Thorax: Pleura and Diaphragms
Clear lung edge visible with thin pleural line.
Erect or semierect.
Clear lung edge visible with thin pleural line.
Usually erect film.
Lucency mirrors diaphragmatic surface, often with deep costophrenic sulcus. Lung edge and pleural line not necessarily visible.
Common patterns in neonates and infants in intensive care unit.
Crisply defined heart border with lucent area adjacent. Lung edge and pleural line not necessarily visible.
Fig. 1.67, p. 44
Diaphragmatic eversion and contralateral mediastinal displacement.
Requires emergency needle thoracotomy.
Air-fluid level with horizontal interface on horizontal beam film.
Most commonly due to overlying skin fold. No pleural line visible. Interface between densities may fade out or extend beyond the chest wall.
Repeat film with corrected rotation may be required.
Often preceded by or coexisting with pulmonary interstitial emphysema.
Common in ventilated neonates, particularly those with HMD and meconium aspiration syndrome. Hypoplastic lungs are also prone to barotrauma.
Iatrogenic, penetrating injury, blunt trauma to chest.
Evidence of underlying disease (e.g., peribronchial thickening). Blebs/bullae rarely visualized.
Particularly CF and asthma: rupture of blebs and bullae, or overdistended acini in areas of air trapping. In CF, lung may not collapse completely owing to reduced compliance.
Cavitating pneumonia occasionally spreads to pleural space. Often complicated by bronchopleural fistula.
Particularly with TB.
Interstitial lung disease
Evidence of underlying disease. Usually cystic change or established fibrosis present.
In children, LCH is the most common interstitial lung disease to cause pneumothorax.
Subpleural pulmonary metastases.
Usually sarcoma, particularly osteosarcoma.
Normal underlying lungs: very occasionally visualize bleb.
Rare in young children. Typically in tall athletic males. Occasionally in Marfan syndrome.
Fig. 1.80, p. 52
Parallels chest wall. Common pattern in children.
Fig. 1.7, p. 8
May simulate mass. Lateral radiograph often confirms position in fissure.
Medially convex collection produces lentiform shape, may simulate pulmonary abscess. Fluid does not shift with change of posture.
Usually in empyema or occasionally hemothorax.
Diaphragm appears to be peaked laterally. US used to confirm.
Usually due to skin fold from overlying arm.
Underlying lung consolidation. US may show minor septation or simple anechoic effusion.
Distinction from empyema frequently requires aspiration.
Difficult to distinguish from simple parapneumonic effusion on radiograph. May be lobulated.
US: echoic fluid, thin or thick septations or even solid appearing collection.
CT: pleural enhancement, thickening of extrapleural fat, lobulated appearing collection.
Commonly following streptococcal or staphylococcal pneumonia. Incidence may be rising in children. Treated with either tube thoracostomy with fibrinolytics or surgically (usually video-assisted thoracoscopy).
Primary complex often not visible.
Rare prior to school age. Ten percent of primary TB.
CXR: may visualize lobulated pleural mass.
CT: irregular/nodular pleural thickening.
Common causes: leukemia/lymphoma. Metastatic disease particularly Wilms tumor, and sarcoma, primary tumors including PNET, Askin disease, mesothelioma.
May be evidence of lymphangiectasia.
Fluid milky after feeding. May be idiopathic, secondary to lymphatic injury (e.g., birth trauma, cardiac surgery), or associated with lymphangiectasia.
Usually left-sided and small.
Usually small, sympathetic effusion.
Often larger on the right.
In low albumin states, cardiac failure, “third spacing” in sepsis.
Hyperdense on CT examination: density measures 30–80 Hounsfield units (HU) depending on age of blood.
Usually following trauma or iatrogenic.
“Rind” of pleural thickening along lateral margin.
Associated rib lesion
Fig. 1.38, p. 28
Fracture or neoplasm (primary lesions: PNET, Askin tumor).
Solid pleural thickening.
Leukemia, neuroblastoma, and Wilms tumor most common primary lesions.
Ipsilateral pulmonary vascular anomaly
Pleural companion shadows due to collateral vessels in pleural space. Occurs in pulmonary artery or vein atresia.
Primary pleural neoplasm
Lipoma: fat density areas.
Liposarcoma: nonspecific infiltrative mass.
Mesothelioma: Not asbestos-related: occasionally following radiotherapy. Similar to adult form.
Fig. 1.61, p. 41
More commonly left-sided. Usually contains bowel ± solid viscera. NG tube and umbilical catheters may deviate toward defect. Gas in hernia in continuity with abdominal bowel gas, which is sparse. Compresses ipsi-lateral ± contralateral lung, resulting in hypoplasia.
Large defects almost invariably presenting in neonatal period.
Predominantly right-sided (10:1). Hepatic lobe (s), stomach, duodenum, small and large bowel, as well as spleen and omentum may all herniate. Chest and abdomen radiograph: soft-tissue density projected over the costophrenic and cardiophrenic angles. Lateral view: only the posterior portion of the diaphragm is discernable, the hernia is retrosternal density. The plain radiograph is often sufficient, especially when the hernia contains aerated bowel. US, possibly CT. Scintigraphy if hemorrhaging.
Rare approximately 7% of congenital hernias; very rarely bilateral. Early childhood, adulthood. Associated anomalies: scimitar syndrome, unilobar lungs, Hirschsprung disease. Complications: incarceration, gastric volvulus. Many are asymptomatic.
May be sliding or rolling.
May be component of Bochdalek hernia.
Fig. 1.86a, b, p. 56
More commonly right sided. Diaphragm shows reduced excursion and lobulated contour with upward displacement.
Due to a congenitally thin diaphragm. Unilateral associated with trisomies 13, 15, and 18, and Beckwith-Wiedemann syndrome. Bilateral in congenital CMV infection and toxoplasmosis.
Widening of the esophageal hiatus. Central supradiaphragmatic hernia, mainly consisting of a small section of the cardia, varying from a small nubbin to several centimeters. Lateral view: middle mediastinum. Sliding hernia seen only in inspiration. Gastroesophageal overdistention may be required to demonstrate gastroesophageal reflux. Danger of reflux esophagitis, even peptic esophageal stricture. US, endoscopy.
Gastroesophageal reflux and vomiting from birth, failure to thrive, iron deficiency anemia, melena, and hematemesis indicate reflux esophagitis. Infants are most commonly affected.
Fig. 1.87, p. 56
Cardia in normal position part of stomach herniates alongside the esophagus through the esophageal hiatus. Right more common than left. Plain radiograph: circular “cyst” in the cardiophrenic angle. Lateral view: central in position. Confirmation with a contrast study.
Mainly in older infants and school age children. Seldom symptoms, occasionally vomiting.
Bochdalek hernia (lumbocostal and pleuroperitoneal canals)
Fig. 1.88a, b, p. 56
Mnemonic: BBBB, Bochdalek, Back, Big, Babies
Bochdalek hernia: larger neonatal diaphragmatic defect
Predominantly left-sided. Herniation of stomach, spleen, and bowel; liver when right-sided. Kidney position high. The hemithorax is initially dense after birth, becoming cystic or honeycombed when the bowel fills with air. The diaphragm is not identified. Mediastinum deviated to the contralateral side. Small scaphoid abdomen with no air, absent liver shadow. US (prenatal and postnatal).
Most common true diaphragmatic defect, rarely with a hernial sac. Severe illness. Decisive for the prognosis: degree of ipsilateral and contralateral pulmonary hypoplasia. Commonly associated with other anomalies (cardiovascular, malrotation, skeletal, etc). Requires immediate surgical repair and/or ECMO until the lungs mature. Prognosis: still only 45% survival rate.
Bochdalek hernia: less severe forms, diagnosed later
Left more common than right. Dense homogeneous or cystic honeycombing appearance caused by air-containing bowel loops. Lateral view posterolateral herniation.
In neonates or in older infants. Milder clinical symptoms than with the larger defect, occasionally even an incidental finding. Associated with other anomalies.
Bochdalek hernia: late type, delayed presentation
Radiographic findings only after the first or second week of life, occasionally even later. Initially normal chest radiograph, with sudden onset of density and mediastinal shift. When right-sided: “absent liver” sign, as the liver is displaced into the thorax, and air-containing bowel loops fill the right upper quadrant of the abdomen.
Origin is unclear; it is thought that the liver and spleen prevent hermiation in infancy. Clinical symptoms occur simultaneously with the radiographic changes.