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

Adult and paediatric patients with pathogenic variants in the gene encoding succinate
dehydrogenase (SDH) subunit B (SDHB) often have locally aggressive, recurrent or …

Microwave thermal ablation offers a promising, minimally invasive therapeutic modality for
the management of functioning adrenocortical adenomas and adrenal metastases …

Image-guided radiofrequency ablation (RFA) has been accepted as a minimally invasive
treatment for adrenal tumors in patients who are unable to undergo adrenalectomy …

Methods A working group established by ESES reviewed the current guidelines and
undertook a literature search of the PubMed database focused on several clinical questions …

Background: Both selective and nonselective α-blockade are used for preoperative
preparation in patients with pheochromocytomas and paragangliomas (PPGLs). However …

INTRODUCTION—Pheochromocytoma is a rare neuroendocrine tumor, occurring in less
than 0.2 percent of patients with hypertension [1, 2]. In at least 25 percent of patients, the …

Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine neoplasms.
Approximately 85% of PPGLs are localized to the adrenal glands; the remaining 15% are …

Introduction Pheochromocytomas are rare neuroendocrine tumors that form in chromaffin
cells of the neural crest during the embryological period. In the overall population, incidence …

Pheochromocytomas and paragangliomas are catecholamines' producing tumors with
metastatic potential. In expert centers, new techniques have been developed, especially for …