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Published on: June 28, 2021
Silence pancreatitis in systemic lupus erythematosus
Ervin Alibegovic1, Admir Kurtcehajic2, Ismar Hasukic1
1Department of Gastroenterology and Hepatology, University Clinical Center Tuzla, Tuzla, Bosnia and Herzegovina.
Systemic lupus erythematosus (SLE) can lead to silent pancreatitis, a condition that may be missed despite its severe consequences. Early detection of this complication is crucial for patient outcomes in SLE management.
Area of Science:
- Rheumatology
- Gastroenterology
- Radiology
Background:
- Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with diverse clinical manifestations.
- Pancreatitis is a known, though less common, complication of SLE and its treatments.
Observation:
- A 35-year-old female SLE patient with high disease activity (SLE Disease Activity Index > 15) presented with disease exacerbation.
- Computed tomography (CT) was used to assess pancreatitis in this patient.
- The pancreatitis was subclinical and biochemically silent, meaning it presented without typical symptoms or lab abnormalities.
Findings:
- Despite increased immunosuppressive therapy (corticosteroids and azathioprine), a biochemically silent pancreatitis developed.
- The silent pancreatitis was not diagnosed in a timely manner.
- The patient ultimately died from multisystem organ failure attributed to the undiagnosed pancreatitis.
Implications:
- This case highlights the potential for clinically and biochemically silent pancreatitis as a severe complication in SLE patients.
- It underscores the importance of considering pancreatitis in SLE patients, even in the absence of typical symptoms or biochemical markers.
- Radiological assessment, such as CT, may be vital for diagnosing silent pancreatitis in this population.
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