Schwartz Lauren E, Begum Shahnaz, Westra William H, Bishop Justin A
Department of Pathology, The Johns Hopkins University School of Medicine, 401 N. Broadway, Weinberg 2249, Baltimore, MD, 21231, USA,
Head Neck Pathol. 2013 Dec;7(4):311-5. doi: 10.1007/s12105-013-0442-3. Epub 2013 Apr 20.
GATA3 is a zinc finger transcription factor that regulates the normal development of many tissues and cell types. Recent studies have shown that immunohistochemical nuclear staining for GATA3 among tumors is highly restricted to carcinomas of breast and urothelial origin; however salivary gland tumors have not been tested. Given that breast and salivary gland tissues are very similar with respect to embryologic development and structure, we performed GATA3 staining on a spectrum of salivary gland neoplasms. GATA3 immunohistochemistry was performed on a diverse collection of 180 benign and malignant salivary gland neoplasms including 10 acinic cell carcinomas, 2 adenocarcinomas not otherwise specified, 41 adenoid cystic carcinomas, 2 epithelial-myoepithelial carcinomas, 1 low grade cribriform cystadenocarcinoma, 15 mammary analogue secretory carcinomas, 7 metastatic squamous cell carcinomas, 27 mucoepidermoid carcinomas, 2 oncocytic carcinomas, 5 oncocytomas, 34 pleomorphic adenomas, 4 polymorphous low grade adenocarcinomas, 25 salivary duct carcinomas, and 5 Warthin tumors. Staining for GATA3 was observed in 92/180 (51 %) of salivary gland tumors. GATA3 staining was observed in most of the tumor types, but diffuse immunolabeling was consistently seen in salivary duct carcinoma (25 of 25) and mammary analogue secretory carcinoma (15 of 15)-the two tumor types that most closely resemble breast neoplasia. Background benign salivary gland tissue was also usually weakly positive in both acini and ducts. GATA3 immunostaining is not restricted to tumors of breast and urothelial origin. Rather, it is expressed across many different types of salivary gland neoplasms. As a result, salivary gland origin should be considered in the differential diagnosis of a GATA3-positive carcinoma, particularly in the head and neck. Although GATA3 immunohistochemistry is not helpful in resolving the differential diagnosis between a primary salivary gland neoplasm and metastatic breast cancer, it may have some utility in subtyping salivary gland tumors, particularly salivary duct carcinoma and mammary analogue secretory carcinoma.
GATA3是一种锌指转录因子,可调节多种组织和细胞类型的正常发育。最近的研究表明,肿瘤中GATA3的免疫组化核染色高度局限于乳腺和尿路上皮来源的癌;然而,唾液腺肿瘤尚未进行检测。鉴于乳腺和唾液腺组织在胚胎发育和结构方面非常相似,我们对一系列唾液腺肿瘤进行了GATA3染色。对180例良性和恶性唾液腺肿瘤进行了GATA3免疫组化检测,包括10例腺泡细胞癌、2例未另行规定的腺癌、41例腺样囊性癌、2例上皮-肌上皮癌、1例低级别筛状囊腺癌、15例乳腺样分泌癌、7例转移性鳞状细胞癌、27例黏液表皮样癌、2例嗜酸性细胞癌、5例嗜酸性细胞瘤、34例多形性腺瘤、4例多形性低级别腺癌、25例唾液导管癌和5例沃辛瘤。在180例唾液腺肿瘤中有92例(占51%)观察到GATA3染色。在大多数肿瘤类型中都观察到了GATA3染色,但在唾液导管癌(25例中的25例)和乳腺样分泌癌(15例中的15例)中始终可见弥漫性免疫标记,这两种肿瘤类型与乳腺肿瘤最为相似。背景良性唾液腺组织在腺泡和导管中通常也呈弱阳性。GATA3免疫染色并不局限于乳腺和尿路上皮来源的肿瘤。相反,它在许多不同类型的唾液腺肿瘤中都有表达。因此,在GATA3阳性癌的鉴别诊断中应考虑唾液腺来源,特别是在头颈部。虽然GATA3免疫组化无助于解决原发性唾液腺肿瘤与转移性乳腺癌之间的鉴别诊断,但它可能在唾液腺肿瘤的亚型分类中具有一定作用,特别是唾液导管癌和乳腺样分泌癌。