Falk Nadja, Weissferdt Annikka, Kalhor Neda, Moran Cesar A
*Department of Pathology, Tulane University, New Orleans, LA †Department of Pathology, MD Anderson Cancer Center, Houston, TX.
Adv Anat Pathol. 2016 Jan;23(1):13-23. doi: 10.1097/PAP.0000000000000099.
Pulmonary salivary gland-type tumors (SGT) comprise a very small proportion of primary lung neoplasms. The most common tumors among this group are mucoepidermoid carcinoma and adenoid cystic carcinoma. Contrary to the head and neck region, benign SGT such as pleomorphic adenomas are exceedingly rare in the pulmonary system. More recently, 2 additional SGT, namely hyalinizing clear cell carcinoma and salivary duct-like carcinoma were recognized as primary lung tumors expanding the spectrum of SGT that have been described to originate in the tracheobronchial system. Primary pulmonary SGT must be clinically excluded from metastatic salivary gland neoplasms as their morphology is indistinguishable from that of their salivary gland counterparts. Little is known about the clinical behavior and best treatment approach for these unusual tumors. In this review, we provide a comprehensive summary of primary pulmonary SGT with particular emphasis on morphologic characteristics and latest developments in terms of immunohistochemical and molecular techniques.
肺唾液腺型肿瘤(SGT)在原发性肺肿瘤中所占比例极小。该组中最常见的肿瘤是黏液表皮样癌和腺样囊性癌。与头颈部区域不同,良性SGT如多形性腺瘤在肺部系统极为罕见。最近,另外两种SGT,即透明变性透明细胞癌和涎腺导管样癌被确认为原发性肺肿瘤,从而扩大了已描述的起源于气管支气管系统的SGT谱。原发性肺SGT在临床上必须与转移性唾液腺肿瘤相鉴别,因为它们的形态与唾液腺对应肿瘤难以区分。对于这些不常见肿瘤的临床行为和最佳治疗方法知之甚少。在本综述中,我们对原发性肺SGT进行了全面总结,特别强调了形态学特征以及免疫组织化学和分子技术方面的最新进展。