Abdominal Cocoon Syndrome Secondary to Signet Ring Cell Adenocarcinoma: A Rare Diagnostic Challenge
Umbish Dino1, Ahamed Lazim Vattoth2, Jeremy Smith1
1Department of Internal Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Introduction:
Abdominal cocoon syndrome, or sclerosing encapsulating peritonitis, is a rare condition characterized by the encasement of the small bowel in a dense fibrocollagenous membrane, often mimicking symptoms of bowel obstruction. Secondary ACS associated with malignancy is exceptionally uncommon.
Case Presentation:
A 44-year-old man with a history of ascites presented with intractable nausea, vomiting and severe cachexia. The diagnostic process posed significant challenges, requiring advanced imaging and invasive interventions to uncover the underlying malignancy.
Discussion:
This case highlights the diagnostic challenges of secondary abdominal cocoon syndrome, emphasizing the importance of maintaining high clinical suspicion and utilizing advanced diagnostic tools in complex presentations.
Conclusions:
Early recognition, advanced imaging, and a multidisciplinary approach are critical to optimizing outcomes in rare and challenging conditions.
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