Pneumothorax is a medical emergency that requires immediate treatment due to its direct impact on respiratory function. Pneumothorax is easily recognized due to its sudden onset with symptoms of severe chest pain, dry cough, and difficulty breathing.

Spontaneous pneumothorax is a condition in which air suddenly appears in the pleural cavity without external causes such as trauma or injury.

Pneumothorax is a common respiratory disorder that occurs in many different diseases and can occur at any age. X-ray of pneumothorax is a method to help diagnose this condition.

Hemothorax-pneumothorax occurs in over 85% of blunt chest trauma. This is a serious condition, potentially life-threatening, requiring prompt emergency intervention.

Pneumothorax is a common condition that occurs when air enters the pleural cavity, leading to lung collapse due to increased pleural pressure. Patients with pneumothorax should have a thoracentesis performed as an initial treatment.

Pneumothorax occurs when air leaks between the lung and the chest wall, causing the lung on the affected side to collapse, reducing the ability to breathe.

Pneumothorax is a condition in which air accumulates between the lung and the chest wall. Air entering the pleural cavity can come from the lung or from outside the body. If not treated promptly, pneumothorax can lead to dangerous complications.

Pneumothorax is a pathology in which air accumulates in the pleural cavity, causing the lung to passively collapse, affecting the respiratory function of the body. Pneumothorax has many different causes as well as ways of diagnosis and treatment, depending on whether it is spontaneous pneumothorax or recurrent pneumothorax.

Congenital pulmonary airway malformation (CPAM), also known as congenital pulmonary cystic adenomatous malformation (CCAM), is a rare developmental abnormality of the lower respiratory tract. Infants with this malformation may present with respiratory distress in the neonatal period or may remain asymptomatic until late in life. Many cases are detected early by routine prenatal ultrasound. Surgical resection is the definitive treatment.

Congenital pulmonary airway malformation (CPAM), also known as congenital pulmonary cystic adenomatous malformation (CCAM), is a rare developmental abnormality of the lower respiratory tract. Infants with this malformation may present with respiratory distress in the neonatal period or may remain asymptomatic until late in life. Many cases are detected early by routine prenatal ultrasound. Surgical resection is the definitive treatment.