Adenocarcinoma of the lung: from BAC to the future
Insights into Imaging volume 11, Article number: 69 (2020)
Adenocarcinoma in situ, minimally invasive adenocarcinoma, lepidic predominant adenocarcinoma and invasive mucinous adenocarcinoma are relatively new classification entities which replace the now retired term, bronchoalveolar carcinoma (BAC). The radiographic appearance of these lesions ranges from pure, ground glass nodules to large, solid masses. A thorough understanding of the new classification is essential to radiologists who work with MDT colleagues to provide accurate staging and treatment. A 2-year review was performed of all surgically resected cases of adenocarcinoma in situ, minimally invasive adenocarcinoma and lepidic predominant adenocarcinoma in our institution. Cases are broken down by age, gender, tumour type and tumour location. A pictorial review is presented to illustrate the radiologic and pathologic features of each entity.
To familiarise radiologists with the new pathological classification of adenocarcinoma of the lung.
To illustrate the varying CT appearances of adenocarcinomas and describe the CT features which correlate with histologic features of invasive growth.
To highlight how the new classification more accurately reflects the correlation between radiology, pathology and prognosis.
The artist formerly known as BAC
A new, international, histopathologic classification of adenocarcinoma of the lung was introduced in 2011 by the International Association for the Study of Lung Cancer (IASLC), American Thoracic Society (ATS) and European Respiratory Society (ERS) .
Adenocarcinoma is the most common histologic type of lung cancer and accounts for over 40% of non-small cell lung cancers .
However, the terminology used to describe it has been inconsistent and non-uniform. For the radiologist, the new classification required some adjustment. The most striking change was the discontinuation of the term bronchoalveolar carcinoma (BAC).
The first descriptions of this entity date back to the late 19th and early 20th centuries when Malassez  and Musser  referred to lung tumours with features of BAC as ‘epithelioma’ and ‘primary cancer of the lung’ respectively. The histological hallmark of these tumours was a prominent bronchioalveolar pattern with variable extension into surrounding tissues.
Subsequent publications described tumours with similar features under a variety of names including ‘alveolar cell tumour of lung’, ‘pulmonary adenomatosis’ and ‘mucocellular papillary adenocarcinoma of the lung’ [5,6,7,8].
In 1960, Liebow  identified BAC as a well-differentiated adenocarcinoma and defined distinct growth patterns:
In contrast to some of his predecessors, Liebow described a potential for pleural invasion, nodal metastases and distant metastases. However, the tumours were considered characteristically slow-growing, particularly the single nodule subtype.
From a pathological standpoint, 3 macroscopic subtypes of BAC were identified :
Localised. A well circumscribed tumour, usually peripherally located, without necrosis or haemorrhage
Multinodular. Miliary nodules involving one or more lobes
Diffuse. An appearance that mimics a pneumonic process, often multilobar
A new classification system was introduced to provide more uniform terminology and diagnostic criteria. Four new entities were proposed: adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA), lepidic predominant adenocarcinoma and invasive mucinous adenocarcinoma.
Adenocarcinoma in situ
Adenocarcinoma in situ is defined as a tumour of ≤ 3 cm with pure lepidic growth but no lymphatic, vascular or pleural invasion and no tumour necrosis. The word lepidic means ‘scaly’ and is used to describe the growth of bland, pneumocytic-type tumour cells along alveoli without lymphovascular invasion.
The typical CT appearance is a ground glass nodule, although part-solid lesions are common as well as lesions with bubble-like internal lucencies.
Minimally invasive adenocarcinoma
Minimally invasive adenocarcinoma is defined as a tumour of ≤ 3 cm with either pure lepidic growth or predominant lepidic growth and ≤ 5 mm of stromal invasion. There is no lymphatic, vascular or pleural invasion and no tumour necrosis. There is 98% overall survival after surgical resection .
The typical CT appearance is a ground glass nodule with a small, central solid component (≤5 mm). When adenocarcinoma of the lung includes invasive and non-invasive components, the invasive component is characteristically solid on CT and the non-invasive component is characteristically hazy and ground glass [13, 14]. The shape of a ground glass nodule does not appear to be helpful in differentiating between AIS and MIA .
Lepidic predominant adenocarcinoma
Lepidic predominant adenocarcinoma is defined as a tumour of > 3 cm in total size and/or has > 5 mm lymphatic, vascular or pleural invasion with a non-mucinous lepidic predominant growth pattern.
The CT appearance is variable but the most typical appearance is a part-solid nodule or mass.
It is recommended that all invasive tumours which were previously known as non-mucinous adenocarcinomas are now described histopathologically according to the predominant subtype :
Lepidic: As discussed above
Acinar: Invasive tumour composed of acini and tubules with columnar or cuboidal cells that resemble bronchial-lining epithelial cells
Papillary: Invasive tumour arranged as papillae structures with a fibrovascular core and complicated secondary and tertiary branches
Micropapillary: Small papillary tufts containing tumour cells with peripheral nuclei but without a fibrovascular core
Lepidic predominant adenocarcinoma has an excellent 5-year survival of 90% after surgical resection . On the contrary, the 5-year survival after surgical resection for the micropapillary subtype is 54% compared with 81% for the non-micropapillary subtypes .
Invasive mucinous adenocarcinoma
Invasive mucinous adenocarcinoma refers to a subtype of invasive adenocarcinomas with apical mucin and small, basally oriented nuclei . These tumours are commonly multicentric, multilobar and bilateral .
The CT appearance of these lesions varies wildly from consolidation and air bronchograms to solid and subsolid nodules and masses with a bronchogenic distribution . Both unifocal and multifocal forms of the disease show a lower lobe predominance (Table 1) .
A taste of our own medicine
A retrospective 2-year review was performed through our institution’s laboratory information system to identify all surgical lung resection specimens for which the final histopathological diagnosis was adenocarcinoma in situ, minimally invasive adenocarcinoma or lepidic predominant adenocarcinoma. The review covered the period January 1, 2017 to December 31, 2018.
There were 35 cases in total which included 24 females and 11 males. The age range was 44 to 86 and the mean age at pathological diagnosis was 69. The cases were divided by histologic subtype into adenocarcinoma in situ (16), minimally invasive adenocarcinoma (13) and lepidic predominant adenocarcinoma (Table 2) (6).
There were 15 tumours resected from the right upper lobe, 8 from the right lower lobe, 7 from the left upper lobe and 5 from the left lower lobe.
The prior CT scans were reviewed in each case to the identify imaging features which may help to classify a lesion as either pre-invasive/minimally invasive or invasive. A pictorial review was created to illustrate the salient learning points for the radiologist.
A pictorial review
Imaging features and prognostication
There are a number of specific features of adenocarcinomas on CT with have been shown to represent favourable and unfavourable prognostic indicators .
Favourable indicators include a ground glass component, bubble-like lucencies, air bronchograms and small size. Unfavourable indicators include thick spiculations, thickened bronchovascular bundles, pleural retraction, concave cuts and large size.
Ground glass attenuation in a nodule correlates with a lepidic growth pattern in the tumour and is associated with a better prognosis . Bubble-like lucencies and air bronchograms are suggestive of a well-differentiated tumour and a favourable prognosis [21, 22].
In contrast, coarse spiculations, thickened bronchovascular bundles and a low proportion of ground glass attenuation in the tumour are associated with a higher incidence of lymph node metastases and vascular invasion . A smooth tumour margin and a ‘solid appearance without air bronchogram’ are suggestive of a poorly differentiated tumour and a poorer prognosis . The presence of a concave cut or notch in the margin of the tumour is also considered an unfavourable prognostic indicator .
The size of a pulmonary nodule has prognostic relevance. For a nodule under 2 cm, the size of the lesion correlates with the incidence of vascular invasion . For a nodule or mass over 3 cm, the size of the lesion correlates with the incidence of central nervous system metastases .
However, there is growing evidence that the solid component of a part-solid nodule is more important than the overall nodule size in staging and prognosis. It has been suggested that a solid component under 3–5 mm can exclude invasive adenocarcinoma, whereas a solid component over 9 mm has 100% specificity for the diagnosis of invasive adenocarcinoma [26, 27].
A larger solid component has more recently been associated with a shorter tumour doubling time, an increased incidence of lymph node metastases and vascular invasion and an increased incidence of local recurrence .
While a more detailed discussion of nodule measurement and follow-up is beyond the scope of this review, suffice is to say that measurement of the solid component of a part-solid nodule rather than the whole nodule is under consideration for the forthcoming IASLC classification. The relative proportion of the solid component in the nodule has also been shown to have prognostic value .
Our review was based on patients in whom a final histopathological diagnosis was made from surgical resection specimens. However, it is worth noting that only 2 of 35 patients in our cohort proceeded directly to surgical resection without a pre-operative biopsy. The remaining 33 patients underwent a CT-guided biopsy to confirm the histopathological diagnosis before resection.
CT-guided biopsies were performed in 8 different centres. One to 3 core biopsies were taken from each patient using 18–20 gauge core biopsy needles.
The biopsy was complicated by a pneumothorax in 10 of 33 patients. Three of these patients required chest drain insertion. The remaining 7 patients required no treatment and were followed up radiologically to resolution.
Thirteen patients had pulmonary haemorrhage which presented as a focal opacity on CT. Two patients had post-procedural haemoptysis and both were managed conservatively (Table 3).
There are two special considerations to be made when contemplating biopsy of a primary lung adenocarcinoma. Every effort should be made to target the solid component of any part-solid nodule, as it is the solid component that represents invasive growth and the ground glass component that represents lepidic growth. Failure to sample the solid component may falsely identify an invasive lesion as a pre-invasive or minimally invasive lesion.
Secondly, every effort should be made to obtain enough tissue for both morphological and molecular/immunohistochemical analysis. This allows testing for mutations, including EGFR and KRAS, which may determine suitability for tyrosine kinase inhibitor therapy. Traditionally, core biopsy has been considered superior to fine needle aspiration (FNA) for morphological analysis but some studies have found FNA to be superior. Rekhtman et al. for example, found FNA cell blocks to be adequate for molecular analysis in 98% of samples . They suggested that the number of tumour cells in a core biopsy may be inadequate due to the large number of stromal cells. By contrast, samples obtained by FNA tend to have a relatively higher number of tumour cells. It is thus useful, where resources allow, to have a cytotechnologist present at the time of the FNA or biopsy to confirm the adequacy of the sample.
There is a new classification system for adenocarcinoma of the lung which has been designed to more accurately reflect the correlation between radiology, pathology and prognosis. The classification describes a spectrum which includes pre-invasive, minimally invasive and invasive lesions. The pre-invasive and minimally invasive lesions have almost 100% survival after surgical resection.
Diagnosis of these lesions is multidisciplinary, but primarily histopathological. The imaging features of lesions on this spectrum vary wildly with a significant amount of overlap. However, the take home message for the radiologist is that certain imaging features, including the size, shape and attenuation of the lesion, will help to determine on which side of the spectrum the lesion is likely to fall. Correct interpretation of the imaging features will help in accurate diagnosis and prognostication.
Availability of data and materials
All data generated or analysed during this study are included in this published article
Atypical adenomatous hyperplasia
Adenocarcinoma in situ
American Thoracic Society
Epidermal growth factor receptor
European Respiratory Society
International Association for the Study of Lung Cancer
Kirsten rat sarcoma viral oncogene homolog
Minimally invasive adenocarcinoma
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Lambe, G., Durand, M., Buckley, A. et al. Adenocarcinoma of the lung: from BAC to the future. Insights Imaging 11, 69 (2020). https://doi.org/10.1186/s13244-020-00875-6
- Lung adenocarcinoma
- Computed tomography
- Subsolid nodules
- Solitary pulmonary nodule