Hamman's syndrome

Hamman's Syndrome is a rare condition characterized by spontaneous subcutaneous emphysema and pneumomediastinum. It is also known as spontaneous pneumomediastinum. The condition is named after Louis Hamman, an American physician who first described the syndrome in 1939.

Symptoms

The most common symptoms of Hamman's Syndrome include chest pain, dyspnea (shortness of breath), and subcutaneous emphysema, which is characterized by a crackling sensation upon touching the skin. Other symptoms may include cough, neck pain, dysphagia (difficulty swallowing), and hoarseness.

Causes

Hamman's Syndrome is typically caused by activities that lead to a sudden increase in intrathoracic pressure, such as coughing, vomiting, childbirth, or strenuous exercise. It can also occur as a complication of certain medical procedures, such as bronchoscopy or mechanical ventilation.

Diagnosis

The diagnosis of Hamman's Syndrome is usually made based on the patient's symptoms and physical examination findings. Imaging studies, such as chest X-ray or computed tomography (CT) scan, may also be used to confirm the diagnosis.

Treatment

The treatment of Hamman's Syndrome is primarily supportive, as the condition usually resolves on its own without specific treatment. Pain relief and oxygen therapy may be provided to manage symptoms. In severe cases, surgical intervention may be required.

See Also

• Subcutaneous emphysema
• Pneumomediastinum
• Louis Hamman

References

Hamman's syndrome Resources
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