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Case Reports
. 2015 Sep 21:2015:bcr2015209750.
doi: 10.1136/bcr-2015-209750.

Recreational nitrous oxide inhalation as a rare cause of spontaneous pneumomediastinum

Affiliations
Case Reports

Recreational nitrous oxide inhalation as a rare cause of spontaneous pneumomediastinum

Rory McDermott et al. BMJ Case Rep. .

Abstract

A 17-year-old girl presented to the A&E department with significant neck swelling with associated chest, neck and throat pain. She reported recreational inhalation of nitrous oxide and ingestion of MDMA (3,4-methylenedioxy-methamphetamine) in the preceding hours. There was no history of trauma or vomiting. Clinical examination revealed extensive subcutaneous emphysema. There was no airway compromise. A chest X-ray suggested the presence of a pneumomediastinum. Subsequent CT of the thorax confirmed an anterior pneumothorax and a pneumopericardium. The patient was admitted for observation and intravenous antibiotics. Further investigations ruled out an oesophageal perforation. The patient was discharged following a period of clinical stability and has since made an uneventful recovery. MDMA ingestion has been cited as a rare cause of spontaneous pneumomediastinum in a series of case reports. In this case, it is likely that the inhalation of nitrous oxide contributed to the development and expansion of a pneumomediastinum.

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Figures

Figure 1
Figure 1
Chest radiograph revealing a double left-sided cardiac border indicating the presence of air in the mediastinum.
Figure 2
Figure 2
CT of the thorax demonstrating subcutaneous emphysema and air dissecting the fascial planes.
Figure 3
Figure 3
CT of the thorax confirming the presence of an anterior pneumothorax and a pneumopericardium.
Figure 4
Figure 4
CT of the thorax confirming the presence of an anterior pneumothorax and a pneumopericardium.

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