Questions

  • 1.

    Match the abnormal thoracic lucencies seen in Fig. 22.1, A to C , with the following diagnoses.

    • ____ Bilateral pneumothorax.

    • ____ Bullous emphysema.

    • ____ Ruptured subpleural bullae with pneumothorax.

    Fig. 22.1

  • 2.

    Asymmetric air trapping may be confirmed by which of the following radiographic techniques?

    • a.

      Lateral decubitus view.

    • b.

      Forced inspiratory view.

    • c.

      Forced expiratory view.

    • d.

      Overpenetrated view.

    • e.

      Oblique view.

  • 3.

    Mosaic attenuation on high-resolution computed tomography (HRCT) is a common finding in patients with which one of the following diagnoses?

    • a.

      Constrictive bronchiolitis.

    • b.

      Pulmonary embolism.

    • c.

      Panacinar emphysema.

    • d.

      Centrilobular emphysema.

    • e.

      Asthma.

Discussion

The first step in the evaluation of the apparently hyperlucent lung ( Chart 22.1 ) is to check on radiologic technique. A high-contrast, low-kilovoltage (low-kVp) technique may result in a high-contrast chest film and thus obscure the normal vascular markings of the lung, leading to the false impression of hyperlucent lungs. Such highly contrasted radiographs are readily identified by the marked contrast between the soft tissue opacities and the lucency of the lung. This is a particularly common problem with the portable examination, for which high-kVp techniques are more difficult to obtain. The radiologic technique may also result in the appearance of a unilateral hyperlucent lung when the patient is rotated. Rotation produces the unilateral hyperlucent appearance by projecting soft tissues over one side of the chest while rotating the soft tissues off the opposite side of the chest. This latter problem is particularly noticeable in female patients with large pendulous breasts, which add considerably to the opacity over the lower lung fields. Improper centering of the radiographic beam may also cause asymmetric exposure.

Chart 22.1
Hyperlucent Lungs

  • I.

    Bilateral

    • A.

      Faulty radiologic technique (overpenetrated examination)

    • B.

      Thin body habitus

    • C.

      Bilateral mastectomy

    • D.

      Right-to-left cardiac shunts (e.g., tetralogy of Fallot, pseudotruncus arteriosus, truncus type IV)

    • E.

      Pulmonary embolism 396

    • F.

      Emphysema 169 , 174 , 593 , 594

    • G.

      Acute asthmatic attack 175

    • H.

      Acute bronchiolitis (usually in pediatric patients)

    • I.

      Interstitial emphysema 649

  • II.

    Unilateral

    • A.

      Mastectomy

    • B.

      Absent pectoralis muscles

    • C.

      Faulty radiologic technique, including rotation of patient

    • D.

      Extrapulmonary air collections (e.g., pneumothorax, mediastinal emphysema, subcutaneous emphysema)

    • E.

      Pulmonary embolism (acute or chronic) 660

    • F.

      Emphysema (particularly bullous emphysema) 235

    • G.

      Atrophy of trapezius muscle (after radical neck dissection) 568

    • H.

      Bronchial obstruction

      • 1.

        Neoplastic

        • a.

          Bronchogenic carcinoma (rare)

        • b.

          Metastatic (rare, but most common primary tumors are breast, thyroid, pancreas, colon, melanoma) 36

      • 2.

        Granulomatous masses, including broncholith

      • 3.

        Bronchial stenosis with mucocele 574

      • 4.

        Foreign body (common in children)

    • J.

      Hilar mass (e.g., adenopathy, bronchogenic cyst)

    • K.

      Constrictive bronchiolitis (Swyer-James, or MacLeod, syndrome)

    • L.

      Compensatory overaeration

    • M.

      Congenital lobar overdistension

    • N.

      Cardiomegaly (left lower lobe)

Anatomic variations also result in the appearance of hyperlucent lungs. The best-known example is the patient with a very thin body habitus, which results in an overpenetrated chest radiograph. Asymmetric absence of soft tissues can likewise result in unilateral hyperlucent lungs. Radical mastectomy is the most common source of this problem. Rarely, congenital asymmetry of the chest wall results in a similar appearance. This is noted in patients who have hypoplastic or absent pectoralis muscles.

Extrapulmonary air collections, including subcutaneous emphysema, mediastinal emphysema, and pneumothoraces (see Fig. 22.1, B and C ), produce lucent abnormalities that are usually recognized on the basis of their location and are not usually confused with hyperlucent lungs. Most of these conditions result in differences in the opacity of the lung because of overlying soft tissues or their absence. It is important to remember that the radiologic opacity of the normal lung is produced by the pulmonary vascularity. The pulmonary vessels are radiologically identifiable because they contain blood, which is of soft tissue opacity, and are surrounded by air. Therefore, any loss of opacity of the lung reflects a change in the pulmonary vascularity. This should be detected by noting diminution in the size and number of radiologically identifiable vessels ( Fig. 22.2 ). The size and number of radiologically visible vessels are directly related to pulmonary blood flow, supporting the observation that a truly hyperlucent lung is a reflection of decreased blood flow through the lung. This may be the result of cardiac or primary pulmonary disease.

Fig. 22.2, High-resolution computed tomography of a patient with a unilateral, hyperlucent, left lower lobe. Note the asymmetry of the pulmonary vessels with decreased size and number of vessels in the hyperlucent area.

Emphysema

Emphysema is a very important cause of loss of pulmonary vascularity (see Fig. 22.1, A ). 169, 174 Severe cases of emphysema will produce marked attenuation and stretching of pulmonary vessels. This process may be diffuse to such an extent that there may even be nearly complete absence of vessels. The diagnosis of emphysema by evaluation of the pulmonary vascularity requires a subjective evaluation of the vascular patterns. Thurlbeck and Simon 594 evaluated 700 patients in an effort to correlate paper-mounted, whole-lung sections with posteroanterior and lateral view roentgenograms to determine the accuracy of the radiologic diagnosis of emphysema. They measured lung length and width, size of the retrosternal clear space, heart size, and position of the diaphragm. They observed that lung length and the size of the retrosternal clear space increased, the level of the diaphragm was lowered, the heart size decreased, and the lung width was unchanged as the emphysema became more severe. They believed that lung length and diaphragm level were the most discriminating measurements for diagnostic accuracy, followed by size of the retrosternal clear space. However, they identified no combination of these radiologic variables that identified emphysema better than the subjective diagnosis of the disease based on arterial deficiency. They also emphasized that radiologic lung dimensions are related to stature and must therefore be interpreted cautiously. For example, kyphosis of the thoracic spine causes an increase in the anteroposterior diameter of the chest. They further divided vascular patterns into three main categories of abnormality: (1) the vessels are present but narrowed in most of the lung; (2) there is a normal axial pathway but fewer side branches; and (3) there may be complete absence of vessels. While these vascular alterations may be subtle on chest radiograph, HRCT is very sensitive for the detection of variations in regional perfusion and detection of emphysema ( Fig. 22.3, A and B ).

Fig. 22.3, A, Centrilobular emphysema destroys normal lung parenchyma and decreases the pulmonary vasculature. The loss of vasculature accounts for the increased lucency of the lungs on plain film. Plain film is not a sensitive test for the diagnosis of emphysema. B, High-resolution computed tomography (HRCT) of the same patient with centrilobular emphysema shows multiple lucent spaces and minimal vascularity in the anterior lungs, although there are moderately large vessels in the posterior lungs. Also, compare the hyperlucent areas with the opacity of the more normally perfused areas. This makes HRCT a sensitive test for emphysema.

There is hardly any aspect of chest disease that generates more controversy than the role of the radiologist in the diagnosis of emphysema, but most agree that the alterations in pulmonary vascularity are the most reliable radiologic criteria for this diagnosis. When the foregoing criteria are applied, the chest radiograph ( Fig. 22.4 ) is highly specific for the diagnosis of emphysema in patients with advanced disease, but it is not sensitive. HRCT has been shown to be much more sensitive for the diagnosis of early emphysema by demonstrating vascular attenuation, areas of hyperlucency, and small bullae that may be subtle or not detectable by chest radiography. 187, 593

Fig. 22.4, Depression of the diaphragm, a vertically positioned small heart, and hyperlucent lungs caused by the loss of normal vasculature constitute a highly specific appearance for emphysema. These findings indicate advanced disease and are not sensitive for the diagnosis of early emphysema by plain film radiography.

It is important to emphasize that emphysema is an anatomic diagnosis. The morphologic definition of emphysema requires the presence of destruction of alveolar walls and obstruction of small airways. This destruction results in increased size of the distal air spaces. Emphysema is further subdivided into two main types, panlobular (panacinar) and centrilobular (centriacinar). An emphysematous process that destroys all of the lung that is distal to the terminal bronchiole is termed panlobular emphysema, whereas incomplete destruction of lung distal to the terminal bronchiole is termed centrilobular emphysema. The destruction in centrilobular emphysema may occur in the center of the lobule, but may also be eccentrically located. Of the two types, centrilobular is the more common. Other terms frequently confused in the discussion of emphysema are bulla and bleb. A bleb is a collection of air within the layers of visceral pleura, and a bulla is an emphysematous space in the lung parenchyma with a diameter of more than 1 cm; however, these terms are frequently used interchangeably. A bulla represents a distended secondary pulmonary lobule or group of lobules involved by paraseptal or panacinar emphysema. 235 Bullous lesions have a rounded or oval configuration, indicating that there is a significant element of air trapping in the bulla ( Fig. 22.5, A and B ). Bullae must be carefully evaluated because they may be misdiagnosed as pneumothorax (see Fig. 22.1, A ). They may also rupture, causing pneumothorax and a bronchopleural communication, which may be difficult to manage (see Fig. 22.1, B ).

Fig. 22.5, A, Bullous emphysema is a common cause of unilateral or localized hyperlucency. Note attenuation of the right upper vasculature and compression of the right lower lobe. B, Computed tomography confirms the large lucent space replacing the right upper lobe and compressing the middle and lower lobes.

Radiologic distinction of the types of emphysema is frequently impossible, but there are differences in the distribution. Centrilobular emphysema (see Fig. 22.3, A and B ) tends to involve the upper lobes, whereas panacinar emphysema tends to be more severe in the bases ( Fig. 22.6 ). Bullous emphysema may accompany paraseptal or panacinar emphysema (see Fig. 22.1, A and B ).

Fig. 22.6, Coronal computed tomography of a patient with panacinar emphysema, which was caused by alpha-1 antitrypsin deficiency, shows the characteristic basilar distribution of the severe emphysema.

The term chronic obstructive pulmonary disease (COPD) should not be used interchangeably with the term emphysema . 169, 174 The diagnosis of COPD is a clinical diagnosis encompassing the entire group of obstructive pulmonary diseases, including chronic bronchitis, asthma, bronchiolitis obliterans, bronchiectasis, and emphysema. Of these entities, only emphysema results in chronic bilateral loss of pulmonary vascularity and thus results in hyperlucent lungs.

In contrast to the foregoing situation, a severe acute asthmatic attack may cause bilateral air trapping with depression of the diaphragm and hyperlucent lungs, but these changes are reversible.

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