Department of Pathology, Moffitt Cancer Center, Tampa, FL.
Department of Pathology, Stanford University, Palo Alto, CA.
Am J Surg Pathol. 2019 Nov;43(11):1483-1492. doi: 10.1097/PAS.0000000000001309.
Mammary analogue secretory carcinoma (MASC) is a relatively recently described salivary gland adenocarcinoma characterized by ETV6-NTRK3 gene fusion and in most cases indolent clinical behavior. The majority of tumors show an admixture of microcystic, solid, and tubular growth patterns but only a few cases with dominant macrocystic growth have been reported. We report 15 cases of macrocystic MASC. There were 11 men and 4 women (17 to 88 y age range, average 47 y). The patients presented with a painless cystic mass, the majority in the region of the parotid gland (n=13), as well as in submandibular gland (n=1) and the neck (n=1). All tumors were circumscribed measuring 1.0 to 4.0 cm in greatest diameter (mean: 1.75 cm). Twelve tumors were unilocular, while 3 were multilocular. The cystic spaces were predominantly lined by a single epithelial cell layer with focal areas in which the epithelium was multilayered with papillary and hobnail features. In 3 of the cases there were more solid foci of intracystic tumor characterized by papillary and/or microcystic growth. The neoplastic cells were round to oval with hyperchromatic to vesicular nuclei with centrally located nucleoli and eosinophilic or vacuolated cytoplasm. Tumor cells showed strong positivity for S100 protein and mammaglobin, while DOG1 was uniformly negative. A minority of cases showed focal p63 reactivity predominantly limited to the periphery of the cystic lining. ETV6 gene rearrangement was identified in 9 cases. Macrocystic MASC can simulate benign and malignant salivary gland lesions and needs to be included in the differential diagnosis of cystic lesions in the head and neck. To the best of our knowledge, our report represents the first series of macrocystic MASCs wholly focusing on this unusual variant.
乳腺样分泌性癌(MASC)是一种相对较新描述的唾液腺癌,其特征是存在 ETV6-NTRK3 基因融合,且在大多数情况下具有惰性的临床行为。大多数肿瘤表现为微囊状、实性和管状生长模式的混合,但仅有少数以优势大囊状生长为主的病例报道。我们报告了 15 例大囊状 MASC。患者为 11 名男性和 4 名女性(年龄 17 岁至 88 岁,平均年龄 47 岁)。患者表现为无痛性囊性肿块,多数位于腮腺区域(n=13),也有位于下颌下腺(n=1)和颈部(n=1)。所有肿瘤均边界清楚,最大直径为 1.0 至 4.0cm(平均:1.75cm)。12 个肿瘤为单房性,3 个为多房性。囊性腔隙主要由单层上皮细胞衬里,局灶区域上皮呈多层状,具有乳头状和钉突状特征。在 3 例中,有更多的腔内肿瘤实性灶,具有乳头状和/或微囊状生长。肿瘤细胞呈圆形至椭圆形,核染色质深染至泡状,核仁位于中央,胞质嗜酸性或空泡状。肿瘤细胞对 S100 蛋白和乳球蛋白呈强阳性,而 DOG1 呈均匀阴性。少数病例表现为局灶性 p63 反应,主要局限于囊性衬里的周围。9 例存在 ETV6 基因重排。大囊状 MASC 可模拟良性和恶性唾液腺病变,需要纳入头颈部囊性病变的鉴别诊断。据我们所知,我们的报告是首次专门针对这种不常见变体的大囊状 MASCs 系列报告。