Results 31 to 40 of about 6,532 (206)

Secondary hypertension: A rare cause

open access: yesIndian Journal of Endocrinology and Metabolism, 2011
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]

open access: yes, 2014
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]

open access: yes, 2017
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]

open access: yesJournal of Veterinary Diagnostic Investigation, 2013
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

Functional extra-adrenal paraganglioma of the retroperitoneum giving thoracolumbar spine metastases after a five-year disease-free follow-up: a rare malignant condition with challenging management

open access: yesThe Pan African Medical Journal, 2017
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

Paranglioma de fosa nasal

open access: yesRevista Portuguesa Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, 1969
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]

open access: yes, 2017
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

Concurrent nonfunctional paraganglioma of the retroperitoneum and urinary bladder: A case report with literature review

open access: yesIndian Journal of Radiology and Imaging, 2015
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

open access: yesRadiology and Oncology, 2021
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]

open access: yes, 2014
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

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