Abstract Library
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#4567 Malignant pheochromocytoma with late distant metastases and secondary hypercalcaemia
Introduction: Pheochromocytoma is a rare neuroendocrine tumour of the adrenal medulla. Malignant variants occur with a very low frequency and can be diagnosed only after the spread of distant metastasis.
Conference:
Presenting Author:
Authors: Kirova I, Vandeva S, Markova M, Elenkova A, Robeva R,
Keywords: neuroendocrine, malignant pheochromocytoma, metastasis, hypercalcaemia,
Introduction: Paragangliomas (PPGLs) are rare neuroendocrine tumors that may secrete catecholamines and their metabolites (metanephrines [MN], normetanephrine [NMN]). Secretion patterns differ by adrenal/extra-adrenal origin and genetic alteration. Catecholamines synthesis is carried by phenylalanine hydroxylase (PAH), tyrosine hydroxylase (TH), aromaticL-aminoacid decarboxylase (AADC), dopamine β-hydroxylase (DBH) and phenylethanolamine N-methyltransferase (PNMT). However, their regulation in PPGL is not entirely understood.
Conference:
Presenting Author: Tirosh A
Authors: Kaplinsky A, Halperin R, Shlomai G, Tirosh A,
Keywords: ppgl, methylation, catecholamine, pseudohypokia, metanephrine, kinase signaling, pheochromocytoma, paraganglioima,
Introduction: SSR PET/CT is used in workup of pts with PCC/ PGL. Correlation of tumour burden on PET & biomarkers 24 hr Urine Metanephrines (UMET), normetanephrine (UNMET), UMET:creatinine ratio (MET:Crea),UNMET:creatinine (UNMET:crea) & Chromogranin A (CGA) has not been done.
Conference: 15th Annual ENETSConcerence (2018)
Presenting Author: Steyn R
Keywords: 68Ga DOTANOC PET CT, PGL, PCC,
Introduction: “Composite” pheochromocytoma is a rare tumor, consisting of pheochromocytoma and neuroblastic tumors. The definite diagnosis is histological. Subclinical Cushing's syndrome refers to autonomous glucocorticoid production without specific signs and symptoms of Cushing's syndrome.
Conference: 13th Annual ENETSConcerence (2016)
Presenting Author: Kiraly A
Authors: Kiraly A, Muntean V, Domsa I, Ghervan C,
Keywords: adrenal, composite, pheochromocytoma, ganglioneuroma, hypercorticism.,
Introduction: Paragangliomas have hereditary and sporadic presentations.
Conference: 11th Annual ENETSConcerence (2014)
Presenting Author:
Authors: Wandurraga E, Marín L,
Keywords: paraganglioma, pheochromocytoma, metanephrines, vanillylmandelic acid,