Revista médica de Chile
versión impresa ISSN 0034-9887
ALVAREZ Z, Carlos et al. Spontaneous pneumomediastinum: Review of eight cases. Rev. méd. Chile [online]. 2009, vol.137, n.8, pp. 1045-1050. ISSN 0034-9887. http://dx.doi.org/10.4067/S0034-98872009000800007.
Background: Hamman syndrome or spontaneous pneumomediastinum is uncommon and its clinical manifestations are chest pain, dyspnea and subcutaneous emphysema. Aim: To report a series of patients with spontaneous pneumomediastinum. Material and methods: Medical records of patients with the diagnosis of pneumomediastinum, managed between 2002 and 2007 in a public hospital, were retrieved and reviewed. Results: Eight patients aged between 16 and 41 years (five males) were identified. The most common symptom was chest pain and the most common sign was subcutaneous emphysema. A chest X ray was performed in all and a chest CT scan in seven. AH were managed conservatively with oxygen, analgesia and rest. No patient required surgery and the evolution was favorable. Conclusions: The most common presenting complaint of spontaneous pneumomediastinum is chest pain and its management does not require surgery.
Palabras clave : Chest pain; Mediastinal emphysema; Subcutaneous emphysema.