Lung Cancer – Imaging features

  • Post author:
  • Post category:POSTS

Lung cancers can be classified into two broad categories: 
1. Small cell lung cancer (20-30%)
2. Non small cell lung cancer (70-80%)
– Squamous cell carcinoma (30-35%)
– Adenocarcinoma ( 35 %)
– Large cell carcinoma (10-15%)

Imaging:

The imaging of lung cancers can be determined on the following points:
A. Shape
B. Calcification and cavitation
C. Ground-glass density, air bronchograms and cyst likely agencies
D. Contrast enhancement
E. Rate of growth
F. Hilar enlargement

A. SHAPE:
Peripheral tumors:

Spherical or ovoid configuration; exceptions pancoast tumors which resembles apical pleural thickening and bronchoalveolar carcinoma and carcinoma arising in the areas of interstitial fibrosis resembling ill-defined area of consolidation.
Lobulated margins have a PPV  80% for a malignant and Spiculated margins have positive predictive value of 33-94 % for malignant potential for a solitary pulmonary nodule.

The term corona radiata indicates multiple strands extending into the surrounding lung because of either tumor extension or fibrotic response to the tumor and is best seen on CT and has a positive predictive value of 33-94 %  for a malignant potential if seen in a solitary pulmonary nodule.
It is not entirely specific for malignant lesions and can be seen in chronic infective process and granulomas.
A single linear band like opacity may be seen in subpleural lesions connecting the lesion to the pleura this is called the pleural tail sign and is nonspecific and can be seen in both benign and malignant pulmonary nodules.

The lung cancers presenting as ill-defined lesions with morphology similar to pneumonia show slow growth over serial CTs and not responding to antibiotics, which in general allows that distinction from infectious pathologies.

The lesions arising in segmental and subsegmental bronchi are seen as soft tissue opacities occluding the affected bronchi with distal dilated bronchi filled with insipiated mucoid secretions. Mucoid impactions result in V or Y – shaped tree in bud densities.

Central tumors:
The main signs of central tumor or collapse and consolidation in the lung parenchyma beyond the tumor and presence of hilar enlargement. Obstruction of a major bronchus may lead to varying amount of collapse-consolidation of the distal lung and thereby making the task of defining the extent of the central tumor lesions within the post obstructive collapse consolidation difficult on non contrast CT. After contrast administration there is differential enhancement, early phases are acquired the neoplastic tissue enhances to a minimal degree whereas distal atelectasis show substantial enhancement.
MRI helps in differentiating the tumor from post obstructive pulmonary changes on T2 and post contrast images. The following features may suggest pneumonia is secondary to an obstructive lesion:
– Alteration in the shape of the collapsed or consolidated lobe directly due to the bulk of the underlying tumor. For eg. Golden S sign.
– Presence of visible mass or irregular stenosis in the main stem or lobar bronchus.
– Presence of an associated central mass.
– A localized pneumonia that remains unchanged for more than 2 weeks or the one that reoccurs in the same lobe.

B. CALCIFICATION AND CAVITATION:

Calcification

Most lung cancers are soft tissue density but some may show partial calcification or cavitation.
CT may show calcification within 6%-10% of bronchogenic carcinomas.
Tumor calcifications are rarely seen on chest radiographs. Mostly the calcification represent pre-existing granulomatous calcifications and golf by the tumor. However, amorphous or cloud like calcification which may be new in onset can be seen in a significant proportion. Calcification can be seen in both small cell and non-small cell carcinomas.

Cavitation:

Cavitation may be seen in lung cancers of any size and are best demonstrated by CT. Thick cavity can be eccentric and the walls of the cavitated tumor are often irregular and the tumor nodules may be visible. Cavitating tumor may also have a smooth inner and outer margin it has been suggested that very thin walled cavity is represent tumor cells lining bullae rather than true cavitation. Fluid levels can also be seen within the necrotic tumor and very rarely it may represent as a mycetoma.
Squamous cell carcinomas are much more likely to cavitate than other cancers in a series of 100 cavitating cancers 82 were squamous cell carcinomas.
Small cell carcinomas for all practical purposes do not cavitate.


C. GROUND-GLASS DENSITY, AIR-BRONCHOGRAMS

The most common type of lung cancer presenting as ground-glass density are lesions of adenocarcinoma with bronchoalveolar cell component or bronchoalveolar carcinoma/ Lepidic growth pattern.
The greater the ground-glass component as compared to a solid component of the lesion better is the prognosis.

6 types of morphological patterns based on histology are classified for Small peripheral the adenocarcinomas:
A: Localized bronchoalveolar carcinoma, LBAC
B: LBAC with foci of structural collapse of alveoli
C: LBAC with foci of active fibroblastic proliferation
D: Poorly differentiated adenocarcinoma
E: Tubular adenocarcinoma
F: Papillary adenocarcinoma with compressive growth pattern

Type A and type B show no lymph node metastasis and have the most favourable prognosis of the 6 types. The follow up recommendations have been laid down by fleischner guidelines 2017.

Air bronchograms :
Adenocarcinomas may contain air bronchograms are cyst like lucencies and hence air bronchogram sign generally associated with infection may also be seen in peripheral cancers presenting as consolidation.

D. CONTRAST ENHANCEMENT

Contrast enhancement exhibits tumoral vascularity. Lung cancers enhance differently from adjacent collapsed and consolidated lung after intravenous contrast injections at both CT and MR imaging and this may be used to differentiate them from adjacent lung collapse on dynamic studies as there is a differential enhancement of the tumor versus the surrounding consolidation.

E. RATE OF GROWTH: 

A solid nodule showing absence of growth for a 2 year period is a relatively reliable indicator for the benign nature of the nodule. However, this criteria is not absolute.
Lesion doubling time for a spherical lesion is usually 25% increase in the diameter and can be used to distinguish benign from malignant lesions; malignant lesions can have doubling time ranging from 30 to 450 days.

F. Hilar enlargement:

Hilar enlargement may be a common feature in radiographs of patients having lung cancer. This may represent the tumor in itself or enlargement of the hilar nodes of metastatic etiology.

Contributed by Dr. Varun Tyagi, Mumbai

References: 

1. Jemal A, Siegel R, Ward E, et al. Cancer statistics. CA Cancer J Clin 2008;58:71–96.
2. Travis WD, Brambilla C, Muller-Hermelink HK, et al. World Health Organization classification of tumours. Pathology and genetics of tumours of the lung, pleura, thymus and heart. Lyon: IARC Press, 2004.
3. MacMahon H, Austin JH, Gamsu G, et al. Guidelines for management of small pulmonary nodules detected on CT scans: a statement from the Fleischner Society Radiology 2005;237:395–400.
4. Takashima S, Sone S, Li F, et al. Small solitary pulmonary nodules (< or =1 cm) detected at population-based CT screening for lung cancer: reliable high-resolution CT features of benign lesions. AJR Am J Roentgenol 2003;180:955–964.
5. Klein JS, Braff S. Imaging evaluation of the solitary pulmonary nodule. Clin Chest Med 2008;29:15–38, v.
6. Libby DM, Smith JP, Altorki NK, et al. Managing the small pulmonary nodule discovered by CT. Chest 2004;125:1522– 1529.
7. Heitzman ER, Markarian B, Raasch BN, et al. Pathways of tumor spread through the lung: radiologic correlations with anatomy and pathology. Radiology 1982; 144:3–14.
8. Kuriyama K, Tateishi R, Doi O, et al. CT-pathologic correlation in small peripheral lung cancers. AJR Am J Roentgenol 1987;149:1139–1143.
9. Aoki T, Tomoda Y, Watanabe H, et al. Peripheral lung adenocarcinoma: correlation of thin-section CT findings with histologic prognostic factors and survival. Radiology 2001;220:803–809. 
10. Mori K, Saitou Y, Tominaga K, et al. Small nodular lesions in the lung periphery: new approach to diagnosis with CT. Radiology 1990;177:843–849.
11. Erasmus JJ, McAdams HP, Connolly JE. Solitary pulmonary nodules. Part II. Evaluation of the indeterminate nodule. RadioGraphics 2000;20:59–66.
12. Grewal RG, Austin JH. CT demonstration of calcification in carcinoma of the lung. J Comput Assist Tomogr 1994;18:867–871.
13. Woodring JH, Fried AM, Chuang VP. Solitary cavities of the lung: diagnostic implications of cavity wall thickness. AJR Am J Roentgenol 1980;135:1269–1271.
14. Ryu JH, Swensen SJ. Cystic and cavitary lung diseases: focal and diffuse. Mayo Clin Proc 2003;78:744–752.
15. Chaudhuri MR. Primary pulmonary cavitating carcinomas. Thorax 1973;28:354–366.
16. Felson B, Wiot JF. Some less familiar roentgen manifestations of carcinoma of the lung. Semin Roentgenol 1977;12: 187–206.
17. Henschke CI, Yankelevitz DF, Mirtcheva R, et al. CT screening for lung cancer: frequency and significance of part-solid and nonsolid nodules. AJR Am J Roentgenol 2002;178:1053–1057.
18. Kuriyama K, Seto M, Kasugai T, et al. Ground-glass opacity on thin-section CT: value in differentiating subtypes of adenocarcinoma of the lung. AJR Am J Roentgenol 1999;173:465–469.
19. Yabuuchi H, Murayama S, Sakai S, et al. Resected peripheral small cell carcinoma of the lung: computed tomographic-histologic correlation. J Thorac Imaging 1999;14: 105–108.
20. Aoki T, Nakata H, Watanabe H, et al. Evolution of peripheral lung adenocarcinomas: CT findings correlated with histology and tumor doubling time. AJR Am J Roentgenol 2000;174:763–768.
21. Noguchi M, Morikawa A, Kawasaki M, et al. Small adenocarcinoma of the lung. Histologic characteristics and prognosis. Cancer 1995;75:2844–2852.
22. Chun EJ, Lee HJ, Kang WJ, et al. Differentiation between malignancy and inflammation in pulmonary ground-glass nodules: the feasibility of integrated (18) F-FDG PET/CT. Lung Cancer 2009;65: 180–186.
23. Funama Y, Awai K, Liu D, et al. Detection of nodules showing ground-glass opacity in the lungs at low-dose multidetector computed tomography: phantom and clinical study. J Comput Assist Tomogr 2009;33:49–53.
24. Kim TJ, Goo JM, Lee KW, et al. Clinical, pathological and thin-section CT features of persistent multiple ground-glass opacity nodules: comparison with solitary ground-glass opacity nodule. Lung Cancer 2009;64:171–178.
25. Lee HJ, Goo JM, Lee CH, et al. Predictive CT findings of malignancy in ground-glass nodules on thin-section chest CT: the effects on radiologist performance. Eur Radiol 2009;19:552–560.
26. Lee KW, Im JG, Kim TJ, et al. A new method of measuring the amount of soft tissue in pulmonary ground-glass opacity nodules: a phantom study. Korean J Radiol 2008;9:219–225.
27. Ohtsuka T, Watanabe K, Kaji M, et al. A clinicopathological study of resected pulmonary nodules with focal pure ground-glass opacity. Eur J Cardiothorac Surg 2006;30:160–163.
28. Park JH, Lee KS, Kim JH, et al. Malignant pure pulmonary ground-glass opacity nodules: prognostic implications. Korean J Radiol 2009;10:12–20.