Results 21 to 30 of about 73,068 (324)

Non‐Functional Paraganglioma of the Urinary Bladder: A Rare Cause of Bladder Tumor [PDF]

open access: yesIJU Case Rep
ABSTRACT Introduction Paragangliomas of the urinary bladder (PUBs) are rare neuroendocrine tumors, representing less than 0.06% of all bladder neoplasms. While most are functional and associated with catecholamine excess, approximately 15% are non‐functional, often presenting asymptomatically and discovered incidentally.
Wainstein M   +4 more
europepmc   +2 more sources

Targeted therapies in Pheochromocytoma and Paraganglioma.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2022
Molecular targeted therapy plays an increasingly important role in the treatment of metastatic pheochromocytomas and paragangliomas (PPGLs), which are rare tumors but remain difficult to treat.
Katharina Wang   +5 more
semanticscholar   +1 more source

Coronary paraganglioma [PDF]

open access: yesClinical Cardiology, 1982
AbstractThe clinical, angiographic, and anatomical features of an uncommon primary cardiac tumor, a paraganglioma, are presented. The angiographic appearance appears unique. These tumors are slow growing and troublesome primarily because of their firm adherence to underlying cardiac structures. Treatment is complete surgical excision.
B, Levi, A S, Cain, W E, Dorzab
openaire   +2 more sources

High-Specific-Activity-131I-MIBG versus 177Lu-DOTATATE Targeted Radionuclide Therapy for Metastatic Pheochromocytoma and Paraganglioma

open access: yesClinical Cancer Research, 2021
Targeted radionuclide therapies (TRT) using 131I-metaiodobenzylguanidine (131I-MIBG) and peptide receptor radionuclide therapy (177Lu or 90Y) represent several of the therapeutic options in the management of metastatic/inoperable pheochromocytoma ...
Abhishek Jha   +24 more
semanticscholar   +1 more source

Natural History and Management of Familial Paraganglioma Syndrome Type 1: Long-Term Data from a Large Family [PDF]

open access: yes, 2020
Head and neck paragangliomas are the most common clinical features of familial paraganglioma syndrome type 1 caused by succinate dehydrogenase complex subunit D (SDHD) mutation. The clinical management of this syndrome is still unclear.
Cantisani, Vito   +12 more
core   +1 more source

Intrapericardial paraganglioma [PDF]

open access: yesEuropean Journal of Cardio-Thoracic Surgery, 1996
We describe the case of an intrapericardial pheochromocytoma located in the anterior surface of the heart and spreading over the pulmonary trunk. Under cardiopulmonary bypass (CPB) the tumor was removed. "En bloc" resection of the anterior wall of the right ventricular infundibulum and the pulmonary trunk was performed, with implantation of a fresh ...
J, Casanova   +5 more
openaire   +2 more sources

European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
Some 5861 patients undergoing first‐time surgery for sporadic primary hyperparathyroidism were registered in the Eurocrine® database between 2015 and 2018. The use of intraoperative parathyroid hormone measurement decreased the risk of conversion and persistent hypercalcaemia.
A. Bergenfelz   +3 more
wiley   +1 more source

Unrecognised adrenergic symptoms and the delayed diagnosis of urinary bladder paraganglioma [PDF]

open access: yesVojnosanitetski Pregled, 2015
Introduction. Paraganglioma is a rare neuroendocrine neoplasm that may arise from the extra-adrenal autonomic paraganglia. Urinary bladder paraganglioma is typically presented as repeated episodes of palpitations, headache or blood pressure rise
Dragović Tamara   +6 more
doaj   +1 more source

An Extra-adrenal Pheochromocytoma Presenting as Malignant Hypertension-A Report of two cases [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Malignant hypertension is a complication of hypertension characterized by elevated blood pressure (200mm/140mm Hg), is considered a medical emergency and is rarely secondary to paraganglioma.
Mahesh Kumar U   +4 more
doaj   +1 more source

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

open access: yes, 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   +6 more
core   +1 more source

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