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Pneumatosis cystoides intestinalis with free intraperitoneal air: a case report

Joanna Hwang1, V Sreenath Reddy, Kenneth W Sharp

  • 1Division of General Surgery, Vanderbilt University Medical Center, Nashville, Tennessee 37232-2577, USA.

The American Surgeon
|April 29, 2003
PubMed

Insights

Pneumatosis cystoides intestinalis (PCI) is a rare condition. This case shows that free air on imaging does not always require surgery for PCI, with supportive care being effective.

Area of Science:

  • Gastroenterology
  • Radiology
  • Internal Medicine

Background:

  • Pneumatosis cystoides intestinalis (PCI) is a rare condition.
  • Its clinical management and outcomes depend on manifestation severity.
  • True incidence may be higher than reported cases suggest.

Observation:

  • A 76-year-old woman with Crohn's disease presented with abdominal pain, distention, and weight loss.
  • Radiographs showed free intraperitoneal air; CT confirmed intestinal wall cysts, diagnosing PCI.
  • The patient lacked an acute abdomen, indicating nonoperative management was suitable.

Findings:

  • Nonoperative management with supportive care led to gradual symptom resolution.
  • The patient was discharged in stable condition and showed good follow-up results.
  • Free air in PCI cases does not automatically necessitate exploratory laparotomy.

Implications:

  • This case highlights that nonoperative management can be successful for select PCI patients.
  • It suggests a less invasive approach may be appropriate when acute surgical findings are absent.
  • Emphasizes the importance of individualized treatment based on clinical presentation in rare disorders like PCI.

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