Results 21 to 30 of about 10,214 (238)
Neuromodulation: Technology at the Neural Interface, EarlyView., 2021 Abstract Objectives Acute cerebral ischemia is characterized by several pathological processes evolving during time, which contribute to the final tissue damage. Secondary processes, such as prolonged inflammatory response, impaired mitochondrial function and oxidative stress, are responsible for the progression of brain injury to the peri‐infarct area,
Fioravante Capone +8 more
wiley +1 more source
Open Life Sciences, 2021 A 29-year-old woman presented to the emergency department with the acute onset of palpitations, shortness of breath, and haemoptysis. She reported having an abortion (56 days of pregnancy) 1 week before admission because of hyperthyroidism diagnosis ...
Wang Tao, Xu Qiancheng, Jiang Xiaogan
doaj +1 more source
Intracerebral haemorrhage: A rare presentation of phaeochromocytoma
Journal of Indian Association of Pediatric Surgeons, 2021 Phaeochromocytoma is a rare childhood adrenal medullary catecholamine secreting tumour, arising from the chromaffin cells of the sympathetic origin derived from the neural crest cells. Only a few cases have been reported in the literature so far.
Swati Chhikara +5 more
doaj +1 more source
Phaeochromocytoma Mimicking Scleroderma
International Journal of Endocrinology, 2011 We describe a patient with adrenal phaeochromocytoma who presented with peripheral vasospasm and ischaemia and other manifestations mimicking features of systemic sclerosis, which resolved after resection of the tumor.
Joan Joo-Ching Khoo, Edward John Pratt
doaj +1 more source
Catecholamine-induced cardiomyopathy: an endocrinologist’s perspective
Reviews in Cardiovascular Medicine, 2021 Although many endocrine diseases can be associated with acquired cardiomyopathy and heart failure, conditions except hypothyroidism, hyperthyroidism, phaeochromocytoma-paraganglioma (PPGL), and primary hyperaldosteronism are rare.
Aman Kumar +2 more
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Extra-adrenal composite phaeochromocytoma/neuroblastoma in a 15-month-old child
Journal of Pediatric Surgery Case Reports, 2015 A 15-month-old boy was diagnosed with malignant hypertension caused by a catecholamine excreting retroperitoneal paraganglioma consisting of a composite phaeochromocytoma/differentiating neuroblastoma. After alpha-blockade the tumor was excised.
Tom Monclair +5 more
doaj +1 more source
A laboratóriumi diagnosztika eredményei az elmúlt 20 évben kórismézett 155 phaeochromocytoma/paraganglioma szindrómás beteg adatainak elemzése alapján. [PDF]
, 2015 INTRODUCTION: Laboratory diagnosis of pheochromocytoma-paraganglioma syndrome has been markedly improved during the past two decades. AIM: Retrospective assessment of diagnostic utility of urinary catecholamines and their metabolites as well as serum ...
Balog B +11 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 +1 more
core +2 more sources
International Journal of Clinical Practice, 1990 The recurrence of symptoms and hypertension in a patient who has previously undergone an operation for phaeochromocytoma should alert the physician to the need to investigate for recurrent tumour. Failure to perform complete excision of the adrenal gland containing the tumour may lead to disseminated recurrence.
P H, Rowe +5 more
openaire +2 more sources
Case Reports in Anesthesiology, 2013 Phaeochromocytoma is a catecholamine producing tumour and an uncommon cause of hypertension. We present two cases of relatively asymptomatic individuals, in which previously undiagnosed phaeochromocytoma was unmasked by elective nonadrenal surgical ...
P. C. Johnston +7 more
doaj +1 more source