Saudi Journal of Anaesthesia, 2022 Pheochromocytoma are catecholamine-producing neuroendocrine tumors that can be adrenal or extra-adrenal (paraganglioma) in origin. The mainstay of definitive therapy is surgical resection, and successful management depends on careful preoperative ...
Anil K Bhiwal +3 more
doaj +1 more source
Analysis of short-term blood pressure variability in pheochromocytoma/paraganglioma patients [PDF]
, 2019 Data on short-term blood pressure variability (BPV), which is a well-established cardiovascular prognostic tool, in pheochromocytoma and paraganglioma (PPGL) patients is still lack and conflicting.
Bisogni, V. +14 more
core +1 more source
Primary Retroperitoneal Inter-aorto-Caval Paraganglioma of the Organ of Zuckerkandl [PDF]
Journal of Clinical and Diagnostic Research, 2014 Tumour that arise from chromaffin cells at extra-adrenal locations are termed paragangliomas which are rare tumour. The organ of Zuckerkandl located along aortic bifurcation is the most common site of their occurrence.
Vaibhav Vikas +4 more
doaj +1 more source
Pheochromocytoma – clinical manifestations, diagnosis and current perioperative management [PDF]
, 2019 Pheochromocytoma is a neuroendocrine tumor characterized by the excessive production of catecholamines (epinephrine, norepinephrine, and dopamine). The diagnosis is suspected due to hypertensive paroxysms, associated with vegetative phenomena, due to the
Bratu, Ovidiu G +6 more
core +2 more sources
Non-functioning Aortocaval Paraganglioma Masquerading as Celiac Lymphnodal Metastasis
Eurasian Journal of Medicine, 2019 An extra-adrenal paraganglioma is a rare tumour derived from chromaffin cells of sympathetic ganglia. This report documents a rare case of a non-functional aortocaval paraganglioma in a 24-year-old woman with persistent abdominal pain.
Nikhil Gulavani +4 more
doaj +1 more source
Integrative multi-omics analysis identifies a prognostic miRNA signature and a targetable miR-21-3p/TSC2/ mTOR axis in metastatic pheochromocytoma/ paraganglioma [PDF]
, 2019 Artículo escrito por un elevado número de autores, solo se referencian el que aparece en primer lugar y los autores pertenecientes a la UAMPheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that present variable outcomes.
Alvarez - Escola, Cristina +1 more
core +2 more sources
Gangliocytic paraganglioma of the cauda equina: A rare tumor case report with literature review
Indian Spine Journal, 2023 Gangliocytic paragangliomas are rare, benign, encapsulated, and slow-growing tumors arising from the neuro-ectodermal ganglion or spindle cells. We describe the case of a 47-year-old male patient who presented to our department with intractable lower ...
Nigil Sadanandan Palliyil +3 more
doaj +1 more source
Extra-adrenal paraganglioma of prostate
Canadian Urological Association Journal, 2013 Extra-adrenal pheochromocytomas, or paragangliomas are rare tumors that may develop from extra-adrenal chromaffin cells, and most occur in the organ of Zuckerkandl. Extra-adrenal paraganglioma of the prostate is extremely rare. Here, we report a 53-year-old man with hypertension and lower urinary tract symptoms, who was initially diagnosed as benign ...
Hong-Hau, Wang +6 more
openaire +3 more sources
CT Imaging Findings of Extra-adrenal Abdominal Paragangliomas: A Case Series [PDF]
Journal of Clinical and Diagnostic ResearchExtra-adrenal paragangliomas are rare neuroendocrine tumours originating from paraganglia outside the adrenal glands. The present case series illustrates the Computed Tomography (CT) imaging features of three instances of extra-adrenal abdominal ...
Ssm Zainul Abidin Sarmast
doaj +1 more source
Risk Stratification on Pheochromocytoma and Paraganglioma from Laboratory and Clinical Medicine [PDF]
, 2018 Pheochromocytoma (PCC) and sympathetic paraganglioma (PGL) are rare neuroendocrine tumors characterized by catecholamine production in the adrenal medulla and extra-adrenal paraganglia.
Kimura Noriko +3 more
core +2 more sources