Exploring Head and Neck Paraganglioma: A Case Report
- PMID: 38586626
- PMCID: PMC10998543
- DOI: 10.7759/cureus.55720
Exploring Head and Neck Paraganglioma: A Case Report
Abstract
Paragangliomas (PGLs) are tumors that are rarely malignant; the majority of them are benign. Similar to pheochromocytoma, they develop from the autonomic nerve system. This system originates from neural crest cells and can undergo neoplastic transformation. PGLs can arise either inside or outside the adrenal glands. Head and neck PGLs are very scarce. The primary locations where this tumor commonly originates within this region are the carotid body, jugular bulb, and vagal body. Hence, in our case report, we attempt to highlight the uncommon presentation of this disease in a 46-year-old female, who initially presented with hypertension and persistent dysphonia. The patient underwent successful external radiotherapy. This case report aims to raise awareness of the characteristics of these rare malignancies.
Keywords: autonomic nerve system; cancer; head and neck; paraganglioma; pheochromocytoma.
Copyright © 2024, Samba et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
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