Early lung cancer with lepidic pattern: adenocarcinoma in situ, minimally invasive adenocarcinoma, and lepidic predominant adenocarcinoma

被引:74
作者
Weichert, Wilko [1 ]
Warth, Arne [1 ]
机构
[1] Heidelberg Univ, Inst Pathol, Heidelberg, Germany
关键词
adenocarcinoma in situ; computed tomography; histology; lepidic; minimally invasive adenocarcinoma; PROPOSED IASLC/ATS/ERS CLASSIFICATION; GLASS OPACITY COMPONENT; INTERNATIONAL-ASSOCIATION; PROGNOSTIC-SIGNIFICANCE; PULMONARY ADENOCARCINOMAS; PATHOLOGICAL CORRELATION; COMPUTED-TOMOGRAPHY; DISEASE RECURRENCE; PREDICTIVE FACTORS; STROMAL INVASION;
D O I
10.1097/MCP.0000000000000065
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Purpose of review This review gives a comprehensive overview on recent developments in the classification of neoplastic lung lesions with lepidic growth patterns, comprising the adenocarcinoma (ADC) precursor lesions atypical adenomatous hyperplasia (AAH), adenocarcinoma in situ (AIS), and minimally invasive adenocarcinoma (MIA) as well as lepidic predominant adenocarcinoma (LPA). Recent findings The concept of a continuum between the precursor lesions AAH and AIS to MIA and frankly invasive ADC is backed by a wealth of recent data showing a gradual decrease in overall survival from 100% for AAH, AIS, and MIA to moderately lower rates for LPA. Further, it has been shown that the morphologic categorization of these tumors can be done with reasonable reliability and that nonmucinous lepidic tumors show distinct molecular alterations with high rates of epidermal growth factor receptor mutations. Importantly, lepidic tumor growth is also mirrored by specific characteristics in computed tomography images, arguing for a combined assessment of histomorphology and imaging data for an optimized classification of lepidic neoplasms. Summary The validity and clinical importance of the novel concept of ADC precursor lesions and LPA have been confirmed by clinical, radiological, morphological, and molecular data. Thereby, it has evolved into a valuable tool to aid in clinical decision-making.
引用
收藏
页码:309 / 316
页数:8
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