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[Aortitis: report of three cases].
Summary
Aortitis, inflammation of the aorta, presents with varied symptoms and is often diagnosed via imaging. This study details three distinct cases, highlighting diverse causes and successful treatment strategies for this rare condition.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Immunology
Background:
- Aortitis, inflammation of the aortic wall, encompasses diverse etiologies including inflammatory, infectious, paraneoplastic, and idiopathic diseases.
- Diagnosis often necessitates a high clinical suspicion due to variable and nonspecific symptoms, frequently being an incidental finding.
- Imaging studies are crucial for confirming the diagnosis of aortitis.
Observation:
- Case 1: A 29-year-old woman with alopecia, oral/nasal ulcers, and positive antinuclear antibodies presented with thoracic aorta thickening, dilation, and stenosis.
- Case 2: A 41-year-old male with dorsal pain and cough showed descending aorta thickening and celiac artery stenosis, diagnosed as polyangiitis.
- Case 3: A 28-year-old woman with upper abdominal pain exhibited aortic arch and subclavian artery thickening, diagnosed as sarcoidosis.
Findings:
- Successful treatment in Case 1 involved steroids, hydroxychloroquine, cyclophosphamide, and azathioprine.
- Cases 2 and 3 were managed with corticosteroids and immunosuppressants (cyclophosphamide, azathioprine) tailored to their specific diagnoses.
- These cases illustrate the varied clinical presentations and successful management of different forms of aortitis.
Implications:
- Highlights the importance of considering aortitis in patients with unexplained systemic symptoms and vascular abnormalities.
- Demonstrates the efficacy of multimodal immunosuppressive therapy in managing diverse aortitis presentations.
- Emphasizes the role of advanced imaging in diagnosing and characterizing aortic inflammation and its complications.
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