Von Hippel-Lindau Pheochromocytomas, CT
Computed tomography (CT) scan with contrast media of bilateral pheochromocytomas (arrows). This patient has von Hippel-Lindau syndrome. A pheochromocytoma or phaeochromocytoma (PCC) is a neuroendocrine tumor of the medulla of the adrenal glands (originating in the chromaffin cells), or extra-adrenal chromaffin tissue that failed to involute after birth and secretes high amounts of catecholamines, mostly epinephrine, plus norepinephrine to a lesser extent. Von Hippel-Lindau disease (VHL) is a disease which results from a mutation in the von Hippel-Lindau tumor suppressor gene on chromosome
Size: 3750px × 3750px
Photo credit: © Photo Researchers / Alamy / Afripics
License: Licensed
Model Released: No
Keywords: -invasive, abnormal, adrenal, bilateral, cancer, cancerous, carcinoma, cell, ct, cytopathological, cytopathology, diagnostic, disease, diseased, growth, hippel-lindau, histopathological, histopathology, image, imaging, institute, magnetic, malignancy, malignant, medical, medicine, mri, mrt, national, nci, neoplasm, nmr, nmri, nuclear, pathological, pathology, pcc, phaeochromocytoma, pheochromocytoma, pheochromocytomas, radiology, resonance, science, syndrome, technique, test, tomography, tumor, tumour, unhealthy, vhl, von
