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Published on : Jul 28, 2021 | Views : 2507 | Downloads : 11

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DR SIDRA AFZAL PGR NEW RADIOLOGY DEPT. SIMS LAHORE PAEDIATRIC CHEST IMAGING
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The initial assessment of the pediatric CXR should include: Technique of the exam, to include patient positioning, proper exposure and the degree of inspiration Position of all tubes and lines and evaluation for pneumothorax, pneumomediastinum, and pneumoperitoneum Mediastinal and cardiac silhouettes Airway and lungs Pulmonary vascular pattern
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The initial assessment of the pediatric chest radiograph should include an evaluation of the degree of inspiration. It is difficult to obtain a full inspiratory film in the younger pediatric patient, and the radiologist should not confuse an expiratory film with pulmonary pathology Normal Inspiratory CXR Example of an Expiratory Exam
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Another important feature to recognize in the pediatric chest is the normal thymic tissue in the anterior mediastinum. Normal thymic tissue, as demonstrated on this image, should not be confused with a mediastinal or pulmonary mass
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Respiratory Neonatal Distress Excluding congenital heart disease, neonatal respiratory distress can be broken down into two broad categories: medical and surgical. Medical Causes of Neonatal Respiratory Distress Transient Tachypnea of the Newborn Meconium Aspiration Neonatal Pneumonia Respiratory Distress Syndrome (Surfactant Deficiency) Surgical Causes of Neonatal Respiratory Distress Congenital Diaphragmatic Hernia Congenital Cystic Adenomatoid Malformation Congenital Lobar Emphysema Sequestration
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1. Transient Tachypnea of the Newborn (TTN) Transient tachypnea of the newborn is delayed clearance of intrauterine pulmonary fluid. The infant has normal respiration during the first hours of life but then gradually develops mild respiratory distress which begins around 4-6 hours and peaks at 24 hours with rapid recovery by 48-72 hours The chest radiograph will follow the clinical course with the abnormalities peaking during the first day of life then rapidly clearing. The CXR will demonstrate the findings of fluid overload with vascular congestion and small pleural effusions. The CXR is nearly always normal by 48-72 hours. Medical Causes
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TTN on day one of life with mild vascular congestion and small pleural effusions On day two of life the fluid overload has resolved and the CXR is normal
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2. Neonatal Pneumonia Neonatal pneumonia can be a difficult clinical and radiographic diagnosis. Many different organisms can cause neonatal pneumonia but group B streptococcus is one of the most common infecting agents. Neonatal pneumonia can present with either diffuse reticulonodular densities similar to respiratory distress syndrome or with patchy, asymmetric infiltrates with hyperaeration similar to meconium aspiration. The presence of a small pleural effusion is a useful distinguishing feature as it is a common finding in neonatal pneumonia (up to 2/3) and is uncommon in respiratory distress syndrome.
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Example of neonatal pneumonia presenting as patchy, asymmetric opacities with a small right pleural effusion.
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3. Meconium Aspiration Syndrome Meconium staining of the amniotic fluid is relative common, affecting approximately 10% of live births, but only 1% will have meconium aspiration syndrome. The diagnosis is confirmed with visualization of meconium below the vocal cords. The radiology of meconium aspiration reflects the underlying pathophysiology. The aspirated meconium results in complete obstruction of the bronchi, resulting in atelectasis and compensatory hyperinflation of the remaining patent airways. Overall the lungs appear hyperinflated. Barotrauma is a frequent complication.
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CXR shows hyperinflation and patchy asymmetric airspace disease that is typical of meconium aspiration
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Respiratory distress syndrome is the term used to describe the clinical manifestations of surfactant deficiency, and it is synonymous with hyaline membrane disease (HMD). RDS is seen in children less than 36 weeks old and is obviously more prevalent and more severe the younger the premature infant. RDS presents immediately at birth with respiratory compromise. The classic radiographic findings of RDS include a) diffuse symmetric reticulogranular densities, a) prominent central air bronchograms and generalized hypoventilation. 4. Respiratory Distress Syndrome (RDS)
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CXR in a premature infant prior to intubation with severe hypoventilation, marked air bronchograms and diffuse symmetric reticulogranular opacities.
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Complications of Respiratory Distress The neonatologist must maintain a balance between the ventilatory needs of the infant and the complications that can result from positive pressure ventilation. The lung volumes on the daily neonatal CXR are used as a guide to determine the ventilator settings. If the compliance of the lungs is too low, or the mean airway pressure is too high, barotrauma will result. The signs of barotrauma should be identified on the neonatal CXR. Complications include, Pneumothorax PIE ( Pulmonary interstitial emphysema) Patent ductus arteriosus Chronic Lung Disease (CLD) and Bronchopulmonary Dysplasia (BPD)
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1. Pneumothorax Most exams in the neonate will be performed in the supine position, so the air will rise to the least dependent portion of the body. The least dependent portion of the chest is the anterior, lower chest. This is where we should look for a pneumothorax, which will appear as an unusually sharp heart border or an unusually sharp and lucent costophrenic angle on a supine CXR. The hyperlucent costophrenic angle is known as the deep sulcus sign.
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The following illustrates a case of a pneumothorax shown on supine CXR and confirmed by decubitis CXR, Supine CXR demonstrating a hyperlucent right heart border indicating a right anterior pneumothorax. Confirmed with a left decubitus chest x ray
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2. Pulmonary interstitial emphysema (PIE) Pulmonary interstitial emphysema (PIE) results from rupture of the alveoli with air accumulating in the peribronchial and perivascular spaces. PIE is recognized by linear lucencies radiating from the hilum. However, PIE can also be cystic in appearance, which can be difficult to distinguish from chronic lung disease. Correlation with the clinical course is helpful as PIE occurs early and is associated with high ventilatory settings, and chronic lung disease occurs later in the hospital course with lower ventilatory settings. PIE is an ominous sign because it indicates the poor compliance of the lungs and is frequently followed by a pneumothorax.
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Example of unilateral PIE with a pneumothorax Close up of left lung demonstrating the streaky lucencies of the air in the interstitium (red arrows) complicated by a pneumothorax (yellow arrow).
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3. Patent Ductus Arteriosus (PDA) The ductus is normally open in utero but will close in 1-2 days after birth in response to the decreased pulmonary resistance. If the pulmonary resistance remains high then the ductus may remain open with a right to left shunt. During the first week of life, as the ventilatory therapy decreases the pulmonary resistance, the ductus may switch to a left to right shunt resulting in increased pulmonary blood flow. This is demonstrated on CXR by increased heart size and increased pulmonary vascularity. An echo will confirm the PDA.
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CXR shows an enlarged heart and significant vascular congestion resulting from a PDA
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4. Chronic Lung Disease (CLD) Bronchopulmonary Dysplasia (BPD) Chronic lung disease and bronchopulmonary dysplasia are synonymous terms referring to the long-term sequelae of respiratory distress syndrome. Oxygen toxicity and positive pressure ventilation are thought to result in pulmonary inflammation with subsequent fibrosis. Clinically, CLD is defined as continued oxygen needs and CXR abnormalities beyond 28 days of life or 36 weeks gestational age. The radiographic manifestations of CLD are diffuse interstitial thickening with hyperinflation. The most severe form manifests in cystic changes in the lungs.
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Cystic interstitial pulmonary disease reflecting the severe form of chronic lung disease.
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Surgical Causes Congenital Diaphragmatic Hernia (CDH) A defect in the diaphragm will result in herniation of abdominal contents into the thoracic cavity. The mass effect from the abdominal contents in the chest will lead to severe respiratory distress from pulmonary hypoplasia in both the ipsilateral and contralateral lung. The most common defect is in the posterior and lateral diaphragm. This is a Bochdalek hernia, which is more common on the left (75%). A Morgagni hernia is less common and is anterior and medial. Morgagni hernias present later in life and are more common on the right because the heart and pericardium will protect the left side.
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Postnatal CXR demonstrates a mass in the lower left chest with shift of the mediastinum. The presence of bowel gas (red arrow) indicates the mass is due to a diaphragmatic hernia. In this case, the stomach remains in the abdominal cavity as indicated by the position of the nasogastric tube (yellow arrow) Another CXR demonstrates a mass in the left chest with shift of the mediastinum. Although no bowel gas is identified, the position of the nasogastric tube (red arrow) indicates the stomach is located in the thoracic cavity
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Congenital cystic adenomatoid malformation is a hamartoma of the lung. The presentation can vary from a large cystic lesion to a grossly solid appearing lesion that is composed of microscopic cysts. CCAM has a normal pulmonary arterial supply as opposed to pulmonary sequestration. Three types of CCAM are recognized depending on gross appearance: Type I CCAM - Most frequent (2/3 of cases), contains a dominant cyst > 2 cm surrounded by multiple, smaller cysts. Type II CCAM - (15-33%) uniform smaller cysts up to 2 cm. Other congenital malformations are associated with Type II CCAM in 50% of cases. Type III CCAM - Least common (< 10%), contains microscopic cysts that are not grossly visible. Grossly and on imaging the lesion appears solid. Fetal hydrops and maternal polyhydramnios are frequent complications. 2. Congenital cystic adenomatoid malformation
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Example of a Type 1 CCAM on CXR with a large dominant cyst containing an air fluid level
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Chest CT on the same patient confirms a Type I CCAM with a large dominant cyst surrounded by multiple smaller cysts
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3. Congenital Lobar Emphysema (CLE) Congenital lobar emphysema is characterized by overexpansion of one or more lobes. Emphysema is a misnomer as there is no destruction of alveoli. CLE is most common in left upper lobe. Initially, CLE will appear as a solid mass on both prenatal US and postnatal CXR because of the delayed clearance of pulmonary fluid. Over several days the fluid will slowly resorb, and the classic findings of a hyperlucent lobe will be present.
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Initial postnatal CXR demonstrates a solid appearing mass in the left upper chest (red arrows) with mass effect and shift of the mediastinum (yellow arrow). At this point, the CLE is filled with fluid and thus mimics a solid mass. Chest CT on day 2 of life. The fluid has been absorbed and the left upper lobe is shown to be hyperinflated resulting in mas effect and shift of the mediastinum.
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4. Pulmonary Sequestration Pulmonary sequestration is lung tissue that is not connected to the tracheobronchial tree. Sequestration has a systemic arterial supply instead of a pulmonary artery supply. The venous drainage can be either systemic or pulmonary. Two types of sequestration, intralobar and extralobar, are recognized. The most common location is the medial left lower lobe. Intralobar sequestration is contained within the normal lung pleura and presents in the 2nd or 3rd decades with recurrent infections. Extralobar sequestration is contained in its own separate pleura and commonly presents in the neonatal period with respiratory distress from mass effect. Furthermore, other anomalies are frequently found with extralobar sequestration.
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Intralobar sequestion in a 20 month old child . An ill-defined opacity in the right lower zone, adjacent to the right cardiac border, without silhouetting it, suggesting to be located in the left lower lobe. Which is confirmed on CT https://radiopaedia.org
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Axial contrast-enhanced CT scan through the lung bases with a large systemic vessel arising from the left side of the aorta supplying a very vascular left-sided extralobar sequestration (ELS) (arrow B) Corona) CT multiplanar reconstruction (MPR) showing the normal Lung and beneath this (arrow) the left-sided basal ELS with a draining vein entering the azygous system below the diaphragm david sutton
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Pulmonary Inflammatory Diseases in padiatrics 1. Viral Pulmonary Infections Respiratory syncytial virus (RSV) is the most frequently encountered viral agent in the infant and toddler population, usually presenting in the winter months. Viral infections tend to most severely affect the tracheobronchial tree, resulting in bronchiolitis and bronchitis, with relative sparing of the lung parenchyma. The role of the radiologist in interpreting a CXR in a patient with a respiratory infection is to determine if it is viral or bacterial. In summary, viral respiratory infections result in bronchitis, which manifests as peribronchial cuffing, dirty hilum and hyperinflation. Bacterial pneumonia will manifest as focal lobar consolidation with pleural effusion being common.
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Viral Pulmonary Infection - CXR Findings Bronchitis will manifest on the CXR as peribronchial thickening or "peribronchial cuffing". A bronchus seen on end will show the bronchial wall thickening, and the hilum will demonstrate a dirty appearance, which is well demonstrated on the lateral projection. The bronchial inflammation results in areas of mucus plugging and atelectasis whereas other areas of the lung will demonstrate hyperinflation from air trapping. The overall lung volumes will be hyperinflated with an increase in the anterior retrosternal space and flattening of the diaphragms. Viral infections do not have pleural effusions, however, these are relatively common in bacterial infections.
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Respiratory syncytial virus infection in a child. (a) Anteroposterior radiograph shows prominent peribronchial markings. (b) Patches of atelectasis (arrow) are best seen on lateral projection of the hyperinflated lungs. RSNA
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2. Bacterial Pulmonary Infection Neonatal pneumonia is frequently caused by group b streptococcus. The CXR findings are diagnostic of pneumonia but not specific as to the infecting organism. The most typical presentation is a lobar bronchopneumonia, which manifests on CXR as focal lobar consolidation with air bronchograms. The consolidation may have a round appearance, called "round pneumonia", which can mimic a pulmonary mass.
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Example of a right middle lobe pneumonia. PA and LAT CXR demonstrate consolidation in the right middle lobe.
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Example of a "round pneumonia." PA and LAT CXR shows a round opacity in the superior segment of the right lower lobe which has the appearance of a mass.
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Pneumatoceles are frequent with staphylococcal infections, and they should not be confused with a pulmonary abscess. Pneumatoceles have thin, smooth walls and are seen with an improving clinical picture, whereas pulmonary abscesses have thick, irregular walls with an air fluid level and the child tends to be very ill. Pneumatoceles are thought to be a form of localized pulmonary interstitial emphysema and are self limiting with only the rare case of a large, persisting pneumatocele needing surgery. consolidation. Initial CXR shows a dense right upper lobe CXR a week later shows a round cyst with thin walls in the right upper lobe.
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Primary TB in the pediatric population differs from the presentation of reactivation TB seen in adults. Primary TB produces a focal lobar consolidation in any pulmonary lobe. Hilar adenopathy and pleural effusions are common and should alert the radiologist to the possibility of TB. If the lungs are secondarily infected hematogenously, miliary TB will result and present as characteristic, uniform small nodules diffusely through the lungs. 3. Tuberculosis
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PA and LAT CXR with diffuse air space disease throughout the right upper lobe and significant right paratracheal adenopathy. The red arrow indicates adenopathy; the yellow arrow indicates TB pneumonia.
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Miliary tuberculosis. Fine nodularity throughout both lungs david sutton
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4. Cystic Fibrosis (CF) Cystic Fibrosis is an autosomal recessive disease affecting 1/1500 caucasian individuals. The pulmonary system is most severely affected, but gastrointestinal complications are also common with meconium ileus in the newborn period and malabsorption that can result in failure to thrive The presence of multiple recurrent pulmonary infections should lead to a test for CF. Eventually, the CXR will demonstrate the characteristic hyperinflation and bronchiectasis. The CXR is used primarily to monitor acute infections and the general progression of the disease.
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Extensive central bronchiectasis with secondary infection in a 12 yr old male child with cystic fibrosis https://radiopaedia.org/
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Advanced cystic fibrosis (mucoviscidosis). Gross peribronchial shadowing with confluent pneumonic shadowing. There is a left pneumothorax with slight displacement of the mediastinum to the right david sutton
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Advanced cystic fibrosis on coronal CT image Bilateral severe, widespread bronchiectasis with occasional mucus plugging and background mosaic attenuation, most likely due to air trapping. Lung volumes are increased https://radiopaedia.org/
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PULMONARY UNDERDEVELOPMENT Pulmonary underdevelopment including absent lung is fairly common. The three types of pulmonary underdevelopment are age- nesis, aplasia and hypoplasia. Agenesis is complete absence of a lung or lobe with absent bronchi Aplasia is absence of lung tissue but the pres- ence of a rudimentary bronchus, and Hypoplasia is the presence of both bronchi and alveoli in an underdeveloped lobe
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Lung agenesis Complete agenesis is easily recognisable with a small opaque hemithorax and displacement of mediastinal structures towards that side. Right lung agenesis has a higher mortality rate, possibly because of the higher incidence of cardiovascular abnormalities. Chest X-ray showing overinflated left lung in a neonate with crowding of the ribs and opacification of the right hemithorax due to agenesis of the right lung david sutton
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Lobar underdevelopment or Pulmonary hypoplasia is caused by factors directly or indirectly compromising the thoracic space available for lung growth. These factors may be intrathoracic (diaphragmatic hernia, extralobar sequestration) or extrathoracic (oligohydramnios) With lung hypoplasia there is a decrease in volume of the hemithorax, with an increased density of tissues and displacement of the heart and mediastinum towards the abnormal side. Associated abnormalities are diaphragmatic hernia and renal dysgenesis/agenesis
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Chest X-ray showing hypoplasia of the right lung with mediastinal shift to the right. VQ scans show reduced ventilation and perfusion to the abnormal hypoplastic right lung (posterior view david sutton
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Congenital pulmonary venolobar syndrome THE abnormalities include: anomalous pulmonary venous drainage particularly scimitar syndrome with hypogenetic right lung pulmonary sequestration with systemic pulmonary vascular supply horseshoe lung Scimitar syndrome, also known as hypogenetic lung syndrome, is characterised by a hypoplastic lung that is drained by an anomalous vein into the systemic venous system. It is a type of partial anomalous pulmonary venous return and is one of several findings in congenital pulmonary venolobar syndrome.
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The x-ray also shows right lung hypoplasia (under-development) and the scimitar vein which reminds the curved Turkish sword that carries that name
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Scimitar syndrome, The right lung is grossly smaller than the left and the mediastinum is shifted to the right. An anomalous pulmonary vein that drains directly into the inferior vena cava. https://radiopaedia.org/
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