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Granulomatosis with polyangiitis: Common and uncommon presentations.
Qiao Xin Tee1, Aaron Wong1, Mithun Nambiar1,2
1Monash Imaging, Monash Health, Clayton, Victoria, Australia.
Granulomatosis with polyangiitis (GPA) is an autoimmune small vessel vasculitis. This review highlights key imaging findings suggestive of GPA in various organ systems, aiding diagnosis and monitoring.
Area of Science:
- Radiology
- Immunology
- Rheumatology
Background:
- Granulomatosis with polyangiitis (GPA) is a rare autoimmune disease affecting small blood vessels.
- It primarily impacts the respiratory and renal systems but can involve other organs.
- Early diagnosis and monitoring are crucial for managing GPA.
Observation:
- No single imaging finding is definitive for GPA.
- Characteristic radiological patterns exist across different organ systems.
- Imaging is vital when correlated with clinical and laboratory data.
Findings:
- This pictorial review details common and rare imaging manifestations of GPA.
- Radiological features in the respiratory, renal, CNS, orbital, cardiac, and GI systems are presented.
- Understanding these patterns aids in differentiating GPA from other vasculitides.
Implications:
- Accurate radiological assessment supports timely GPA diagnosis.
- Imaging helps monitor treatment response and disease progression.
- This review serves as a visual guide for clinicians managing GPA.
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