Phaeochromocytoma and paraganglioma (PPGL) are chromaffin cell tumours that require
timely diagnosis because of their potentially serious cardiovascular and sometimes life …

Simple Summary Pheochromocytomas and abdominal paragangliomas (PPGLs) are rare.
They can be discovered incidentally by imaging with computed tomography or magnetic …

This manuscript is the result of the North American Neuroendocrine Tumor Society
consensus conference on the medical management and surveillance of metastatic and …

This first part of a two-part review of pheochromocytoma and paragangliomas (PPGLs)
addresses clinical presentation, diagnosis, management, treatment, and outcomes. In this …

Pheochromocytomas (PCCs) are rare neuroendocrine tumors. About 80% to 85% of these
cancers arise from chromaffin cells residing in the adrenal medulla. The remaining 15% to …

Simple Summary Non-invasive characterization of adrenal lesions requires a rigorous
approach. Although CT is the cornerstone of adrenal lesion characterization, a multimodality …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors arising
from chromaffin cells of the adrenal medulla or extra-adrenal paraganglia, respectively …

Abstract Purpose of Review To discuss selected endocrine causes of hypertension and to
provide practical clinical recommendations regarding the evaluation and treatment of these …

As a rare kind of non-epithelial neuroendocrine neoplasms, paragangliomas (PGLs) exhibit
various clinical characteristics with excessive catecholamine secretion and have been a …

Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors, a large
proportion of which secrete catecholamines. PPGL are associated with a high …