Respiratory system
Acute respiratory distress syndrome
Cyanide poisoning
Decompression sickness
Methemoglobinemia
Pulmonary changes at high altitude and altitude sickness
Congenital pulmonary airway malformation
Pulmonary hypoplasia
Tracheoesophageal fistula
Pneumonia
Lung cancer
Pancoast tumor
Superior vena cava syndrome
Apnea of prematurity
Meconium aspiration syndrome
Neonatal respiratory distress syndrome
Sudden infant death syndrome
Transient tachypnea of the newborn
Alpha 1-antitrypsin deficiency
Asthma
Bronchiectasis
Chronic bronchitis
Cystic fibrosis
Emphysema
Hypersensitivity pneumonitis
Idiopathic pulmonary fibrosis
Restrictive lung diseases
Sarcoidosis
Apnea, hypoventilation and pulmonary hypertension: Pathology review
Cystic fibrosis: Pathology review
Deep vein thrombosis and pulmonary embolism: Pathology review
Lung cancer and mesothelioma: Pathology review
Obstructive lung diseases: Pathology review
Pleural effusion, pneumothorax, hemothorax and atelectasis: Pathology review
Pneumonia: Pathology review
Respiratory distress syndrome: Pathology review
Restrictive lung diseases: Pathology review
Tuberculosis: Pathology review
Tracheoesophageal fistula
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Tracheoesophageal fistula (TEF) is a medical condition where there is an abnormal connection, or fistula, between the trachea (windpipe) and the esophagus (food pipe). In newborns, TEF occurs as a congenital birth defect caused by the failure of the trachea and esophagus to separate during fetal development. Symptoms of TEF include difficulty feeding, choking, coughing, and respiratory distress. In some cases, an infant may also develop aspiration pneumonia due to food or liquid entering the lungs through the fistula. Once diagnosed, prompt surgery is required to allow the food intake.
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