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CASE REPORT
Catecholamine-secreting paraganglioma: the challenges of perioperative management
  1. Eamon Shamil1,
  2. Liam Brennan2,
  3. Piyush Jani1
  1. 1ENT Surgery Department, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK
  2. 2Anaesthetic Department, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK
  1. Correspondence to Eamon Shamil, eamonshamil{at}gmail.com

Summary

An asymptomatic 48-year-old man presented with a right-sided neck mass. A CT scan demonstrated a lesion at the carotid bifurcation and an angiogram showed splaying of the carotid arteries. His plasma metanephrines were raised confirming a catecholamine-secreting paraganglioma. Metaiodobenzylguanidine single-photon emission CT showed focal high tracer uptake in the right of the neck. Histology revealed a tumour, arising within a nerve, composed of oval-shaped cells arranged in nested (zellballen) as well as in trabecular patterns. Immunohistochemistry was positive for neuroendocrine markers chromogranin A, synaptophysin and CD56. Preoperative management included an endocrinologist initiating α-adrenergic and β-adrenergic blockers. Intraoperatively, acute hypertension occurred whenever the tumour was manipulated. Close communication between the surgeons and the anaesthetist allowed for these episodes to be predicted and treated with fast-acting antihypertensives such as sodium nitroprusside. Postoperatively, the patient recovered well and his antihypertensives were discontinued.

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