Why the study?
Paragangliomas are extremely rare neuroendocrine tumors that are barely found in the middle mediastinum.
Population
A 31-year-old male with an incidentally found middle mediastinal tumor
Design
Case report
Follow-up
4 year
Authors
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Incidental echocardiography detection of rare middle mediastinal paraganglioma extends sparse case literature; leaves open optimal diagnostic and management strategies.
Complete surgical excision of a middle mediastinal paraganglioma enclosing the LAD with concurrent CABG is feasible and can result in long-term recurrence-free survival.
Zhang et al. (2022) studied this question.
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