Chronic Sarcoidosis with Mycetomas and Cardiac Involvement
Imaging findings
A middle-aged patient with upper-lobe-predominant nodular and fibrotic sarcoidosis (perilymphatic nodules, apical fibrosis) on a 2008 CT progressed by 2015 to fibrocavitary upper lobe disease with a mycetoma, later requiring right upper lobectomy. A 2020 CT shows left upper lobe mycetomas with a surrounding rind of tissue and a positive serum galactomannan, in a steroid-treated, immunocompromised patient. Cardiac MRI shows T2 hyperintensity in the septum and LV apex with septal and RV late gadolinium enhancement, consistent with cardiac sarcoidosis.
Key takeaways
End-stage fibrocavitary sarcoidosis is a substrate for aspergillus colonization producing mycetomas, and a positive galactomannan with a wall of tissue around the cavity may reflect subacute (semi-invasive) aspergillosis, though the cavity-wall thickening can also represent an ABPA-like allergic response to intracavitary aspergillus. The same patient demonstrates cardiac sarcoidosis with the classic mid-myocardial/septal late gadolinium enhancement pattern.
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