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Post-COVID-19 polyautoimmunity - Fact or coincidence: A case report
Ali Ibrahim Shorbagi1, Abdulmunhem Obaideen2, Majd Jundi3
1Clinical Sciences Department, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
COVID-19 can trigger autoimmune conditions like colitis and pancreatitis. This case highlights the need for vigilance in patients with a history of COVID-19, as conventional treatments show good response rates.
Area of Science:
- Gastroenterology
- Immunology
- Infectious Diseases
Background:
- COVID-19 shares clinical and immunological similarities with systemic autoimmune diseases.
- Rare instances of COVID-19 triggering ulcerative colitis and autoimmune hepatitis have been reported.
Observation:
- A previously healthy, vaccinated male presented with symptoms of chronic colitis, autoimmune pancreatitis, and AIH-like hepatitis two months post-COVID-19 infection.
- Clinical presentation included abdominal pain, nausea, vomiting, and persistent bloody diarrhea.
- Diagnostic workup revealed acute pancreatitis, chronic colitis resembling ulcerative colitis, and findings suggestive of autoimmune pancreatitis and immune-mediated hepatitis.
Findings:
- Treatment with intravenous prednisolone led to rapid improvement in bloody diarrhea within 72 hours.
- Elevated liver enzymes normalized following steroid therapy, with positive autoimmune markers (ANA, anti-smooth muscle antibodies).
- The patient achieved symptom remission on mesalazine and azathioprine, remaining symptom-free seven months post-diagnosis.
Implications:
- A high index of suspicion for autoimmune disorders is warranted in patients with a history of COVID-19.
- Conventional treatments for autoimmune conditions demonstrate efficacy in post-COVID-19 cases.
- Early diagnosis and management can lead to good response and remission rates.
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