Results 31 to 40 of about 6,532 (206)
Secondary hypertension: A rare cause
A 13-year-old, previously asymptomatic girl was admitted with features of tuberculous meningitis. She was found to be hypertensive and further investigations revealed an extra-adrenal paraganglioma.
Mary Grace +3 more
doaj +1 more source
Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations [PDF]
The SDHD gene encodes a subunit of the mitochondrial tricarboxylic acid cycle enzyme and tumor ...
Bayley, J.P. (Jean-Pierre) +12 more
core +4 more sources
Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report [PDF]
BackgroundRecent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). The clinical characteristics of hereditary PPGL are varying among the types of mutational genes.
Adachi Yayoi +13 more
core +2 more sources
Extra-adrenal retroperitoneal paraganglioma in a dog [PDF]
An extra-adrenal retroperitoneal paraganglioma was observed in a 10.5-year-old male Boxer dog. Additionally, the dog had an aortic base tumor, multiple thyroid adenomas, multiple testicular interstitial cell tumors, bilateral nodular adrenal cortical hyperplasia, and parathyroid gland hyperplasia.
Marcia R S, Ilha, Eloise L, Styer
openaire +2 more sources
Paragangliomas are benign neoplasms that arise from the autonomic nervous system and the associated paraganglia. Although benign, they have been shown to possess metastatic potential.
Stylianos Kapetanakis +5 more
doaj +1 more source
EI paraganglioma es un tumor neuroendocrino que en un 5-10% de los casos se presenta en una localización extra-adrenal. Presentamos el caso en una paciente de cincuenta y tres anos con un paraganglioma localizado en la fosa nasal, siendo esta ...
Pilar Navarro Paule +5 more
doaj +1 more source
Routine genetic screening with a multi-gene panel in patients with pheochromocytomas [PDF]
PURPOSE: Several new gene mutations have been reported in recent years to be associated with a risk of familial pheochromocytoma. However, it is unclear as to whether extensive genetic testing is required in all patients. METHODS: The clinical data
Cranston, Treena +8 more
core +1 more source
Paragangliomas are the neuroendocrine tumors which arise from the chromaffin cell. Tumors arising from the adrenal medulla are known as pheochromocytomas, while others originating from the extra-adrenal site are known as extra-adrenal paragangliomas ...
Poonam Sherwani +4 more
doaj +1 more source
Bladder paraganglioma: CT and MR imaging characteristics in 16 patients
Bladder paraganglioma (BPG) is a rare extra-adrenal pheochromocytoma with variable symptoms and easy to be misdiagnosed and mishandled. The aim of the study was to document the imaging features of BPG using computed tomography (CT) and magnetic resonance
Zhang Jing +6 more
doaj +1 more source
Mapping of succinate dehydrogenase losses in 2258 epithelial neoplasms. [PDF]
Losses in the succinate dehydrogenase (SDH) complex characterize 20% to 30% of extra-adrenal paragangliomas and 7% to 8% of gastric GISTs, and rare renal cell carcinomas.
Biernat, Wojciech +9 more
core +1 more source

