AI Article Synopsis

  • Acute pancreatitis (AP) is a rare but severe complication that can occur in patients with systemic lupus erythematosus (SLE), making diagnosis and treatment challenging.
  • A 20-year-old female with SLE experienced sudden severe abdominal pain, vomiting, and systemic inflammation, leading to lab tests confirming AP through elevated amylase and lipase levels.
  • The patient underwent aggressive treatment, including fluid resuscitation and intensive care monitoring, emphasizing the necessity for quick diagnosis and a coordinated care approach for SLE-related AP.

Article Abstract

Acute pancreatitis (AP) is a rare but life-threatening complication in patients with systemic lupus erythematosus (SLE). The case highlights the diagnostic challenges and treatment complexities in managing SLE-associated pancreatitis. A 20-year-old female with a history of SLE presented with acute onset epigastric pain, vomiting, and signs of systemic inflammation. Laboratory findings revealed elevated amylase and lipase levels, confirming AP. Imaging studies showed interstitial edematous pancreatitis and bilateral pleural effusion. The patient was managed with aggressive fluid resuscitation, pain management, and supportive care. A systemic inflammatory response complicated her clinical course, and she required intensive care unit monitoring. This case underscores the importance of early recognition of AP in SLE patients and highlights the need for a multidisciplinary approach to manage this severe complication.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11584975PMC
http://dx.doi.org/10.1002/ccr3.9621DOI Listing

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