Part 1 The clinical anatomy of the thorax, together with the anatomy of radiological and other imaging techniques of the thorax are in daily use in clinical practice. The routine clinical examination of the patient’s chest is little more than an exercise in relating the deep structures of the thorax to the chest wall. Moreover, several commonly undertaken procedures – chest aspiration, insertion of a chest drain or of a subclavian line, placement of a cardiac pacemaker, for example – have their basis, and their safe performance, in sound anatomical knowledge. Much of the working life of an experienced clinician is spent in relating the patient’s surface anatomy to underlying deep structures (Fig. 1; see also Figs 11, 22). The following bony prominences can usually be palpated in the living subject (corresponding vertebral levels are given in brackets): Note from Fig. 1 that the manubrium sterni corresponds to the 3rd and 4th thoracic vertebrae and overlies the aortic arch, and that the body of the sternum corresponds to the 5th–8th vertebrae and neatly overlies the heart. Since the 1st and 12th ribs are difficult to feel, the ribs should be enumerated from the 2nd costal cartilage, which articulates with the sternum at the angle of Louis. The spinous processes of all the thoracic vertebrae can be palpated in the midline posteriorly, but it should be remembered that the first spinous process that can be felt is that of C7 (the vertebra prominens). The position of the nipple varies considerably in the female, but in the male it usually overlies the 4th intercostal space approximately 10 cm (4 in) from the midline. The apex beat, which marks the lowest and outermost point at which the cardiac impulse can be palpated, is normally in the 5th intercostal space 9 cm (3.5 in) from the midline and within the midclavicular line. (This corresponds to just below and medial to the nipple in the male, but it is always preferable to use bony rather than soft‐tissue points of reference.) The trachea is palpable in the suprasternal notch midway between the heads of the two clavicles. The trachea commences in the neck at the level of the lower border of the cricoid cartilage (C6) and runs vertically downwards to end below the level of the sternal angle of Louis (T4/5), just to the right of the midline, by dividing to form the right and left main bronchi. In the erect position and in full inspiration the level of bifurcation is at T6. The cervical pleura can be marked out on the surface by a curved line drawn from the sternoclavicular joint to the junction of the medial and middle thirds of the clavicle; the apex of the pleura is approximately 2.5 cm (1 in) above the clavicle. This fact is easily explained by the oblique slope of the first rib. It is important because the pleura can be wounded (with consequent pneumothorax) by a stab wound – and this includes the surgeon’s knife and the anaesthetist’s needle – above the clavicle, or, in an attempted subclavian vein catheterization, below the clavicle. The lines of pleural reflexion pass from behind the sternoclavicular joint on each side to meet in the midline at the 2nd costal cartilage (the angle of Louis). The right pleural edge then passes vertically downwards to the 6th costal cartilage and then crosses: On the left side the pleural edge arches laterally at the 4th costal cartilage and descends lateral to the border of the sternum, owing, of course, to its lateral displacement by the heart; apart from this, its relationships are those of the right side. The pleura actually descends just below the 12th rib margin at its medial extremity – or even below the edge of the 11th rib if the 12th is unusually short; obviously, in this situation, the pleura may be opened accidentally in making a loin incision to expose the kidney, perform an adrenalectomy or drain a subphrenic abscess. The surface projection of the lung is somewhat less extensive than that of the parietal pleura as outlined previously, and in addition it varies quite considerably with the phase of respiration. The apex of the lung closely follows the line of the cervical pleura and the surface marking of the anterior border of the right lung corresponds to that of the right mediastinal pleura. On the left side, however, the anterior border has a distinct notch (the cardiac notch) that passes behind the 5th and 6th costal cartilages. The lower border of the lung has an excursion of as much as 5–8 cm (2–3 in) in the extremes of respiration, but in the neutral position (midway between inspiration and expiration) it lies along a line which crosses the 6th rib in the midclavicular line, the 8th rib in the midaxillary line and reaches the 10th rib adjacent to the vertebral column posteriorly. The oblique fissure, which divides the lung into upper and lower lobes, is indicated on the surface by a line drawn obliquely downwards and outwards from 2.5 cm (1 in) lateral to the spine of the 3rd thoracic vertebra along the 5th intercostal space to the 6th costal cartilage approximately 4 cm (1.5 in) from the midline. This can be represented approximately by abducting the shoulder to its full extent; the line of the oblique fissure then corresponds to the position of the medial border of the scapula. The surface markings of the transverse fissure (separating the middle and upper lobes of the right lung) is a line drawn horizontally along the 4th costal cartilage and meeting the oblique fissure where the latter crosses the 5th rib. The outline of the heart can be represented on the surface by an irregular quadrangle bounded by the following four points (Fig. 4): The left border of the heart (indicated by the curved line joining points 1 and 4) is formed almost entirely by the left ventricle (the auricular appendage of the left atrium peeping around this border superiorly); the lower border (the horizontal line joining points 3 and 4) corresponds to the right ventricle and the apical part of the left ventricle; the right border (marked by the line joining points 2 and 3) is formed by the right atrium (see Fig. 24a). A good guide to the size and position of your own heart is given by placing your clenched right fist palmar surface inwards immediately inferior to the manubriosternal junction. Note that the heart is approximately the size of the subject’s fist, lies behind the body of the sternum (therefore anterior to thoracic vertebrae 5–8) and bulges over to the left side. The surface markings of the vessels of the thoracic wall are of importance if these structures are to be avoided when performing aspiration of the chest. The internal thoracic (internal mammary) vessels run vertically downwards behind the costal cartilages 1.25 cm (0.5 in) from the lateral border of the sternum. The intercostal vessels lie immediately below their corresponding ribs (the vein above the artery) so that it is safe to pass a needle immediately above a rib, but hazardous to pass it immediately below (see Fig. 8). The thoracic cage is formed by the vertebral column behind, the ribs and intercostal spaces on either side and the sternum and costal cartilages in front. Above, it communicates through the superior aperture of the thoracic cage with the root of the neck; below, it is separated from the abdominal cavity by the diaphragm (Fig. 1). Amusingly, the superior aperture of the thoracic cage is termed the ‘thoracic inlet’ by anatomists, while clinicians (especially vascular surgeons, neurosurgeons and radiologists) refer to the same aperture as the ‘thoracic outlet’. See ‘The vertebral column’, page 347. See also page 350 and Fig. 228. The greater part of the thoracic cage is formed by the twelve pairs of ribs. Of these, the first seven are connected anteriorly by way of their costal cartilages to the sternum, the cartilages of the 8th, 9th and 10th articulate each with the cartilage of the rib above and the last two ribs are free anteriorly (‘floating ribs’). Each typical rib (Fig. 5) has a head bearing two articular facets, for articulation with the upper demifacet on the side of the body of the numerically corresponding thoracic vertebra and the lower demifacet of the vertebra above (see Fig. 228). Thus, the head of the third rib articulates with its own third vertebral body and the one above. The head continues as a stout neck, which gives attachment to the costotransverse ligaments, a tubercle with a rough non‐articular portion and a smooth facet, for articulation with the transverse process of the corresponding vertebra, and a long shaft flattened from side to side and divided into two parts by the ‘angle’ of the rib. The angle demarcates the lateral limit of attachment of the erector spinae muscle. The following are the significant features of the ‘atypical’ ribs. The 1st rib (Fig. 6) is flattened from above downwards. It is not only the flattest but also the shortest and most highly curved of all the ribs. It has a prominent tubercle on the inner border of its upper surface for the insertion of scalenus anterior. In front of this tubercle, the subclavian vein crosses the rib; behind the tubercle is the subclavian groove, where the subclavian artery and lowest trunk of the brachial plexus lie in relation to the bone. This is one of the sites where the anaesthetist can infiltrate the plexus with local anaesthetic. Crossing the front of the neck of the first rib vertically and lying from medial to lateral are the sympathetic trunk, the superior intercostal artery (from the costocervical trunk) and the large branch of the first thoracic nerve to the brachial plexus. The 2nd rib is much less curved than the 1st and approximately twice as long. The 10th rib has only one articular facet on the head. The 11th and 12th ribs (the ‘floating ribs’) are short, have no tubercles and only a single facet on the head. The 11th rib has a slight angle and a shallow subcostal groove; the 12th has neither of these features. These bars of hyaline cartilage serve to connect the upper seven ribs directly to the side of the sternum and the 8th, 9th and 10th ribs to the cartilage immediately above. The cartilages of the 11th and 12th ribs merely join the tapered extremities of these ribs and end in the abdominal musculature. This dagger‐shaped bone, which forms the anterior part of the thoracic cage, consists of three parts. The manubrium is roughly triangular in outline and provides articulation for the clavicles and for the first and upper part of the 2nd costal cartilages on either side. It is situated opposite the 3rd and 4th thoracic vertebrae. Opposite the disc between T4 and T5 it articulates at an oblique angle at the manubriosternal joint (the angle of Louis) with the body of the sternum (placed opposite T5–T8). This is composed of four parts or ‘sternebrae’, which fuse between puberty and 25 years of age. Its lateral border is notched to receive part of the 2nd and the 3rd to the 7th costal cartilages. The xiphoid process is the smallest part of the sternum and usually remains cartilaginous well into adult life. The cartilaginous manubriosternal joint and that between the xiphoid and the body of the sternum may also become ossified after the age of 30. There are slight variations between the different intercostal spaces, but typically each space contains three muscles, comparable to those of the abdominal wall, and an associated neurovascular bundle (Fig. 8). The muscles are: Just as in the abdomen, the nerves and vessels of the thoracic wall lie between the middle and innermost layers of muscles. This neurovascular bundle consists, from above downwards, of vein, artery and nerve, the vein lying in a groove on the undersurface of the corresponding rib (remember: v,a,n). The vessels comprise the posterior and anterior intercostal arteries and veins. The posterior intercostal arteries of the lower nine spaces are direct branches of the descending thoracic aorta, while the first two are derived from the superior intercostal branch of the costocervical trunk, the only branch of the second part of the subclavian artery. Each runs forward in the subcostal groove to anastomose with the anterior intercostal artery. Each has a number of branches to adjacent muscles, to the skin and to the spinal cord. The corresponding veins are mostly tributaries of the azygos and hemiazygos veins. The first posterior intercostal vein drains into the brachiocephalic or vertebral vein. On the left, the 2nd and 3rd veins often join to form a superior intercostal vein, which crosses the aortic arch to drain into the left brachiocephalic vein. The anterior intercostal arteries are branches of the internal thoracic artery (1st–6th space) or of its musculophrenic branch (7th–9th spaces). The lowest two spaces have only posterior arteries. Perforating branches pierce the upper five or six intercostal spaces; those of the 2nd–4th spaces are large in the female and supply the breast. The intercostal nerves are the anterior primary rami of the thoracic nerves, each of which gives off a collateral muscular branch and lateral and anterior cutaneous branches for the innervation of the thoracic and abdominal walls (Fig. 9). The diaphragm is the dome‐shaped septum dividing the thoracic from the abdominal cavity. It is present only in mammals. It comprises two portions: a peripheral muscular part that arises from the margins of the inferior aperture of the thoracic cage (termed by anatomists as the ‘thoracic outlet’) and a centrally placed aponeurosis (Fig. 10). The muscular fibres are arranged in three parts: The central tendon, into which the muscular fibres are inserted, is trefoil in shape and is partially fused with the undersurface of the pericardium. The diaphragm receives its entire motor supply from the phrenic nerve (C3, C4, C5), whose long course from the neck follows the embryological migration of the muscle of the diaphragm from the cervical region (see ‘The development of the diaphragm and the anatomy of diaphragmatic herniae’). Injury or operative transection of this nerve results in paralysis and permanent elevation of the ipsilateral half of the diaphragm. Radiographically, paralysis of the diaphragm is recognized by its elevation and paradoxical movement; instead of descending on inspiration, it is forced upwards by pressure from the abdominal viscera. The sensory nerve fibres from the central part of the diaphragm also run in the phrenic nerve; hence, irritation of the diaphragmatic pleura (in pleurisy) or of the peritoneum on the undersurface of the diaphragm by subphrenic collections of pus or blood produces referred pain in the corresponding cutaneous area, the shoulder‐tip. The peripheral part of the diaphragm, including the crura, receives sensory (proprioceptive) fibres from the lower intercostal nerves. The three main openings in the diaphragm (Figs 10, 11) are: In addition to these structures, the greater and lesser splanchnic nerves (see page 52) pierce the crura and the sympathetic chain passes behind the diaphragm deep to the medial arcuate ligament to reach the posterior abdominal wall. The diaphragm is formed (Fig. 12) by fusion in the embryo of: The septum transversum is the mesoderm which, in early development, lies in front of the head end of the embryo. With the folding off of the head, this mesodermal mass is carried ventrally and caudally, to lie in its definitive position at the anterior part of the diaphragm. During this migration, the cervical myotomes and nerves contribute muscle and nerve supply respectively, thus accounting for the long course of the phrenic nerve (C3, C4 and C5) from the neck to the diaphragm. With such a complex embryological story, one may be surprised to know that congenital abnormalities of the diaphragm are unusual. However, a number of defects can occur, giving rise to a variety of congenital herniae through the diaphragm. These may be: Far more common are the acquired hiatus herniae (subdivided into sliding and rolling herniae). These are found in patients usually of middle age in whom weakening and widening of the oesophageal hiatus has occurred (Fig. 13). In the sliding hernia the upper stomach and lower oesophagus slide upwards into the chest through the lax hiatus when the patient lies down or bends over; the competence of the cardia is often disturbed and peptic juice can therefore regurgitate into the gullet in lying down or bending over. This may be followed by oesophagitis with consequent heartburn, bleeding and, eventually, stricture formation. In the rolling hernia (which is far less common) the cardia remains in its normal position and the cardio‐oesophageal junction is intact, but the fundus of the stomach rolls up through the hiatus in front of the oesophagus; hence, the alternative term of para‐oesophageal hernia. In such a case there may be epigastric discomfort, flatulence and even dysphagia, but no regurgitation because the cardiac mechanism is undisturbed. During inspiration the movements of the chest wall and diaphragm result in an increase in all diameters of the thorax. This, in turn, brings about an increase in the negative intrapleural pressure and an expansion of the lung tissue. Conversely, in expiration the relaxation of the respiratory muscles and the elastic recoil of the lung reduce the thoracic capacity and force air out of the lungs. Quiet inspiration is brought about almost entirely by active contraction of the diaphragm with very little chest movement. Confirm this on yourself; your hands on your chest will show minimal movement as you breathe quietly. As respiratory movement grows deeper, the contraction of the intercostal muscles raises the ribs. The first rib remains relatively stationary, ribs 2–6 principally increase the anteroposterior diameter of the thorax (the pump handle movement), while the corresponding action of the lower ribs is to increase the transverse diameter of the thoracic cage (the bucket handle movement). Again, confirm this on your own chest during deep inspiration. In progressively deeper inspiration, more and more of the diaphragmatic musculature is called into play. On radiographic screening of the chest, the diaphragm will be seen to move approximately 2.5 cm (1 in) in quiet inspiration and up to 6–10 cm (2.5–4 in) on deep inspiration. Normal quiet expiration is brought about by elastic recoil of the elevated ribs and passive relaxation of the contracted diaphragm. In deeper expiration, the abdominal muscles have an important part to play – they contract vigorously, compress the abdominal viscera, raise the intra‐abdominal pressure and force the relaxed diaphragm upwards. Indeed, diaphragmatic movement accounts for approximately 65% of air exchange whereas chest movement accounts for the remaining 35%. In deep and forced inspiration, additional ‘accessory muscles of respiration’ are called into play. These are the muscles attached to the thorax that are normally used in movements of the arms and the head. Watch an athlete at the end of a run, or observe a severely dyspnoeic patient – he grips his thighs or the table to keep his arms still, holds his head stiffly and uses pectoralis major, serratus anterior, latissimus dorsi and sternocleidomastoid to act ‘from insertions to origins’ to increase the capacity of the thorax. Observe also that the woman in advanced pregnancy has her diaphragm elevated and splinted by the enlarged fetus – she relies on chest movements in respiration even when she is resting quietly as she sits in the antenatal clinic. The two pleural cavities are totally separate from each other (Fig. 2). Each pleura consists of two layers: a visceral layer intimately related to the surface of the lung, and a parietal layer lining the inner aspect of the chest wall, the upper surface of the diaphragm and the sides of the pericardium and mediastinum. The visceral layer is firmly attached to the underlying lung. In contrast, the parietal pleura is separated from its overlying structures by a loose, thin layer of connective tissue, the extrapleural fascia, which enables the surgeon to strip the parietal pleura easily from the chest wall. The two layers are continuous in front and behind the root of the lung, but below this the pleura hangs down in a loose fold, the pulmonary ligament, which forms a ‘dead space’ for distension of the pulmonary veins. The surface markings of the pleura and lungs have already been described in the section on surface anatomy. Notice that the lungs do not occupy all the available space in the pleural cavity, even in forced inspiration.
The Thorax
Introduction
Surface anatomy and surface markings
The trachea (Figs 1, 2)
The pleura (Figs 2, 3)
The lungs (Figs 2, 3)
The heart (Fig. 4)
The thoracic cage
The thoracic vertebrae
The ribs
The costal cartilages
The sternum
The intercostal spaces
The diaphragm
Openings in the diaphragm
The development of the diaphragm and the anatomy of diaphragmatic herniae
The movements of respiration
The pleurae