Results 11 to 20 of about 36,081 (192)
IJU Case Reports, 2022 Introduction SDH Gene mutation is known to be a common cause of pheochromocytoma/paraganglioma and renal cell carcinoma. Here, we report a case of succinate dehydrogenase B‐deficient paraganglioma, which has a high risk of metastasis and recurrence ...
Yoshitomo Yamaguchi +9 more
doaj +1 more source
European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism
BJS (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
BMC Anesthesiology, 2020 Background Paraganglioma can be found in a wide range of locations. However, paraganglioma in the posterior mediastinum is rare. An unexpected paraganglioma located in the posterior mediastinum was found during surgery.
Zhuqing Yang, Qinye Shi, Fangping Bao
doaj +1 more source
Unrecognised adrenergic symptoms and the delayed diagnosis of urinary bladder paraganglioma [PDF]
Vojnosanitetski 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]
Journal 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
An ectopic paraganglioma supplied by the subclavian artery in the right supraclavicular fossa
Journal of Vascular Surgery Cases and Innovative Techniques, 2019 Paragangliomas are rare and highly vascularized neuroendocrine tumors originating from neural crest-derived paraganglionic tissue surrounding the autonomic nerve.
Yang Wang, MD +4 more
doaj +1 more source
Frontiers in Endocrinology, 2020 Ectopic adrenocorticotropic hormone (ACTH) syndrome caused by paraganglioma is extremely rare. It usually accompanied by high or normal plasma ACTH level.
Siyue Liu +4 more
doaj +1 more source
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 +2 more
doaj +1 more source
Pheochromocytoma and Paraganglioma [PDF]
, 2010 Pheochromocytoma is a very special kind of tumor full of duplicity. On the one hand it represents its own microworld with unique clinical, biochemical and pathological features, while on the other it constitutes a tremendously significant part of whole body system, playing a vital role for practically every organ system. It has a very special character
Vitaly, Kantorovich, Karel, Pacak
openaire +2 more sources
Clinical 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