Pheochromocytoma and Paraganglioma
Pheochromocytoma and paraganglioma are rare, possibly malignant, catecholamine secreting tumors. These tumors arise from the adrenal medulla and extra-adrenal sites, with reports of 80-85% and 15-20% respectively.
Foltz, Christopher
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Management of para-aortic paraganglioma in a patient with uncontrolled blood pressure-a case report. [PDF]
Alshehri K +3 more
europepmc +1 more source
From chromaffin cells to Phaeochromocytoma: insight into the sympathoadrenal cell lineage
Chromaffin cells are a modified post-ganglionic sympathetic neuron, which synthesise and secrete catecholamines. The neoplastic transformation of chromaffin cells is demonstrated by the tumour phaeochromocytoma, a functional tumour that recapitulates the
Cleary, Susannah
core
Malignant Extra-adrenal Paraganglioma of the Bladder: A Rare Clinical Entity. [PDF]
Korrapati VR +4 more
europepmc +1 more source
Paragangliomas are non-epithelial tumours originating from neural crest-derived paraganglion cells situated in the region of the autonomic nervous system ganglia and accompanying nerves.
Capella, C. +16 more
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Preoperative Adrenal Artery Embolization in a Pediatric Patient with Bilateral Pheochromocytomas: A Case Report. [PDF]
Moya Ochoa C +4 more
europepmc +1 more source
A Case of Functional Para-Aortic Paraganglioma Causing Accelerated Hypertension in an HIV-Positive Patient With Negative 68Ga-DOTATATE PET/CT Findings: Successful Laparoscopic Management. [PDF]
Rajaian S +4 more
europepmc +1 more source
From Tissue Architecture To Genetic Signature: Artificial intelligence-based Analysis of Reticulin Framework and Clinical Variables Predicts Molecular Cluster in Paragangliomas. [PDF]
Duregon E +13 more
europepmc +1 more source

