Results 81 to 90 of about 48,572 (243)
Feocromocitoma recidivante em gestação: relato de caso e revisão da literatura. [PDF]
, 1998 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Tocoginecologia, Curso de Medicina, Florianópolis ...
Alves, Daniela Salvador
core
CD36‐mediated lipid rewiring in the metabolic adaptation of tumour ecosystems
The FEBS Journal, EarlyView.Nutrient deprivation drives a lipid‐centric shift in tumour metabolic symbiosis and signalling network. CD36 functions as a bidirectional bridge, transferring fatty acids from stromal donors (adipocytes, CAFs) to the ecosystem tumour‐ and microenvironment‐dependently.
Anna Sebestyén +11 more
wiley +1 more source
Laparoscopic management of recurrent pheochromocytoma: A case report
Journal of Minimal Access Surgery, 2016 Recurrence of pheochromocytoma after a total adrenalectomy is uncommon. Such recurrent tumours are mostly managed by the open technique, with very few studies reporting laparoscopic management.
Harshit Garg +3 more
doaj +1 more source
Internal Medicine Journal, EarlyView.Abstract Aims To evaluate the sustained impact of the Endocrine Hypertension Service on primary aldosteronism (PA) diagnosis and management over a subsequent 3‐year period. Background PA is a prevalent yet underdiagnosed cause of secondary hypertension, associated with increased cardiovascular, renal and metabolic risk. Limited awareness, resources and
Minn W. Chow +5 more
wiley +1 more source
Journal of Medical Case Reports, 2017 Background Composite pheochromocytoma/paragangliomas are very rare tumors composed of ordinary pheochromocytoma paragangliomas associated with neurogenic tumors. Several hereditary susceptibility disorders are known to be associated with pheochromocytoma/
Boubacar Efared +6 more
doaj +1 more source
A rare case of Ganglioneuroblastoma Encapsulated in Pheochromocytoma
Acta Medica, 2016 Pheochromocytoma and Ganglioneuroblastoma are separate diseases and a rare combination in which the diagnosis can only be confirmed by pathological examination after tumor excision.
Nathália Vieira Sousa +5 more
doaj +1 more source
Undiagnosed pheochromocytoma presenting as a pancreatic tumor: A case report
Open Medicine, 2020 Pheochromocytoma is a rare catecholamine-producing tumor of the adrenal gland. Patients with known pheochromocytoma undergoing surgery require preoperative treatment with alpha-blockers to reduce the risk of intraoperative complications related to ...
Legocka Malgorzata Emilia +5 more
doaj +1 more source
Bariatric Surgery for Pre-Operative Weight Reduction in a Patient with Pheochromocytoma
, 2019 Objective: Obesity is a predictor of adverse outcomes in patients undergoing adrenalectomy. Pre-adrenalectomy weight reduction is becoming an increasingly common challenge in view of the rising prevalence of obesity.
Haigh, Kate J, Davoren, Peter
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Pathologic Fracture as Primary Presentation of Malignant Pheochromocytoma: A Case Report
Acta Medica Iranica, 2019 Pheochromocytoma is a relatively rare tumor with no age preference. This tumor is usually diagnosed accidentally. Pathologic fracture as the primary presentation of malignant pheochromocytoma is an uncommon presentation.
Azar Fanipakdel +3 more
doaj
Adrenocorticotropic Hormone Secreting Pheochromocytoma Underlying Glucocorticoid Induced Pheochromocytoma Crisis [PDF]
, 2018 Context. Pheochromocytomas are hormone secreting tumors of the medulla of the adrenal glands found in 0.1–0.5% of patients with hypertension. The vast majority of pheochromocytomas secrete catecholamines, but they have been occasionally shown to also ...
Matan Fischer +5 more
core +1 more source