Discussion
Diagnosis With Brief Discussion
- Diagnosis
- EGPA (eosinophilic granulomatosis with polyangiitis, Churg-strauss syndrome)
- Radiologic Findings
- Fig.1. Chest PA.
Bilateral patchy consolidations.
Fig 2. Chest CT.
Patchy consolidations and GGOs in bilateral lungs.
Mild bronchial wall thickening in the right lower lobe.
Small to borderline-sized reactive LNs in bilateral mediastina and hilar.
Small amount of pleural effusion.
Fig 3. Paranasal sinus series.
Air-fluid level in Rt. Maxillary sinus, R/O acute sinusitis.
Peripheral eosinophilia was found on laboratory test.
- Brief Review
- Formerly known as Churg-Strauss syndrome, it is characterized by asthma, eosinophilia, and necrotizing vasculitis. Asthma is present in almost all patients and peripheral neuritis is seen in about 75% of patients. Symptoms and signs vary over time, with the first 8 to 10 years of life characterized by atopy, sinusitis, and asthma, followed by an increase in eosinophils in the peripheral blood and gradual deposition of eosinophils in the lungs and other organs, followed by vasculitis and systemic symptoms such as fever and weight loss.
The lungs are the most commonly involved organ, and pulmonary hemorrhage or glomerulonephritis are much rarer when compared to GPA and MPA. The heart can be involved, with coronary arteritis and myocarditis being the main causes of death. Approximately 40-75% of patients with EGPA have ANCA, most often p-ANCA.
The most common plain radiography imaging findings of EGPA are transient, patchy, non-segmental, bilateral pulmonary involvement with no specific areas of consolidation. On CT, small nodules, ground-glass opacities, bronchial thickening or dilation, pulmonary consolidation, interlobular septal thickening, and mosaic perfusion are common findings.
- References
- J Korean Soc Radiol 2021;82(4):791-807
AJR 1998;1 70:297-300
Respiratory Medicine Case Reports 21 (2017) 1-6
- Keywords
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