• The specific situation of the patient. Unless otherwise provided for by national regulations,
off-label use of medication should be limited to situations where it is in the patient's interest …

Pheochromocytomas and paragangliomas are rare neuroendocrine tumours. Around 20-
25% of patients develop metastases, for which there is an urgent need of prognostic markers …

Pheochromocytomas and sympathetic paragangliomas (PPGL) are rare neuroendocrine
tumors originating from chromaffin tissue of the adrenal medulla and extra-adrenal …

Malate dehydrogenase (MDH) is pivotal in mammalian tissue metabolism, participating in
various pathways beyond its classical roles and highlighting its adaptability to cellular …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors
originating from chromaffin cells, holding significant clinical importance due to their capacity …

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors derived
from neural crest cells from adrenal medullary chromaffin tissues or extra-adrenal …

The parasellar region is the anatomical area around the sella turcica that represents a
crucial crossroad for important adjacent structures. Several distinct tumors can primarily …

Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors derived
from chromaffin cells in the autonomic nervous system. Depending on their location, these …

This retrospective study explores the utility of near-infrared (NIR) fluorescence imaging with
indocyanine green (ICG) in enhancing the intraoperative identification and guidance for the …

Adrenocortical carcinoma (ACC) and pheochromocytoma/paraganglioma (PPGL) are two
rare types of adrenal gland malignancies. Regarding hereditary tumors, some patients with …