Pathology and Laboratory Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Hum Pathol. 2011 Dec;42(12):2001-9. doi: 10.1016/j.humpath.2011.02.028. Epub 2011 Jul 20.
Oncocytic mucoepidermoid carcinoma poses diagnostic challenge because of its histologic overlap with other oncocytic salivary gland lesions, including Warthin tumor. Although the prognostic value of the t(11;19) MECT1-MAML2 fusion gene has been established in mucoepidermoid carcinoma, its diagnostic use in discriminating oncocytic mucoepidermoid carcinoma from histologic mimics is unexplored. We evaluated the translocation status in 14 cases of oncocytic mucoepidermoid carcinoma using a MAML2-11q21 break-apart probe spanning the entire chromosome region of the MAML2 gene and correlated these findings with clinicopathologic parameters including age, sex, stage, predominant growth pattern, grade, and p63 immunostaining pattern. All oncocytic mucoepidermoid carcinomas were parotid tumors with a mean patient age of 54.6 years (range, 9-85) and a female to male ratio of 5:2. Grade distribution was as follows: low grade, 9; intermediate grade, 2; and high grade, 3. The histologic patterns observed were as follows: solid, 4; cystic, 8 (of these, 5 had Warthin-like lymphoid stroma); and mixed, 2. Solid oncocytic mucoepidermoid carcinomas showed a diffuse p63 staining pattern, whereas cystic oncocytic mucoepidermoid carcinomas showed staining of the outer layer of intermediate cells ranging from a bilayer to areas of complex multilayering and plaque-like proliferation. Ten (71%) of the 14 cases showed a MAML2 rearrangement by fluorescence in situ hybridization. No correlation was seen between rearrangement status and histologic grade, growth pattern, or p63 staining pattern. However, we demonstrate that the presence of MAML2 rearrangement can be used as supportive evidence to distinguish oncocytic mucoepidermoid carcinoma from other oncocytic lesions.
嗜酸细胞型黏液表皮样癌因其与其他嗜酸细胞性唾液腺病变(包括沃辛瘤)的组织学重叠而具有诊断挑战性。虽然 t(11;19) MECT1-MAML2 融合基因在黏液表皮样癌中的预后价值已得到确立,但它在鉴别嗜酸细胞型黏液表皮样癌与组织学类似物中的诊断用途尚未得到探索。我们使用跨越 MAML2 基因整个染色体区域的 MAML2-11q21 断裂分离探针评估了 14 例嗜酸细胞型黏液表皮样癌的易位状态,并将这些发现与临床病理参数(包括年龄、性别、分期、主要生长模式、分级和 p63 免疫染色模式)相关联。所有嗜酸细胞型黏液表皮样癌均为腮腺肿瘤,患者平均年龄为 54.6 岁(范围 9-85 岁),男女比例为 5:2。分级分布如下:低级别,9 例;中级别,2 例;高级别,3 例。观察到的组织学模式如下:实性,4 例;囊性,8 例(其中 5 例具有沃辛样淋巴间质);混合性,2 例。实性嗜酸细胞型黏液表皮样癌表现出弥漫性 p63 染色模式,而囊性嗜酸细胞型黏液表皮样癌则表现出从中层外层到复杂多层和斑块样增殖的外层中间细胞的染色。14 例中有 10 例(71%)通过荧光原位杂交显示 MAML2 重排。重排状态与组织学分级、生长模式或 p63 染色模式之间未见相关性。然而,我们证明 MAML2 重排的存在可作为支持证据,用于将嗜酸细胞型黏液表皮样癌与其他嗜酸细胞性病变区分开来。