Department of Radiology, Columbia University Medical Center, 622 W 168th St, New York, NY 10032, USA.
Radiology. 2013 Jan;266(1):62-71. doi: 10.1148/radiol.12120240. Epub 2012 Oct 15.
Now the leading subtype of lung cancer, adenocarcinoma received a new classification in 2011. For tumors categorized previously as bronchioloalveolar carcinoma (BAC), criteria and terminology had not been uniform, so the 2011 classification provided four new terms: (a) adenocarcinoma in situ (AIS), representing histopathologically a small (≤3-cm), noninvasive lepidic growth, which at computed tomography (CT) is usually nonsolid; (b) minimally invasive adenocarcinoma, representing histopathologically a small (≤3-cm) and predominantly lepidic growth that has 5-mm or smaller invasion, which at CT is mainly nonsolid but may have a central solid component of up to approximately 5 mm; (c) lepidic predominant nonmucinous adenocarcinoma, representing histopathologically invasive adenocarcinoma that shows predominantly lepidic nonmucinous growth, which at CT is usually part solid but may be nonsolid or occasionally have cystic components; and (d) invasive mucinous adenocarcinoma, histopathologically showing lepidic growth as its predominant component, which at CT varies widely from solid to mostly solid to part solid to nonsolid and may be single or multiple (when multifocal, it was formerly called multicentric BAC). In addition, new histopathologic subcategories of acinar, papillary, micropapillary, and solid predominant adenocarcinoma are now described, all as nonmucinous, predominantly invasive, may include a small lepidic component, and at CT are usually solid but may include a small nonsolid component. The micropapillary subtype has a poorer prognosis than the other subtypes. In addition, molecular genetic correlations for the subcategories of adenocarcinoma of the lung are now a topic of increasing interest. As the new classification enters common use, further descriptions of related correlations can be anticipated.
现在,肺癌的主要亚型腺癌在 2011 年有了新的分类。对于以前归类为细支气管肺泡癌 (BAC) 的肿瘤,标准和术语并不统一,因此 2011 年的分类提供了四个新术语:(a) 原位腺癌 (AIS),代表组织病理学上小(≤3cm)、非浸润性贴壁生长,在计算机断层扫描 (CT) 上通常为非实性;(b) 微浸润性腺癌,代表组织病理学上小(≤3cm)和主要贴壁生长,侵袭性 5mm 或更小,在 CT 上主要为非实性,但可能有中央实性成分约 5mm;(c) 贴壁为主非黏液性腺癌,代表组织病理学上的浸润性腺癌,主要表现为贴壁非黏液性生长,在 CT 上通常为部分实性,但可能为非实性或偶尔有囊性成分;(d) 浸润性黏液性腺癌,组织病理学上以贴壁生长为主,CT 表现从实性到主要实性到部分实性到非实性差异很大,可能为单发或多发(多发时称为多灶性 BAC)。此外,现在还描述了新的腺泡、乳头状、微乳头状和实体为主的腺癌组织病理学亚型,均为非黏液性、主要为浸润性,可能包含小的贴壁成分,在 CT 上通常为实性,但可能包含小的非实性成分。微乳头状亚型比其他亚型预后差。此外,肺腺癌亚类的分子遗传学相关性现在是一个越来越受到关注的话题。随着新分类的广泛应用,可以预期会有更多相关相关性的描述。