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Medical Radiology · Diagnostic Imaging
Series Editors: H.-U. Kauczor · P. M. Parizel · W. C. G. Peh
Johny A. Verschakelen
Walter De Wever
Computed
Tomography of
the Lung
A Pattern Approach
Second Edition
Medical Radiology
Diagnostic Imaging
Series editors
Hans-Ulrich Kauczor
Paul M. Parizel
Wilfred C.G. Peh
Computed Tomography
of the Lung
A Pattern Approach
Second Edition
Johny A. Verschakelen Walter De Wever
Department of Radiology Department of Radiology
UZ Leuven UZ Leuven
Leuven Leuven
Belgium Belgium
v
vi Preface
lung diseases and of diseases with pulmonary involvement. We have used the
pattern approach because it is well established and is considered a good
method to accomplish the main goal of the book. Our approach also has a
practical orientation. For this reason, a large section of the book is dedicated
to the description of typical and less typical cases. Analysing these cases will
help the reader to exercise pattern recognition and to understand why diseases
present as they do.
Furthermore, we have decided to reduce the number of authors to ensure
that the specific concept and approach of this book are well respected through-
out the whole volume. However, we want to emphasise that this book could
never have been written without the many informative discussions we had on
this topic with radiologists and pulmonologists, both trainees and certified
specialists. We want to express our sincere gratitude to each of them. We
would specially like to thank Dr. Wim Volders and Dr. Johan Coolen for their
valuable suggestions. We also thank Professor Albert L. Baert, who gave us
the unique opportunity to write the first and also the second edition of this
book.
In this second edition, we have maintained the basic structure of the book
which is the pattern approach of lung disease. We have added new insights
that help to explain the CT features responsible for these patterns. We have
also replaced a large number of illustrations by more recent and more illustra-
tive ones. We hope the reader will enjoy this work and will find it helpful
when exploring the perhaps difficult but very exciting CT features of lung
diseases and diseases with a pulmonary component.
Introduction���������������������������������������������������������������������������������������������� 1
Basic Anatomy and CT of the Normal Lung���������������������������������������� 3
How to Approach CT of the Lung?�������������������������������������������������������� 21
Increased Lung Attenuation ������������������������������������������������������������������ 33
Decreased Lung Attenuation������������������������������������������������������������������ 55
Nodular Pattern��������������������������������������������������������������������������������������� 81
Linear Pattern������������������������������������������������������������������������������������������ 103
Combined Patterns���������������������������������������������������������������������������������� 125
Case Study������������������������������������������������������������������������������������������������ 137
Index���������������������������������������������������������������������������������������������������������� 223
vii
Introduction
The use of computed tomography in the study of improved detail of high-resolution computed
lung diseases is well established. Many reports tomography, but also the ability to produce highly
have indeed emphasised its role not only in the detailed reformatted images is responsible for
detection and diagnosis but also in the quantifica- this.
tion and follow-up of both focal and diffuse lung CT is now able to study the lung anatomy and
diseases. Moreover, CT has helped to better pathology at the level of the secondary pulmo-
understand the clinical and pathological course nary lobule, which is a unit of lung of about
of some diseases, while some CT classifications 0.5–3 cm. CT can discover different components
are used now to categorise disease. of this secondary pulmonary lobule, especially
CT interpretation, however, remains difficult. when they are abnormal. This is particularly
CT findings are often not specific and can change helpful in the study of the distribution pattern of
during the course of the disease. In addition, the the disease since the airway, vascular, lymphatic
CT changes often have more than one pathologi- and intestitial pathways of distribution can,
cal correlate, abnormalities can occur before because of their specific relation to the secondary
clinical symptoms develop, and clinical symp- pulmonary lobule, often be identified and differ-
toms may be present before CT abnormalities entiated from each other. This explains why the
become evident. That is why a final diagnosis, diagnosis of lung disease with CT is to a large
especially in a patient with diffuse interstitial extent based on the study of the distribution of
lung disease, is often only possible when clini- the disease.
cians, pathologists and radiologists work closely Another important element to diagnosing
together. To make such multidisciplinary coop- lung disease with CT is the study of the disease
eration successful, it is very important that the appearance pattern. Recognition of the appear-
pathological correlate of the CT changes is very ance pattern often allows developing an appro-
well understood. In fact, when looking at the CT priate differential diagnosis list including all the
features, at least at a submacroscopic level, one major categories of disease that might lead to the
should be able to predict the pathological identified pattern. Although the recognition of a
changes, but also vice versa, when reading the pattern may be easy and straightforward, some
report of the pathologist, one should be able more lung changes are difficult to categorise because
or less to imagine how the CT scan could look. patterns are very often mixed or change during
Today’s CT techniques can offer such good the course of the disease. Nevertheless, in order
image quality that these correlations between CT to make a diagnosis or an adequate differential
and pathology become easier. Not only the diagnosis list, the exercise of trying to categorise
the CT changes into one or more specific pat- should be identified. In each chapter, a great deal
terns should always be done. This is certainly of attention is therefore provided on how combin-
true when diffuse lung disease is studied but is ing disease pattern and distribution pattern can
often also very helpful when focal lung disease lead to a diagnosis or a narrow differential diag-
or diseases involving only a few lung areas are nosis list. Diagrams are provided for this purpose.
encountered. A good understanding of the disease and distri-
The subtitle of this book is “A pattern bution pattern is only possible when the anatomy
approach”. Indeed an important objective of this of the lung is well known. That is why a chapter
book is to help the reader to identify the disease on basic anatomical considerations is included
pattern, i.e. the appearance and distribution pat- and precedes the chapters dealing with the differ-
tern of the disease. Tools and illustrations pro- ent patterns. Finally, the CT features of the most
vided not only help to recognise these patterns frequently occurring focal and especially diffuse
but also help to understand why disease can lung diseases will be shown, and their appearance
present with a particular pattern. The book is and distribution patterns will be listed.
organised according to the different appearance
patterns that can be encountered on a CT scan of
the lungs. After an introductory chapter on how Basic Objectives of the Book
a CT of the lung should be approached, several • Learn to detect and understand the CT
chapters describe the different patterns in detail: changes in patients with lung disease
(1) increased lung attenuation, (2) decreased lung • Learn to recognise and to determine the
attenuation, (3) the nodular pattern and (4) the lin- different appearance and distribution
ear pattern. Because some lung diseases typically patterns of lung disease
combine two ore more patterns simultaneously, • Learn to use these patterns to make a
also a chapter is added that deals with combined diagnosis or to narrow the differential
or mixed patterns. Once the appearance pattern(s) diagnosis list
is/are determined, the distribution pattern(s)
Basic Anatomy and CT
of the Normal Lung
Contents Abstract
1 Introduction 3 A good knowledge of the lung anatomy in
general and a good understanding of the anat-
2 Basic Anatomical Considerations 4
2.1 Anatomic Organisation of the Airways omy of the secondary pulmonary lobule in
and Airspaces 4 particular is mandatory to understand the CT
2.2 Anatomic Organisation of the features of the normal and the diseased lung.
Blood Vessels 5
In the first section of this chapter, the basics of
2.3 Anatomic Organisation of the Lymphatics 7
2.4 The Pulmonary Interstitium 8 lung anatomy will be discussed. In the second
2.5 The Subsegmental Structures of the Lung section, a description will be given on the rela-
and the Secondary Pulmonary Lobule 9 tionship between lung anatomy and distribu-
3 Relationship Between Anatomy tion of disease while in the third section the
and Distribution of Disease 12 CT features of the normal lung will be
4 CT Features of the Normal Lung 13 explained.
4.1 Large Arteries and Bronchi 13
4.2 Secondary Pulmonary Lobule 15
4.3 Lung Parenchyma 16
References 17 1 Introduction
Segmental bronchus
Subsegmental bronchus
Bronchus
Bronchi
Lobular Bronchiole
Terminal bronchioles
Respiratory bronchiole
Alveolar Duct
Secondary
Pulm Lobule
Alveolar sac
Ac
nu
i
Table 1 In this table the different generations of airways nition is more practical and more frequently used
with their approximate diameter are listed in radiological literature. The lobular bronchioles
Structure Diameter (mm) enter the core of the secondary pulmonary lobule
Trachea 25 and divide into a number of terminal bronchioles
Main bronchi 11–19 according to the size of the lobule. These termi-
Lobar bronchi 4–13 nal bronchioles represent the most distal purely
Segmental bronchi 4–7 conducting portion of the tracheobronchial tree;
Subsegmental bronchi 3–6 that is, they conduct air without being involved
Bronchi 1.5–3 in gas exchange. The terminal bronchioles give
Terminal bronchi 1 rise to the respiratory bronchioles, which are so
Bronchioles 0.8–1 designated because alveoli bud directly from their
Lobular bronchioles 0.8 walls. Hence, respiratory bronchioles not only are
Terminal bronchioles 0.6–0.7 conducting but are also involved in gas exchange.
Respiratory bronchioles 0.4–0.5 The respiratory bronchioles give rise to alveolar
Alveolar ducts and sacs 0.4
ducts. In contrast to the respiratory bronchioles
Alveoli 0.2–0.3
where alveoli only rise occasionally from the
wall, these alveolar ducts have so many alveoli
(Horsfield and Cumming 1968). The initial belief originating from their wall that there is virtually
that the distance along the airways from the tra- no wall structure between the alveolar orifices.
chea to terminal gas exchanging units is approxi- The alveolar ducts finally lead into the alveolar
mately the same for the entire lung is probably a sacs containing several alveoli (Boyden 1971).
gross oversimplification (Weibel 2009). Indeed,
the number of generations is different throughout
the lung and varies between approximately 9–23 The lobular bronchioles enter the core of
making the distance along the airways from the the secondary pulmonary lobule and divide
trachea to the terminal gas exchanging units also into a number of terminal bronchioles
variable. The trachea divides into main bronchi according to the size of the lobule.
that divide into lobar bronchi. The lobar bronchi
divide into segmental bronchi that in turn divide
into subsegmental bronchi. These bronchi divide Adjacent alveoli originating from different air
into several generations of smaller bronchi and sacs are known to communicate directly with one
finally the terminal bronchi are reached. These another through the pores of Kohn. Familiarity
terminal bronchi divide into bronchioles. with these tiny communications is necessary to
Bronchioles differ from the bronchi in that the understand the pathology of diseases involving
bronchi contain cartilage and glands in their walls, the alveoli (Culiner and Reich 1961; Hogg et al.
whereas the bronchioles do not. The bronchioles 1969; Liebow et al. 1950; Van Allen and Lindskog
include two categories: the membranous bron- 1931). The canals of Lambert communicate dis-
chioles (lobular and terminal) and the respiratory tal bronchioles, particularly preterminal bronchi-
bronchioles. The term “small airways” is often oles with alveoli (Lambert 1955).
also used to describe the bronchioles and small
airway disease is then defined as the pathological
condition in which the bronchioles are affected. 2.2 Anatomic Organisation
At this point, it should be emphasised, however, of the Blood Vessels
that an internal diameter of 2 mm is another often
used division between small and large airways. The arteries of the human lung accompany the air-
Although both definitions do not correspond ways and their pattern of division is similar to the
because cartilage may be found in some peripheral branching of the airways; hence for each airway
airways less than 1 mm in diameter, the latter defi- branch there is a corresponding artery (Elliott and
6 Basic Anatomy and CT of the Normal Lung
Fig. 2 Anatomic
organisation of the blood
vessels
Veins
Arteries
Venules
Secondary
Pulm Lobule
Ac
nu
i
s Capillary
Arterioles network
Reid 1965) (Fig. 2). However, there are many Distal to the capillary network, the pulmo-
artery branches that do not accompany any portion nary venules are formed, which merge into pul-
of the airway and that are sometimes called super- monary veins at the periphery of the secondary
numerary arteries (Fraser and Pare 1977). This is pulmonary lobule. These pulmonary veins run
especially seen at the most distal part of the bron- through the interlobular septa and then through
chovascular tree. The vessels accompanying the more central connective tissue sheaths to the left
bronchi are considered to be elastic arteries atrium.
because they have well-developed elastic laminae.
The vessels accompanying the bronchioles down
to the level of the terminal bronchioles are gener- The pulmonary veins are formed by conflu-
ally considered to be muscular arteries because ence of pulmonary venules at the periphery
they contain fewer elastic laminae. The vessels of the secondary pulmonary lobule and run
distal to the terminal bronchioles lose their con- through the interlobular septa and through
tinuous muscular coat and have a single elastic more central connective tissue sheets.
lamina; they are called pulmonary arterioles. The
capillary network originates from the arterioles
and surrounds the alveoli. The high number of The bronchial arteries belong to a different
individual very small vessels make this capillary arterial system that originates from the systemic
network look like a thin, continuous layer of blood circulation. Except for those distributed to the
covering alveoli interrupted by columns of con- pleura, these bronchial arteries accompany the
nective tissue that act as supports (Weibel 1979). bronchi to the level of the terminal bronchiole. At
this point they ramify into a capillary plexus,
which is intimately integrated into the bronchiolar
The arteries of the human lung accompany wall. In the lung periphery, the bronchial arteries
the airways and their pattern of division also anastomose and are drained by the pulmo-
is—except for the most distal part—simi- nary venous system (Lauweryns 1971; Miller
lar to the branching of the airways. 1947). The bronchial veins exist as a distinct set
of vessels only in the hilar region, where they
2 Basic Anatomical Considerations 7
drain blood from the hilar structures and walls of and blood vessel surrounded by lymphatics. No
the major bronchi into the azygos and hemiazygos lymphatics are found in alveolar walls. This is
system. It is not clear whether there are also bron- curious considering that their job is to mobilise
chial veins at the periphery of the lung that drain fluid that is escaping from the capillaries. So this
blood from the bronchial capillary bed into pul- fluid has to migrate towards the pulmonary lym-
monary veins. However, it is generally accepted phatics, which are located in the peribronchiolar
that the final drainage of the bronchial arterial and the perivascular spaces, the interlobular septa
flow is by way of the pulmonary veins. and the pleural network (Weibel and Bachofen
1979). Consequently, one part of the lymph fluid
is removed first centrifugally and then centripe-
2.3 Anatomic Organisation tally while another part is removed directly
of the Lymphatics towards the hilum. It is not clear whether the cap-
illary pressure forces this fluid through the alveo-
The pulmonary lymphatics absorb the normal lar walls to the lymphatics that act as efficient
transudate from the capillary bed and carry it sumps or whether the fluid is sucked into the
from the interstitial space to the central circula- lymphatics by more negative interstitial pressure
tion (Fig. 3). There are two intercommunicating (Weibel and Bachofen 1979). Probably both
networks of lymph flow. First there is the rich mechanisms are operational.
subpleural plexus, which is connected to and
drained by the septal lymphatic channels. These
channels follow interlobular septa and progress There are two intercommunicating net-
into axial connective tissue sheaths around veins works of lymph flow:
as they progress centrally. Another system of • The subpleural plexus connected to sep-
lymphatic channels is found in the axial connec- tal lymphatic channels
tive tissue around arteries, bronchi and bronchi- • The axial plexus around arteries, bron-
oles with the terminal bronchiole and its chi and bronchioles
accompanying arteriole as the most distal airway
Lymphatics
Secondary
Pulm Lobule
Ac
nu
i
s
Fig. 3 Anatomic
organisation of the
lymphatics
8 Basic Anatomy and CT of the Normal Lung
Secondary
Pulm Lobule
Parenchymatous
Connective Tissue
Fig. 4 The pulmonary
interstitium
2 Basic Anatomical Considerations 9
2.4.2 Axial Connective Tissue et al. 1967; Sargent and Sherwin 1971; Weibel
The axial connective tissue is a system of fibres and Taylor 1988; Ziskind et al. 1963).The pri-
that originates at the hilum, surrounds the bron- mary pulmonary lobule cannot be demonstrated
chovascular structures and extends peripherally. by CT in normal states, but its borders may some-
It terminates at the centre of the acini in the form times be suggested. Also the acinus can some-
of a fibrous network that follows the wall of the times be identified with CT in diseased lung. But
alveolar ducts and sacs (Weibel 1979). The alve- especially the secondary pulmonary lobule or
oli are formed in the meshes of this fibrous parts of it are very often seen with this technique,
network. even when the lung is only mildly diseased or
normal. That is why the secondary pulmonary
2.4.3 Parenchymal Connective Tissue lobule is the ideal unit of subsegmental lung
At their peripheral limits, the alveoli and the cap- organisation with which the CT and pathologic
illaries are in close contact in order to allow gas abnormality can be correlated and why a basic
diffusion. Nevertheless, elastic and collagen understanding of its anatomy is mandatory to
fibres are present also and are part of the paren- understand the CT patterns seen in various dis-
chymatous connective tissue. These fibres appear ease states.
at the side of the capillaries; in fact, the capillary
is wound around these fibres like a snake around
a pole. In this way, on one side of the capillary The secondary pulmonary lobule is the
the basement membrane of this capillary is fused ideal unit of subsegmental lung organisa-
to the alveolar basement membrane to form a thin tion with which the CT and pathologic
sheet across which diffusion takes place, while abnormality can be correlated.
on the other side a septal fibre separates both
structures. These fibres extend from the axial to
the peripheral connective tissue and are short and
thin (Weibel 1979). 2.5.1 Primary Pulmonary Lobule
Miller originally described the primary pulmo-
nary lobule and defined it as the lung unit distal to
The pulmonary interstitium is the support- the respiratory bronchioles (Miller 1947). The
ing tissue of the lung and can be divided primary pulmonary lobule consists of alveolar
into three component parts that communi- ducts, alveolar sacs and alveoli. According to
cate freely: Wyatt et al., approximately 30–50 primary pul-
• the peripheral connective tissue monary lobules can be found in one secondary
• the axial connective tissue pulmonary lobule (Wyatt et al. 1964).
• the parenchymal connective tissue
2.5.2 Acinus
Although several different definitions of the aci-
nus can be found, a commonly accepted, and also
2.5 he Subsegmental Structures
T for CT interpretation conceptually appropriate,
of the Lung and the definition describes the acinus as the portion of
Secondary Pulmonary Lobule lung distal to a terminal bronchiole and supplied
by a first-order respiratory bronchiole or bronchi-
Three units of lung structure have been described oles (Gamsu et al. 1971; Recavarren et al. 1967;
at the subsegmental level of the lung: the primary Reid and Simon 1958). Because respiratory bron-
pulmonary lobule, the acinus and the secondary chioli contain alveoli in their wall, the acinus is
pulmonary lobule (Gamsu et al. 1971; Lui et al. the largest unit in which all airways participate in
1973; Miller 1947; Pump 1964, 1969; Recavarren gas exchange. The reported number of acini in
10 Basic Anatomy and CT of the Normal Lung
a b 1
3
3
1
3
2
1
3
1
Fig. 6 a–c. (a) Sagittal section through the lung. Several accompanying arteries (red) with adjacent to them some
interlobular septa can be recognised both in the lung supporting connective tissue (not indicated) and some
parenchyma and at the lung surface (arrows) demarcating lymph vessels (green). The lobular parenchyma consists
secondary pulmonary lobules. (b) The secondary pulmo- of functioning lung supported by connective tissue septa
nary lobule has three principal components: (1) the inter- (white) and stroma. Figure 6a appears courtesy of
lobular septa, (2) the centrilobular region and (3) the B. Vrugt (Institute for Pathology, University Hospital
lobular lung parenchyma. (c) The interlobular septa con- Zürich, Switzerland). Part of Fig. 6b and c appear cour-
tain pulmonary veins (blue) and lymphatics (green) sur- tesy of E. Verbeken (Dept. of Pathology, University
rounded by connective tissue (white). The centrilobular Hospitals Leuven, Belgium)
region contains bronchiolar branches (yellow) with their
one secondary pulmonary lobule varies consider- components of the lobule is quite precise and is
ably in different studies and numbers are found similar from lobule to lobule.
between 3 and 12. The diameter of an acinus has The secondary pulmonary lobules are demar-
been reported to be between 5 and 10 mm (Pump cated from each other by interlobular connective
1969; Sargent and Sherwin 1971) (Figs. 6 and 7). tissue septa: the interlobular septa. As mentioned
earlier, it is not clear whether fibrous strands also
2.5.3 Secondary Pulmonary Lobule penetrate from these interlobular septa into the
The secondary pulmonary lobule is defined as the lobule between the acini (Weibel 1979) inducing
smallest unit of lung structure marginated by “fibrous” intralobular septa or whether the space
connective tissue septa (Heitzman 1984) (Fig. 6). in between the acini is only a “virtual” interstitial
It is supplied by a group of terminal bronchioles, space between two unit structures (Johkoh et al.
is irregularly polyhedral in shape and is approxi- 1999). The interlobular septa are clearly continu-
mately 1–2.5 cm on each side (Reid and Simon ous peripherally with the pleura (Fig. 6a). They
1958). Although the overall configuration of the are, however, not homogeneously developed in
secondary pulmonary lobule and its relationship the lung. The septa in the upper lobes tend to be
to other lobules appears to be almost entirely ran- longer and more randomly arranged, whereas in
dom, the organisation of the individual anatomic the lower lung fields they appear to be shorter
2 Basic Anatomical Considerations 11
a b
Fig. 7 (a) Detail of a secondary pulmonary lobule show- lobule. TB terminal bronchiole, RB respiratory bronchi-
ing one acinus. TB terminal bronchiole, RB respiratory ole, AD alveolar duct, IV interlobular septal vein; arrows
bronchiole, AD alveolar ducts, AS/ALV alveolar sacs/ interlobular septa
alveoli. (b) MicoCT of a part of the secondary pulmonary
and more horizontally oriented perpendicular to when it divides, it most often divides into two
the pleural surfaces. branches of different sizes, with one branch nearly
These connective tissue septa are also better the same as the one it arose from and the other
developed at the lung periphery than in the cen- smaller (Itoh et al. 1993). This lobular bronchiole
tral portions of the lung. But even at the lung is distributed with the accompanying artery, which
periphery, the interlobular septa do not always has the same irregular dichotomous branching into
constitute a totally intact connective tissue enve- the central portion of the lobule. Thus on CT, there
lope surrounding the secondary pulmonary lob- often appears to be a single dominant bronchiole
ule. There are indeed occasional defects in the and artery in the centre of the lobule, which gives
septa allowing communication between lobules off smaller branches at intervals along its length.
(Heitzman 1984). These defects have radiologi- These bronchioles progress through the lobule,
cal significance for the concept of collateral air- dividing progressively from terminal to respira-
flow on a segmental level. Indeed collateral tory bronchioles, alveolar ducts, alveolar sacs and
airflow can maintain lung segments in an inflated alveoli. Although the arteries accompany the bron-
state despite obstruction of their bronchi. It is chioles until the centre of the lobule, their branch-
believed that the pores of Kohn and the canals of ing pattern throughout the lobule is somewhat
Lambert are responsible for this phenomenon. If different from the bronchiolar branching pattern.
there were no defect in the interlobular septa col- However, finally these vessels terminate in the
lateral airflow would only be possible within the capillary bed, which is distributed throughout the
secondary pulmonary lobule. alveolar wall. Blood then flows from the capillary
As mentioned earlier, the airway component of bed into venules, which drain to the periphery of
the lobule is supplied by a group of terminal bron- the lobule where they join to form the pulmonary
chioles. However, it is difficult to define which vein. These pulmonary veins course centrally
bronchial structures precisely supply the lobules through the interlobular septa.
(Itoh et al. 1993). Branching of the lobular bron- So branching continues until ultimately the
chiole is irregular dichotomous, which means that entire lobulus is supplied. Most of the lobular
12 Basic Anatomy and CT of the Normal Lung
These structures are also believed to be respon- perivascular and peribronchial connective tis-
sible for the collateral air drift. This collateral air sues. Similarly, diseases of the pulmonary lym-
drift is thought to prevent or to minimise atelec- phatics that run in the interlobular septa and
tasis secondary to obstruction of terminal por- along the vessels and airways will cause thicken-
tions of the airway by providing an alternate ing of these structures. Since pulmonary veins
route for air to reach the lung distal to the obstruc- run in the interlobular septa, it is to be anticipated
tion. The air that reaches the alveoli by collateral that disease processes involving the pulmonary
air drift, however, shows relatively little move- veins also initially will appear as interstitial
ment during respiration and the oxygen in this abnormalities.
stagnant air becomes absorbed, leading to low As we will see further on in this book, the CT
oxygen concentrations in alveoli and secondary interpretation of lung disease is in part based on
to hypoxic vasoconstriction. It should be empha- the recognition of the location of the diseases in
sised that collateral air drift not only occurs relation to these different components of the sec-
between adjacent alveoli within one secondary ondary pulmonary lobule structures.
pulmonary lobule but occurs also between lob-
ules, segments and even lobes. This can be
explained by the well-known incompleteness of 4 T Features of the Normal
C
fissures and by the presence of defects in the Lung
interlobular septa. The canals of Lambert offer
another pathway by which diseases can be dis- 4.1 Large Arteries and Bronchi
tributed and by which collateral airflow can
occur. The large pulmonary arteries normally appear
The unequal size of the airspaces may be as rounded or elliptic opacities on CT when
responsible for another phenomena that can imaged at an angle to their longitudinal axis and
explain the distribution pattern of some diseases. roughly cylindrical when imaged along their
Small alveoli are located in the walls of the larger axis (Fig. 8). These arteries are accompanied by
alveolar ducts and alveolar sacs. Alteration in thin-walled bronchi of which the appearance is
pulmonary surfactant can cause increase in sur- also defined by the angle between the scan plane
face tension in the alveoli which may, due to and the axis of the bronchi. When imaged along
Laplace law, be responsible for collapse of small their axis, bronchi and vessels can show a slight
alveoli onto the larger alveolar ducts and sacs. tapering as they branch. The diameter of the
Since small alveoli are predominantly located in artery and its neighbouring bronchus should be
the peripheral parts of the acini, this collapse will approximately equal. However, in the depen-
predominantly take place at the borders of the dent areas vessels are usually slightly larger
acini (Galvin et al. 2010). (Fig. 8a). It should be emphasised that in normal
Also the arterial supply is distributed to the subjects, bronchi may appear larger than their
central core portion of the secondary pulmonary adjacent arteries (Lynch et al. 1993). This is cer-
lobule, which explains why some pathologic pro- tainly true when the scan traverses the bronchus
cesses involving the pulmonary arterial and cap- just before it branches (Fig. 8b). The outer walls
illary bed such as pulmonary infarction and of both the vessels and the bronchi should be
pulmonary haemorrhage initially can present smooth and sharply defined. Also the inner wall
findings of alveolar disease that again involve the of the bronchi should appear smooth and of uni-
secondary pulmonary lobule from its core to its form thickness. Whether a normal airway is vis-
peripheral parts leaving the septal structures ible or not on a CT scan depends on its size and
unaffected. on the CT technique that is used. As a general
On the other hand, diseases that cause intersti- rule, airways less than 2 mm in diameter or
tial abnormalities and fibrosis will produce thick- closer than 1–2 cm to the pleural surface are
ening of the septa, the alveolar wall and the below the resolution of even HRCT images
14 Basic Anatomy and CT of the Normal Lung
a b
Fig. 8 HRCT of the normal lung at suspended deep inspi- Some bronchi appear larger than their adjacent arteries
ration. Notice that the vessels are slighter larger in the because the scan traverses the bronchus just before it
dependent areas than in the non-dependent areas (a). branches (arrow in b)
(Kim et al. 1997; Murata et al. 1986, 1988; and inappropriate window settings can alter
Webb et al. 1988) (Table 1). The presence of the thickness of the bronchial wall (Webb et al.
visible bronchial structures in the lung periph- 1984). No absolute window settings can be rec-
ery (within 2–3 cm of the chest wall) signifies ommended because of variation between CT
pathologic bronchial wall thickening or ectasia machines and individual preferences; however,
of the small airways. for diagnostic purposes consistent window
Assessment of the bronchial wall thickness settings from patient to patient are advisable
is often considered a difficult task because it is and a window centre between –300 and –950
subjective and depends on the window settings. Hounsfield Units (HU) with corresponding
In addition, what is seen as bronchial wall also window widths between 1000 and 1500 HU
includes the peribronchovascular interstitium; has been recommended (Bankier et al. 1996;
consequently, thickness is always a little over- Grenier et al. 1993; Kang et al. 1995; Seneterre
estimated. In general and for bronchi distal to et al. 1994).
the segmental level, the wall thickness of the Although expiration has an important effect
airways is approximately proportional to their on the diameter of the trachea—the anteroposte-
diameter measuring from one-sixth to one-tenth rior diameter can decrease up to 32% between
of their diameter (Matsuoka et al. 2005; Weibel deep inspiration and deep expiration due to the
and Taylor 1988). The ability to visualise air- invagination of the posterior tracheal mem-
ways also reflects the choice of appropriate brane—the diameter of the main and lobar bron-
window settings. These window settings have a chi appears only slightly reduced on full
marked effect on the apparent size of structures expiration CT scans (Stern et al. 1993).
4 CT Features of the Normal Lung 15
a b
Fig. 9 (a) CT of the normal lung (coronal reconstruc- heads) (b) CT of the lung (coronal reconstruction) of a
tion). Interlobular septa can often be inferred by locating patient with lymphangitic spread of cancer and thickening
septal pulmonary vein branches (arrows) presenting as of the interlobular septa in the right lower lobe. Because
linear, arcuate or branching structures approximately of this thickening the secondary pulmonary lobules can be
5–10 mm from the centrilobar arteriole (white arrow- better recognised
16 Basic Anatomy and CT of the Normal Lung
a b
c d
Fig. 11 (a–f) HRCT of the normal lung at upper and dient between the dependent and the nondependent lung,
middle levels in supine and at lower level in prone body which is larger on expiratory scans than on inspiratory
position (a, b, c, suspended deep inspiration; d, e, f same scans
levels, suspended deep expiration). Notice the density gra-
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Fig. 11 (continued)
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How to Approach CT of the Lung?
Contents Abstract
1 Introduction 21 This chapter introduces the three pillars on
which the diagnosis of lung disease on a chest
2 Analysis of Patient Data 23
CT is based: the recognition of the appearance
3 Appearance Pattern of Disease 23 pattern, the study of the location and distribu-
3.1 Increased Lung Attenuation 23
tion pattern of the abnormalities in the lung
3.2 Decreased Lung Attenuation 25
3.3 Nodular Pattern 28 (distribution pattern) and the careful analysis
3.4 Linear Pattern 28 of the patient data.
3.5 Combination of Patterns 29
4 Localisation and Distribution of Disease:
Distribution Pattern 31
References 32 1 Introduction
Fig. 1 Three basic elements on which diagnosis of lung disease with CT is based
this discussion the radiologist should give the give detailed macroscopic and submacroscopic
most likely radiological diagnosis or differential insight into how the lung is affected by the dis-
diagnosis which is based on the CT presentation ease and usually further reduces the differential
and on the clinical data available at that moment. diagnosis list and sometimes even allows making
Generally the diagnosis of lung disease on a a specific diagnosis.
chest CT is based on three elements (Fig. 1): In a third step, a careful analysis of the patient
data that are available is necessary and includes
• Recognition of the appearance pattern of dis- first the study of additional radiological informa-
ease, i.e. classifying the abnormalities in a cat- tion that is available on this and on previous radio-
egory that is based on their appearance logical exams. Examining the present CT scan for
• Determination of location and distribution of other than lung changes can indeed be very help-
the abnormalities in the lung: the distribution ful to further narrow the differential diagnosis. For
pattern example, the simultaneous detection of osteolytic
• Careful analysis of the patient data that are lesions in the ribs and nodules in the lung could
available at the time the CT scan is performed suggest metastatic disease. In addition, the exami-
nation of serial CT examinations, when available,
In a first step, the reader should try to recog- is very helpful when, for example, examining
nise the appearance pattern of the lung changes lesion growth. It can, however, also be interest-
because recognising this pattern makes it pos- ing to wait for follow-up images before decid-
sible to develop a first and appropriate dif- ing on the diagnosis. In an intensive care patient,
ferential diagnosis list, including the major when airspace opacities disappear rapidly after
categories of disease that might lead to this the administration of diuretics, a different diagno-
identified pattern. sis is suggested than when these opacities would
In a second step, this list should be refined by remain unchanged or increase in size. Careful
trying to determine the exact location of these analysis of the patient data that are available also
abnormalities. The location of abnormalities includes the correlation with clinical, and patho-
should be as precise as possible and is performed logical and laboratory data. The knowledge that a
by deciding whether these abnormalities are focal patient is immunocompromised will often change
or diffuse, predominantly peripheral or central or the differential diagnosis list.
in the upper, middle or lower parts of the lung, Although a stepwise analysis of these three
whether the airspaces or the interstitium are elements can result in a diagnosis or a narrow
affected and if disease seems to be distributed differential diagnosis list, it is often not possible
along the blood vessels, the bronchi or the lym- to make a definitive diagnosis because one or
phatics. Combining the appearance pattern and more of the elements discussed are unclear or
the distribution pattern of the abnormalities can missing: patterns can overlap and can change
3 Appearance Pattern of Disease 23
over time, disease can show an aberrant locali- scopic level. Only then is a fruitful discussion
sation and distribution, additional findings can possible and are radiology and pathology
be misleading, previous examinations can be complimentary.
missing or clinical history may be nonspecific.
Nevertheless, even if a diagnosis cannot be
made, it should be possible to suggest additional 3 Appearance Pattern
(imaging or other) procedures that may lead to of Disease
the precise diagnosis.
Finally, it should be emphasised that checking Generally, CT findings can be classified into four
the quality of the examination is very important. large categories based on their appearance:
Incorrect positioning of the patient, insufficient
image collimation, the presence of life-supporting • Abnormalities associated with an increase in
devices and especially incorrect exposure param- lung density, i.e. increased lung attenuation
eters are often responsible for a reduction in • Abnormalities associated with a decrease in
image quality and for a possible misinterpreta- lung density, i.e. decreased lung attenuation
tion of the CT findings. • Abnormalities presenting as nodular opacities
• Abnormalities presenting as linear opacities