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Autoimmune Ascites Responding to Mycophenolate Mofetil: A Case Report
Douglas A Simonetto1, Hala Fatima2, Folkert Zijlstra3
1Department of Gastroenterology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
This case study introduces autoimmune ascites, a rare condition. Treatment with mycophenolate mofetil resolved symptoms, suggesting its efficacy for this previously unreported cause of ascites.
Area of Science:
- Gastroenterology and Immunology
- Internal Medicine
- Clinical Case Reports
Background:
- Ascites, characterized by peritoneal fluid accumulation, commonly stems from portal hypertension due to cirrhosis.
- Malignancy, heart failure, tuberculosis, and pancreatic disease are other recognized causes of ascites.
- Autoimmune ascites has not been previously documented in medical literature.
Observation:
- A 67-year-old male presented with refractory ascites, including abdominal distention and weight gain.
- A three-year diagnostic workup revealed a serum-ascites albumin gradient > 1.1 g/dL and ascitic fluid protein of 3.0 g/dL.
- Peritoneal biopsies showed minimal inflammatory changes, and common/rare causes of ascites were excluded.
Findings:
- The patient's ascites was refractory to standard treatments.
- Empiric treatment with mycophenolate mofetil (CellCept) led to symptom resolution.
- Symptom resolution persisted for over two years without the need for repeat paracentesis.
Implications:
- This case suggests autoimmune ascites as a potential, previously unreported etiology.
- Mycophenolate mofetil may be an effective treatment for autoimmune ascites.
- Further research is warranted to confirm autoimmune ascites and its therapeutic strategies.
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