Results 61 to 70 of about 6,550 (210)
Functional paraganglioma of the bladder: Both radiographic‐negative and laboratory‐negative case
IJU Case Reports, 2019 Introduction Paraganglioma has been determined to be an extra‐adrenal pheochromocytoma. Paraganglioma of the bladder is a rare entity, accounting for 0.06% of all bladder tumors.
Rumiko Sugimura +9 more
doaj +1 more source
Primary non-functioning paraganglioma of liver: A rare tumour at an unusual location [PDF]
, 2011 Pheochromocytomas are rare tumours, 22% of which are extra-adrenal and are known as paragangliomas. We report a case of a young male with non-functioning paraganglioma of the liver; a very uncommon primary site.
Ahmed, Arsalan +3 more
core +1 more source
Pheochromocytoma presenting as recurrent urinary tract infections : a case report [PDF]
, 2011 Introduction Pheochromocytomas are rare, potentially fatal, neuroendocrine tumors of the adrenal medulla or extra-adrenal paraganglia. Their clinical presentation varies greatly from the classic triad of episodic headache, diaphoresis and tachycardia to ...
Roisin T Dolan +3 more
core +2 more sources
Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]
, 2018 Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev +6 more
core +1 more source
Pheochromocytoma and Extra-adrenal Paraganglioma: Updates
Archives of Pathology & Laboratory Medicine, 2008 Abstract Context.—Advances in genetics and gene expression profiling have led to new ways of thinking about the pathobiology of pheochromocytoma and extra-adrenal paraganglioma. These developments are concurrent with the publication and dissemination of the 2004 World Health Organization bluebook on pathology and genetics of endocrine ...
openaire +2 more sources
An unusual combination of extra-adrenal pheochromocytoma and arteriovenous malformation of the ureter in a young adult [PDF]
, 2013 We present a case of a 24-year-old gentleman who presented with painless pan haematuria for 2 weeks. During the workup, he was diagnosed to have a retrocaval mass after a CT scan while cystoscopy revealed a polypoidal pulsating lesion in the left ureter.
Abbas, Farhat +3 more
core +2 more sources
Laparoscopic management of paraganglioma in a pregnant woman: a case report
International Brazilian Journal of UrologyIntroduction: Paraganglioma is an extremely rare catecholamine-producing tumor during pregnancy. Paraganglioma carries high risks of fetal and maternal mortality during pregnancy.
Mohammad Hadi Radfar +3 more
doaj +1 more source
A case of familial phaechromocytoma- was it? [PDF]
, 2015 With advancement in genetic studies, familial phaeochromocytoma (PCC) and paraganglioma (PGL) are increasingly being recognized. Characteristically, correlations exist between genotypes and clinical and biochemical phenotypes.
Mazlan, Khalidah +2 more
core
Iatreia, 2014 Paragangliomas are tumors that derive from chromaffin cells, which originate in the neural crest. This gives them the ability to secrete catecholamines, hormones and peptides.
Gómez Galán, Sebastian +3 more
doaj
Indian Journal of Pathology and MicrobiologyParagangliomas are rare tumors arising from extra adrenal chromaffin cells. The incidence of primary pulmonary paraganglioma is even less. As new cases are added to the literature, clinical and radiological features become more diverse.
Busra Ozdemir Ciflik +3 more
doaj +1 more source