Sedassari Bruno Tavares, Dos Santos Harim Tavares, Mariano Fernanda Viviane, da Silva Lascane Nelise Alexandre, Altemani Albina, Sousa Suzana
University of São Paulo, School of Dentistry, Department of Oral and Maxillofacial Pathology. Av. Professor Lineu Prestes, 2227, São Paulo, São Paulo, Brazil-CEP: 05508-000.
State University of Campinas, Piracicaba School of Dentistry, Department of Oral Diagnosis. Av. Limeira, 901, Piracicaba, São Paulo, Brazil-CEP: 13414-903.
Ann Diagn Pathol. 2015 Jun;19(3):164-8. doi: 10.1016/j.anndiagpath.2015.03.011. Epub 2015 Apr 6.
In the present study, 3 cases of very rare intraoral carcinomas ex pleomorphic adenomas showing a striking differentiation of the malignant component towards epithelial-myoepithelial carcinoma were described. The tumors occurred in 2 men and 1 woman with median age of 56 years. Involved sites included palate and buccal mucosa. Two patients experienced local recurrences, of which one died of disease complications. In all cases, residual pleomorphic adenoma was present. The malignant component in all cases shared morphological aspects with epithelial-myoepithelial carcinoma. Those areas were characterized by eosinophilic duct-forming cells surrounded by layers of clear cells. The studied immunohistochemical markers highlighted a biphasic cell population. Duct-forming cells expressed pan-cytokeratin, cytokeratin 7, and focally cytokeratin 14, whereas the clear cell component strongly stained to cytokeratin 14, vimentin, and p63 but weakly stained to pan-cytokeratin and focally to α-smooth muscle actin, an immunophenotype compatible with both epithelial and myoepithelial differentiation. The Ki-67 proliferation index was up to 40% in malignant areas. Carcinoma ex pleomorphic adenomas of minor salivary glands with major epithelial-myoepithelial component are rare, locally aggressive, and potentially lethal tumors. The peculiar morphological and immunohistochemical aspects described may raise problems in diagnosis and classification of such cases, particularly in incisional biopsies.
在本研究中,描述了3例非常罕见的多形性腺瘤恶变型口腔内癌,其恶性成分向上皮-肌上皮癌呈现出显著分化。肿瘤发生于2名男性和1名女性,中位年龄为56岁。受累部位包括腭部和颊黏膜。2例患者出现局部复发,其中1例死于疾病并发症。所有病例均存在残留的多形性腺瘤。所有病例中的恶性成分在形态学方面与上皮-肌上皮癌有共同之处。这些区域的特征是嗜酸性导管形成细胞被多层透明细胞包绕。所研究的免疫组化标志物突出显示了双相细胞群。导管形成细胞表达全细胞角蛋白、细胞角蛋白7,局灶性表达细胞角蛋白14,而透明细胞成分对细胞角蛋白14、波形蛋白和p63呈强染色,对全细胞角蛋白呈弱染色,对局灶性α-平滑肌肌动蛋白呈弱染色,这种免疫表型与上皮和肌上皮分化均相符。恶性区域的Ki-67增殖指数高达40%。具有主要上皮-肌上皮成分的小涎腺多形性腺瘤恶变型是罕见的、局部侵袭性且具有潜在致死性的肿瘤。所描述的独特形态学和免疫组化特征可能会给此类病例的诊断和分类带来问题,尤其是在切开活检中。