S3844 Incidental, Idiopathic Pneumoperitoneum in an Asymptomatic Patient

Introduction: IP remains an enigmatic condition in clinical practice, with no clear consensus on its etiology. While often incidental, the diagnosis requires careful differentiation from more common causes of free air in the abdomen, emphasizing the importance of thorough evaluation and management. Case Description/Methods: A 76-year-old woman with prior history of DM II, hyperlipidemia, medullary thyroid cancer post-thyroidectomy, CHF presented to the ER after her Holter monitor revealed intermittent third degree AVB. She was asymptomatic with no complaints. On presentation, she was stable, with normal vitals except for occasional dips in HR to the 40s. A CXR revealed pneumomediastinum, prompting further imaging. A CT scan showed not only pneumomediastinum but also pneumoperitoneum in the upper abdomen, raising concern for a possible perforated viscus. She was admitted to the ICU for monitoring with placement of a temporary TVP pending PPM placement. Despite the concerning imaging, her clinical exam showed a soft, non-tender abdomen with no signs of acute distress, and her lab work remained stable. General Surgery performed a diagnostic ex-lap, which revealed no perforation, though the presence of sevoflurane in the abdomen suggested an abnormal communication between the thorax and abdomen, potentially from a ruptured mediastinal bleb. The ex-lap ruled out a perforated viscus or colon. A PPM was successfully placed, and the patient was discharged in stable condition on oral AC, with plans for close follow-up and monitoring. Discussion: Idiopathic pneumoperitoneum (IP) is a rare subtype of pneumoperitoneum, and a diagnosis of exclusion. It typically requires conservative management and serial monitoring. It is most often caused by GI perforation, with other manifestations like pneumatosis intestinalis and portal venous gas linked to acute GI ischemia, both associated w/high mortality rates. Theories on the pathogenesis of IP include mechanical pressure, bacterial gas production, and intra-mural gas blebs, the latter of which was considered in this case as a potential cause for free air in the peritoneum. IP can be found incidentally in asymptomatic patients, often during routine screenings such as CXRs or CT scans. These patients may not exhibit typical signs of peritonitis, making diagnosis particularly challenging. Management of IP is typically conservative, with careful observation. Although recurrence is rare, there have been instances of IP reappearing years later, necessitating long-term monitoring.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001142836.10039.40
Primary Topic
Appendicitis Diagnosis and Management
Type
article
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article

S3844 Incidental, Idiopathic Pneumoperitoneum in an Asymptomatic Patient

Stephen Klepner, Emad Zarief Kamel, Riddhi Machchhar, Eric Ball et al.
The American Journal of Gastroenterology
Appendicitis Diagnosis and Management
article

S3844 Incidental, Idiopathic Pneumoperitoneum in an Asymptomatic Patient

Stephen Klepner, Emad Zarief Kamel, Riddhi Machchhar, Eric Ball, Matthew H. Friedland
article en

Abstract

Introduction: IP remains an enigmatic condition in clinical practice, with no clear consensus on its etiology. While often incidental, the diagnosis requires careful differentiation from more common causes of free air in the abdomen, emphasizing the importance of thorough evaluation and management. Case Description/Methods: A 76-year-old woman with prior history of DM II, hyperlipidemia, medullary thyroid cancer post-thyroidectomy, CHF presented to the ER after her Holter monitor revealed intermittent third degree AVB. She was asymptomatic with no complaints. On presentation, she was stable, with normal vitals except for occasional dips in HR to the 40s. A CXR revealed pneumomediastinum, prompting further imaging. A CT scan showed not only pneumomediastinum but also pneumoperitoneum in the upper abdomen, raising concern for a possible perforated viscus. She was admitted to the ICU for monitoring with placement of a temporary TVP pending PPM placement. Despite the concerning imaging, her clinical exam showed a soft, non-tender abdomen with no signs of acute distress, and her lab work remained stable. General Surgery performed a diagnostic ex-lap, which revealed no perforation, though the presence of sevoflurane in the abdomen suggested an abnormal communication between the thorax and abdomen, potentially from a ruptured mediastinal bleb. The ex-lap ruled out a perforated viscus or colon. A PPM was successfully placed, and the patient was discharged in stable condition on oral AC, with plans for close follow-up and monitoring. Discussion: Idiopathic pneumoperitoneum (IP) is a rare subtype of pneumoperitoneum, and a diagnosis of exclusion. It typically requires conservative management and serial monitoring. It is most often caused by GI perforation, with other manifestations like pneumatosis intestinalis and portal venous gas linked to acute GI ischemia, both associated w/high mortality rates. Theories on the pathogenesis of IP include mechanical pressure, bacterial gas production, and intra-mural gas blebs, the latter of which was considered in this case as a potential cause for free air in the peritoneum. IP can be found incidentally in asymptomatic patients, often during routine screenings such as CXRs or CT scans. These patients may not exhibit typical signs of peritonitis, making diagnosis particularly challenging. Management of IP is typically conservative, with careful observation. Although recurrence is rare, there have been instances of IP reappearing years later, necessitating long-term monitoring.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 55%
Appendicitis Diagnosis and Management
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