Context: Because surgical and medical therapies of acromegaly all have specific limitations,
radiotherapy has been used as an adjunctive strategy. Stereotactic radiosurgery has not yet …

Pheochromocytomas/paragangliomas are characterized by a unique molecular landscape
that allows their assignment to clusters based on underlying genetic alterations. With around …

Purpose: Patients with succinate dehydrogenase subunit B(SDHB) mutation–related
pheochromocytoma/paraganglioma (PHEO/PGL) are at a higher risk for metastatic disease than …

The phenotypic heterogeneity of low-grade gliomas (LGGs) is still inconsistently explained
by known molecular abnormalities in patients treated according to the present standards of …

Pheochromocytomas/paragangliomas overexpress somatostatin receptors, and recent
studies have already shown excellent results in the localization of sympathetic succinate …

PET/CT comparing 68Ga-DOTATATE and other radiopharmaceuticals and in comparison with
CT/MRI for the localization of sporadic metastatic pheochromocytoma and paraganglioma …

Despite remarkable progress in imaging modalities and surgical management, persistence
or recurrence of primary hyperparathyroidism (PHPT) still occurs in 2.5–5% of cases of PHPT…

Multiple endocrine neoplasia type 2 (MEN2) is a rare hereditary syndrome due to mutations
of the proto-oncogene REarranged during Transfection (RET), defined by the association of …

In recent years, preoperative imaging has become essential in the evaluation of sporadic
primary hyperparathyroidism (HPT) for selecting good candidates for minimally invasive HPT. …

Neuroendocrine tumors overexpress somatostatin receptors, which serve as important and
unique therapeutic targets for well-differentiated advanced disease. This overexpression is a …