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Virus and Autoimmunity: Can SARS-CoV-2 Trigger Large Vessel Vasculitis?
João Lázaro Mendes1, Gabriela Venade1, Paula Manuel1
1Internal Medicine Department, Centro Hospitalar Tondela-Viseu, Viseu, Portugal.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can trigger large vessel vasculitis (LVV) in susceptible individuals. Prompt diagnosis and treatment of autoimmune diseases post-COVID-19 improve patient prognosis.
Area of Science:
- Rheumatology
- Infectious Diseases
- Immunology
Background:
- Viral infections, including SARS-CoV-2, are increasingly linked to autoimmune diseases.
- Rheumatic conditions like vasculitis and arthritis have been observed following COVID-19.
- Large vessel vasculitis (LVV) is a less commonly reported post-viral autoimmune manifestation.
Purpose of the Study:
- To report a case of large vessel vasculitis (LVV) temporally associated with SARS-CoV-2 infection.
- To highlight the potential for SARS-CoV-2 to trigger autoimmune responses beyond typical rheumatic manifestations.
- To emphasize the importance of considering LVV in patients with post-viral inflammatory syndromes.
Main Methods:
- Case report of a 19-year-old woman with symptoms 5 weeks after mild COVID-19.
- Diagnostic work-up included serological tests, computed tomography (CT), and fluorodeoxyglucose positron emission tomography (FDG-PET).
- Treatment involved prednisolone, with subsequent normalization of symptoms and laboratory values.
Main Results:
- The patient presented with fatigue, malaise, chest, and low back pain, indicative of a proinflammatory state.
- Imaging revealed inflammatory changes in the aorta and proximal iliac and renal arteries, consistent with LVV.
- Prednisolone treatment led to symptom resolution and normalization of inflammatory markers.
Conclusions:
- Recent SARS-CoV-2 infection can precipitate large vessel vasculitis, such as Takayasu arteritis.
- Early recognition and differential diagnosis of LVV are crucial to exclude mimics.
- Physicians must be aware of the broad spectrum of autoimmune diseases potentially triggered by SARS-CoV-2 for timely intervention and improved outcomes.
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