Spontaneous esophageal perforation in a patient with mixed connective tissue disease

David Lyman1

  • 1Cherry Street Health Services, 100 Cherry Street SE, Grand Rapids, Michigan, 49053, USA.

Insights

Spontaneous esophageal perforation is a rare but serious condition. Delayed diagnosis in this case led to severe complications, highlighting the need for timely recognition of esophageal perforation, especially in patients with connective tissue disease.

Area of Science:

  • Medicine
  • Gastroenterology
  • Rheumatology

Background:

  • Spontaneous esophageal perforation is a rare, life-threatening condition with a poor prognosis if not diagnosed within 24-48 hours.
  • Patients with mixed connective tissue disease (MCTD) on immunosuppressants may present with atypical symptoms.

Purpose of the Study:

  • To highlight a case of delayed diagnosis of spontaneous esophageal perforation in a patient with MCTD.
  • To emphasize the importance of timely diagnosis and management of esophageal perforation to improve patient outcomes.

Main Methods:

  • Case report of a patient with MCTD presenting with symptoms initially attributed to community-acquired pneumonia (CAP).
  • Review of literature concerning spontaneous esophageal perforation diagnosis and management.

Main Results:

  • The patient presented with chest/shoulder pain, hydropneumothorax, respiratory failure, and shock, initially treated for CAP and bilateral yeast empyemas.
  • Diagnosis of esophageal perforation was only considered on day 26 after the development of mediastinitis.
  • Literature review indicated potential for more timely diagnosis and management.

Conclusions:

  • Delayed diagnosis of spontaneous esophageal perforation can lead to catastrophic outcomes.
  • Early consideration of esophageal perforation is crucial, particularly in immunocompromised patients or those with connective tissue diseases presenting with severe symptoms.
  • Timely intervention can significantly improve prognosis in cases of esophageal perforation.

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