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Published in 2022 at "BMJ Case Reports"
DOI: 10.1136/bcr-2021-247023
Abstract: Pheochromocytoma and paraganglioma (PGL) are rare neuroendocrine tumours, frequently associated with genetic syndromes. We report the case of a man in his 40s with a left anterior neck mass and a history of hypertensive crisis,…
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Keywords:
pgl4 syndrome;
syndrome patient;
paraganglioma;
pheochromocytoma ... See more keywords