Spontaneous pneumomediastinum and subcutaneous emphysema after masturbation

Nikola Rajic1, Christian Schandl1

  • 1Center for Intensive Care, Kantonsspital Winterthur, Brauerstrasse 15, Winterthur 8401, Switzerland.

Radiology Case Reports
|March 29, 2022
PubMed

Insights

Spontaneous pneumomediastinum, a rare condition in young men, typically resolves on its own. This case details an unusual presentation linked to autoerotic activity, expanding understanding of this condition.

Area of Science:

  • Thoracic Medicine
  • Medical Case Reports
  • Pulmonology

Background:

  • Spontaneous pneumomediastinum (SPM) is a rare condition, often affecting young males, characterized by air in the mediastinum.
  • It typically arises from increased intrathoracic pressure due to activities like forceful coughing, vomiting, or strenuous exercise.
  • SPM usually follows a benign, self-limiting course, differentiating it from secondary causes like trauma or esophageal perforation.

Observation:

  • A healthy young male presented with spontaneous pneumomediastinum and extensive subcutaneous emphysema.
  • The onset of symptoms was associated with masturbation, an activity not previously documented as a trigger for SPM.
  • This presentation highlights an unusual association with autoerotic experiences.

Findings:

  • The case demonstrates spontaneous pneumomediastinum and significant subcutaneous emphysema.
  • The patient's condition developed during an autoerotic event, representing a novel trigger.
  • No underlying trauma or iatrogenic cause was identified.

Implications:

  • This case expands the spectrum of activities that can precipitate spontaneous pneumomediastinum.
  • It suggests that autoerotic activity, like other strenuous maneuvers, can lead to alveolar rupture and air dissection.
  • Further investigation may be warranted to understand the physiological mechanisms linking autoeroticism to SPM.

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