Results 11 to 20 of about 73,068 (324)
BMJ Case Reports, 2020 A man in his 70s, with a history of a glomus jugulare paraganglioma diagnosed 18 years ago, presented with an unprovoked deep vein thrombosis (DVT). The paraganglioma had been treated by radiotherapy, and yearly scans had not shown any progression since ...
Daniela Harmsworth +3 more
semanticscholar +3 more sources
Risk Stratification on Pheochromocytoma and Paraganglioma from Laboratory and Clinical Medicine [PDF]
Journal of Clinical Medicine, 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 +3 more sources
Personalized Management of Pheochromocytoma and Paraganglioma
Endocrine reviews, 2021 Pheochromocytomas/paragangliomas are characterized by a unique molecular landscape that allows their assignment to clusters based on underlying genetic alterations.
S. Nölting +8 more
semanticscholar +1 more source
Journal of the College of Physicians and Surgeons Pakistan, 2021 Sir, Paragangliomas are rare tumors originating from paraganglionic tissue that extends from the skull base to the pelvic diaphragm. Although they can be asymptomatic, they can also cause symptoms by secreting catecholamines or with local expansion. They can also be the component of many hereditary diseases.
Yılmaz, Fahri +2 more
openaire +4 more sources
Genomic and immune landscape Of metastatic pheochromocytoma and paraganglioma
Nature Communications, 2023 The molecular mechanisms underlying metastasis in pheochromocytoma/paraganglioma (mPPGL) remain to be explored. Here, the authors perform genomic and immunogenomic profiling of mPPGL tumors and suggest potential biomarkers for risk of metastasis and ...
Bruna Calsina +52 more
semanticscholar +1 more source
Pheochromocytoma/paraganglioma-associated cardiomyopathy
Frontiers in Endocrinology, 2023 Pheochromocytoma/paraganglioma (PPGL) are neuroendocrine tumors that frequently produce and release catecholamines. Catecholamine excess can manifest in several cardiovascular syndromes, including cardiomyopathy. PPGL-induced cardiomyopathies occur in up
Alicja Szatko +2 more
semanticscholar +1 more source
New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical Implications
Cancers, 2022 Simple Summary Pheochromocytoma and paraganglioma (together PPGL) are rare neuroendocrine tumors that arise from chromaffin tissue and produce catecholamines.
S. Jhawar +9 more
semanticscholar +1 more source
Skull Base, 2006 To report the outcomes of surgical treatment of vagal paragangliomas and to define a management protocol.A retrospective case series.Sixteen consecutive patients with vagal paragangliomas managed by surgical resection using a cervicoparotid approach and pericapsular dissection using microsurgical techniques between 1990 and 2003.All patients either had
Zanoletti, Elisabetta, Mazzoni, Antonio
openaire +3 more sources
Imaging of Pheochromocytoma and Paraganglioma
Journal of Nuclear Medicine, 2021 Imaging plays a critical role in the management of pheochromocytomas and paragangliomas and often guides treatment. The discovery of susceptibility genes associated with these tumors has led to better understanding of clinical and imaging phenotypes ...
J. Carrasquillo +6 more
semanticscholar +1 more source
Clinical Case Reports, 2022 Abstract Paragangliomas are rare tumors of the neuroendocrine system that form near certain blood vessels (paraaortic and carotid) and nerves, often presenting heterogeneous parenchyma and displaying strong contrast enhancement on computed tomography.
Romeo Thierry Yehouenou Tessi +3 more
openaire +3 more sources