Results 31 to 40 of about 51,236 (315)

Simultaneous Contralateral Vestibular Schwannoma and Middle Ear Paraganglioma Tumor [PDF]

, 2017
To the best of our knowledge, only 2 cases of a simultaneous contralateral vestibular schwannoma (VS) and middle ear paraganglioma (MEP) have previously been reported in literature.
Barbara, M, Covelli, E, Fabiani, V, Filippi, C, Monini, S, Trasimeni, Guido, Volpini, L   +6 more
core   +1 more source

Intrapericardial paraganglioma

Journal of the Belgian Society of Radiology, 2014
Background: A 38-year-old woman presented for a follow-up CT of the neck and the chest. She had a history of familial disease and neck surgery 11 years earlier. Physical examination and laboratory results were normal. An intrapericardial lesion was suspected on a thoracic MR examination 5 years earlier. Unenhanced CT scan, contrast-enhanced CT scan and
Teodorescu, Marian, Coche, Emmanuel, Ghaye, Benoît   +2 more
openaire   +6 more sources

Treatment responses to antiangiogenetic therapy and chemotherapy in nonsecreting paraganglioma (PGL4) of urinary bladder with SDHB mutation: a case report [PDF]

, 2018
Paraganglioma (PGL) is a rare neuroendocrine tumor. Currently, the malignancy is defined as the presence of metastatic spread at presentation or during follow-up.
Aschelter, Am, Capriotti, G, Cerquetti, L, Lardo, P, Marchetti, P, Matarazzo, I, Nardone, Mr, Petrangeli, E, Schiavi, F, Stigliano, A, Toscano, V   +10 more
core   +1 more source

Metastatic paraganglioma

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, Andrew Mallia, James Degaetano, Paul John Cassar   +3 more
semanticscholar   +1 more source

The genetics of paragangliomas

European Annals of Otorhinolaryngology, Head and Neck Diseases, 2012
Over the last decade, it has been clearly established that one-third of all paragangliomas are genetically determined. Genetic testing, guided by the family history and clinical findings, must now be proposed to all subjects undergoing surgery for head and neck paraganglioma. When a mutation is identified on one of the susceptibility genes (SDHD, SDHB,
N. Abermil, N. Abermil, Alexandre Buffet, Alexandre Buffet, Judith Favier, Judith Favier, Anne-Paule Gimenez-Roqueplo, Anne-Paule Gimenez-Roqueplo, N. Burnichon   +8 more
openaire   +3 more sources

Paraganglioma presenting as hypertension during pregnancy, proteinuria, thrombocytosis, and diabetes mellitus: a case report

Journal of Medical Case Reports, 2021
Background Paraganglioma is a very rare cause of pregnancy-induced hypertension. The objective of this case report is to present a case of paraganglioma presented during pregnancy and missed.
Ramjan Sanas Mohamed, Charles Naveenan Antonypillai, Harishanthi Mahendran   +2 more
doaj   +1 more source

Routine genetic screening with a multi-gene panel in patients with pheochromocytomas [PDF]

, 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, Grossman, Ashley B., Isidori, Andrea, Jafar mohammadi, Bahram, Mihai, Radu, Pal, Aparna, Sadler, Greg, Sbardella, Emilia, Shine, Brian   +8 more
core   +1 more source

Integrative multi-omics analysis identifies a prognostic miRNA signature and a targetable miR-21-3p/TSC2/ mTOR axis in metastatic pheochromocytoma/ paraganglioma [PDF]

, 2019
Artículo escrito por un elevado número de autores, solo se referencian el que aparece en primer lugar y los autores pertenecientes a la UAMPheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that present variable outcomes.
Alvarez - Escola, Cristina, Calsina, Bruna   +1 more
core   +2 more sources

Successful Surgical Management of a Coincidence of Three‐Vessel Coronary Artery Disease, Severe Carotid Atherosclerosis, and Carotid Paraganglioma: A Case Report and Literature Review [PDF]

Clin Case Rep
The patient was diagnosed with three significant pathologies, which were managed successfully in a single surgery. ABSTRACT Screening for carotid atherosclerosis is mandatory before coronary artery bypass graft (CABG). Incidental pathologies, such as carotid paraganglioma, may be discovered rarely, complicating management.
Ebrahimi P, Akbari T, Nozheh A, Nasrollahizadeh A, Javankiani S, Ramezani P, Mandegar M, Doshi S, Shahid F.   +8 more
europepmc   +2 more sources

Hypoglossal schwannoma masquerading as a carotid body tumor. [PDF]

, 2012
Study Objective. To describe the clinical presentation, evaluation, and treatment of a hypoglossal schwannoma. Methods. We report an unusual case of a hypoglossal schwannoma presenting as a pulsatile level II neck mass at the bifurcation of the external ...
Abie H. Mendelsohn, Article Id, Douglas R. Sidell, Keith E. Blackwell, Matthew K. Lee   +4 more
core   +1 more source