DOI: https://doi.org/10.36347/sjmcr.2024.v12i10.040

Pages: 1774-1777

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 [1]. The primary locations where this tumor commonly originates within this region are the carotid body, jugular bulb, and vagal body. In our case report, a 65-year-old man, who presented with a firm, painless, pulsatile neck mass that increased in size over the course of months. The diagnosis was suspected based on the patient’s clinical history and physical examination. The diagnosis was confirmed with CT angiography (CTA).