Results 41 to 50 of about 50,666 (222)

Preoperative Management of Pheochromocytoma and Paraganglioma

open access: yesFrontiers in Endocrinology, 2020
Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors, characterized by excessive release of catecholamines (CAs), and manifested as the classic triad of headaches, palpitations, profuse sweating, and a variety of other signs and ...
Fang Fang, Li Ding, Qing He, Ming Liu
semanticscholar   +1 more source

Paragangliomas and paraganglioma syndromes

open access: yesLaryngo- rhino- otologie, 2011
GMS Current Topics in Otorhinolaryngology - Head and Neck Surgery; 10:Doc03; ISSN 1865 ...
openaire   +4 more sources

Unsuspected Paraganglioma—Infratemporal Fossa

open access: yesJournal of Neuroanaesthesiology and Critical Care, 2020
Paraganglioma of the infratemporal fossa is exceedingly rare, with no more than a handful of documented cases. Undiagnosed paraganglioma poses a great challenge.
Nikhat Sultana J   +3 more
doaj   +1 more source

Unusually large paraganglioma complicated with successive catecholamine crises: A case report and review of the literature

open access: yesFrontiers in Surgery, 2022
BackgroundParagangliomas are rare neuroendocrine tumors that could secret catecholamines. Hypertension and heart failure caused by the catecholamine crisis are fatal cardiovascular events.
Zhenhui Huang   +5 more
doaj   +1 more source

Prognosis of Malignant Pheochromocytoma and Paraganglioma (MAPP-Prono Study): A European Network for the Study of Adrenal Tumors Retrospective Study.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2019
BACKGROUND Malignant pheochromocytoma and paraganglioma (MPP) are characterized by prognostic heterogeneity. Our objective was to look for prognostic parameters of overall survival (OS) in MPP patients.
S. Hescot   +31 more
semanticscholar   +1 more source

Pheochromocytoma and Paraganglioma: From Epidemiology to Clinical Findings

open access: yesSisli Etfal Hastanesi tip bulteni, 2020
Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors. Pheochromocytomas arise from chromaffin cells in the adrenal medulla, and PGLs arise from chromaffin cells in the ganglia of the autonomic nervous system.
N. Aygun, M. Uludağ
semanticscholar   +1 more source

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen   +23 more
wiley   +1 more source

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

Bladder Paraganglioma

open access: yesJournal of the Belgian Society of Radiology, 2020
Teaching Point: A submucosal bladder wall lesion with high signal on T2-weighted MRI warrants blood and urine analysis to rule out a paraganglioma.
Degrieck, Bert   +2 more
openaire   +5 more sources

Clinical Course and Impact of Breaks in Therapy for Children With Relapsed/Refractory Solid Tumors

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction Pediatric relapsed or refractory (R/R) solid tumors carry a dismal prognosis, and postrelapse patient experiences are not well described. We present postrelapse outcomes, including number of R/R events and subsequent therapy regimens.
Matthew T. McEvoy   +5 more
wiley   +1 more source

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