Results 21 to 30 of about 42,772 (234)

TRACHEAL AND SUBGLOTTIC PARAGANGLIOMA, A CASE REPORT [PDF]

Acta Medica Iranica, 2005
In the head and neck region, tracheal and larynx paragangliomas are much less common and subglottic paragangliomas have been rarely reported. Less than 60 cases with larynx paraganglioma and a few cases with ‎trachea paraganglioma have been reported ...
K. Khalkhali, A. Nadimi-Tehrani, N. Yazdani A. Azizi   +2 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, S. van Slycke, Ö. Makay, L. Brunaud   +3 more
wiley   +1 more source

Immunological Features of Neuroendocrine Neoplasms and Adrenal Tumors. [PDF]

Cancer Med
ABSTRACT Neuroendocrine neoplasms, which occur throughout the human body, as well as adrenocortical carcinoma and pheochromocytoma, which originate in the adrenal gland, are primarily classified as rare malignancies. Immunotherapy, including immune checkpoint inhibitors (ICIs), is generally not incorporated into the standard care protocols for these ...
Ohmoto A, Takahashi S, Kitano S.
europepmc   +2 more sources

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, Pankaj Pande, Savita SS, Ashwin PK, Balasaheb Ramling Yelikar   +4 more
doaj   +1 more source

Clinicoradiological manifestations of paraganglioma syndromes associated with succinyl dehydrogenase enzyme mutation. [PDF]

, 2011
BACKGROUND: Paragangliomas are rare tumours derived from the autonomic nervous system that have increasingly been recognised to have a genetic predisposition.
Hodgson, S, Brendan Barber, Khan, S, Bano, G, Mark Ingram, Ingram, M, Vlahos, I, Gul Bano, Barber, B, Shirley Hodgson, Ioannis Vlahos, Sameer Khan   +11 more
core   +2 more sources

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, Zhen Liu, MD, Chong Lian, MD, Shenming Wang, PhD, Jinsong Wang, PhD   +4 more
doaj   +1 more source

Adrenocorticotropic Hormone-Producing Paraganglioma With Low Plasma ACTH Level: A Case Report and Review of the Literature

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, Zhelong Liu, Fuqiong Chen, Weijie Xu, Gang Yuan   +4 more
doaj   +1 more source

Paraganglioma presenting as hypertension during pregnancy, proteinuria, thrombocytosis, and diabetes mellitus: a case report

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, Charles Naveenan Antonypillai, Harishanthi Mahendran   +2 more
doaj   +1 more source

Paraganglioma vesical en edad pediátrica: reporte de caso

, 2023
Introduction: Paraganglioma is a neuroendocrine tumor of unusual presentation in the pediatric age. These are neoplasms that produce, store and secrete catecholamines or their respective metabolites, being an uncommon cause of secondary arterial ...
Caviedes R., Vanessa, Mora Castillo, Dayana, Vargas Rodríguez, Ledmar Jovanny, Mojica Walteros, Carlos Manuel   +3 more
core   +1 more source

Succinate dehydrogenase (SDH)-deficient renal carcinoma:a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients [PDF]

, 2014
Succinate dehydrogenase (SDH)-deficient renal carcinoma has been accepted as a provisional entity in the 2013 International Society of Urological Pathology Vancouver Classification.
Sedivcová, Monika, Yu, Darryl, Papathomas, Thomas, Niemeijer, Nicolasine D., Przybycin, Christopher, Nicoll, Katherine D, Paik, Julie, Miettinen, Markku, Yong, Jim L., Kedziora, Andrew, Andresen, Per Arne, Hes, Ondrej, Toon, Christopher W., Robinson, Bruce G, Corssmit, Eleonora P M, Michal, Michal, Chou, Angela, Hills, Kirsten, Nicoll, Katherine D., Clarkson, Adele, Clifton-bligh, Roderick J., Yong, Jim L, Maclean, Fiona, Yilmaz, Asli, Vlatkovic, Ljiljana, Niemeijer, Nicolasine D, Hartmann, Arndt, Sibony, Mathilde, Agaimy, Abbas, McKenney, Jesse K, Robinson, Bruce G., Van Leenders, Geert J.l.h., Chow, Chung W., Sioson, Loretta, Mckenney, Jesse K., Corssmit, Eleonora P.m., Tan, Puay Hoon, van Leenders, Geert J L H, Yakirevich, Evgeny, Trpkov, Kiril, Benn, Diana E., Gill, Anthony J., Chow, Chung W, Watson, Nicole, Fleming, Stewart, Magi-Galluzzi, Cristina, Clifton-Bligh, Roderick J   +46 more
core   +1 more source