Results 121 to 130 of about 73,068 (324)
Review of Pediatric Pheochromocytoma and Paraganglioma
Frontiers in Pediatrics, 2017 Pheochromocytoma (PCC) and paraganglioma (PGL) are rare chromaffin cell tumors which secrete catecholamines and form part of the family of neuroendocrine tumors.
R. Bholah, T. Bunchman
semanticscholar +1 more source
Radiogenomics: Current Understandings and Future Perspectives
MedComm, Volume 7, Issue 2, February 2026.Radiogenomics links imaging phenotypes with genetic variations, offering potential for comprehensive understanding, cost‐effective diagnosis, and prognosis prediction to advance personalized medicine. However, its clinical application remains limited by several challenges.
Xinyu Zhang +8 more
wiley +1 more source
OR12-5 | LBSAT57 Long-term Follow-Up of Pheochromocytoma/Paraganglioma (PPGL) after first diagnosis: a retrospective single-center study of 173 patients [PDF]
, 2022 Christoph Krall +2 more
openalex +1 more source
Update on Modern Management of Pheochromocytoma and Paraganglioma
Endocrinology and Metabolism, 2017 Despite all technical progress in modern diagnostic methods and treatment modalities of pheochromocytoma/paraganglioma, early consideration of the presence of these tumors remains the pivotal link towards the best possible outcome for patients.
J. Lenders, G. Eisenhofer
semanticscholar +1 more source
Antiangiogenic therapies for pheochromocytoma and paraganglioma.
Endocrine-Related Cancer, 2020 Metastatic pheochromocytomas and paragangliomas are rare, highly vascular tumors that spread primarily to the lymph nodes, skeletal tissue, lungs, and liver. Tumor morbidity is related to their size, location, hormonal activity, vascular nature, and rate
C. Jimenez +2 more
semanticscholar +1 more source
European Journal of Neurology, Volume 33, Issue 2, February 2026.No significant differences were observed at any stage of the RCVS course between patients and controls. Systemic arterial stiffness, as assessed by PWV, remained normal and stable throughout the course of RCVS. No systemic complication has been detected during the RCVS course.
Pacôme Constant dit Beaufils +7 more
wiley +1 more source
Duodenal gangliocytic paraganglioma, a rare entity among GEP-NET: a case report with immunohistochemical and molecular study [PDF]
, 2014 Gastroenteropancreatic neuroendocrine tumors are the most incident neuroendocrine tumors. In the new WHO classification (2010) the embryological derivation of each neoplastic entity is one of the most important parameters. Gangliocytic Paraganglioma is a
Alessia Pelella +7 more
core +2 more sources
Experimental Physiology, Volume 111, Issue 2, Page 539-555, 1 February 2026.Abstract Recent studies highlight the important roles of cuproptosis in cancer cells. However, the roles of the cuproptosis‐related genes (CRGs) in different cancers are still not fully understood. Comprehensive analysis was performed using open‐source bioinformatic platforms to disclose the expression profiles, prognostic significance, genomic and ...
Xinyu Ge +10 more
wiley +1 more source
A Rare Case: Sporadic Bladder Paraganglioma
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2013 Paraganglioma is a rare tumor which originates from paraganglia tissue from neural crest. Bladder paraganglioma is suggested to be from crommaffin cells by the remains of the embryological cells.
Hakan Ercil +5 more
doaj
SAGE Open Medical Case Reports, 2017 Neurofibromatosis type 1 is a complex, multi-system genetic disorder that is associated with an increased prevalence of pheochromocytoma and paraganglioma compared to the general population, 1.0%–5.7% versus 0.2%–0.6%, respectively.
Joshua M Tate +2 more
doaj +1 more source