| Literature DB >> 35438784 |
Nwadinma U Emeruem1, Christopher C Muoghalu2, Ndubueze Ezemba1.
Abstract
Carotid body tumors, rare neck paragangliomas arising from the common carotid artery bifurcation, can be classified as sporadic, hyperplastic, or familial. The familial type is often bilateral and associated with germline mutation of the mitochondrial enzyme succinate dehydrogenase. We report the rare case of a 42-year-old man who presented with bilateral giant familial carotid body tumors associated with a concomitant skull-base paraganglioma, left-sided facial nerve palsy, and an incomplete circle of Willis. We describe the excision of the tumors in 2 stages (the left mass and associated paraganglioma first and the right mass second), 6 months apart, with use of general anesthesia, and we discuss other operative considerations.Entities:
Keywords: Carotid body tumor/classification/diagnosis/pathology/surgery; cranial nerve diseases; facial nerve diseases; head and neck neoplasms/pathology/surgery; paraganglioma/diagnosis/therapy; treatment outcome
Mesh:
Year: 2022 PMID: 35438784 PMCID: PMC9053652 DOI: 10.14503/THIJ-20-7370
Source DB: PubMed Journal: Tex Heart Inst J ISSN: 0730-2347