha fetoprotein, glial fibrillary acidic protein, chromogranin, and synaptophysin. The tumors were consistently negative for beta human chorionic gonadotrophin, neurofilament protein, and leukocyte common antigen. The entities considered in the differential diagnosis were poorly differentiated carcinomas, sarcomas, and olfactory neuroblastoma. We suggest that these neoplasms arise from a primitive cell capable of organized divergent differentiation.
我们报告了4例鼻窦畸胎癌肉瘤(SNTCS),这是一种罕见的恶性肿瘤,具有不成熟或恶性畸胎瘤和癌肉瘤的综合特征。患者包括3名男性和1名女性,均为成年人,年龄在21至69岁之间,表现为鼻塞和鼻出血。肿瘤通常由圆形细胞和短梭形细胞组成,并伴有神经外胚层/玫瑰花结样结构。还可见到胎儿样鳞状上皮、腺上皮、未成熟间充质、未成熟软骨及神经分化灶。对3例患者进行的免疫组化检测显示,大多数细胞中波形蛋白、CD99(MIC2)和神经元特异性烯醇化酶呈阳性表达,细胞角蛋白、上皮膜抗原、甲胎蛋白、胶质纤维酸性蛋白、嗜铬粒蛋白和突触素呈局灶性表达。肿瘤β人绒毛膜促性腺激素、神经丝蛋白和白细胞共同抗原检测均为阴性。鉴别诊断考虑的疾病包括低分化癌、肉瘤和嗅神经母细胞瘤。我们认为这些肿瘤起源于能够进行有组织的分化的原始细胞。