Results 71 to 80 of about 40,494 (191)

Epidemiologic Profile and Clinical Outcomes of Patients with Pheochromocytoma at the University of the Philippines - Philippine General Hospital (UP-PGH)

Journal of the ASEAN Federation of Endocrine Societies
Objective. This study aims to describe the epidemiologic profile and determine the clinical outcomes of patients with pheochromocytoma at the University of the Philippines Philippine General Hospital (UP-PGH). Methodology.
Edrome Hernandez, Cecilia Jimeno, Elizabeth Paz-Pacheco   +2 more
doaj   +1 more source

Laparoscopic management of recurrent pheochromocytoma: A case report

Journal of Minimal Access Surgery, 2016
Recurrence of pheochromocytoma after a total adrenalectomy is uncommon. Such recurrent tumours are mostly managed by the open technique, with very few studies reporting laparoscopic management.
Harshit Garg, Manpreet Uppal, Sreesanth Kelu Sreedharan, Sandeep Aggarwal   +3 more
doaj   +1 more source

Bidirectional Ventricular Tachycardia due to Pheochromocytoma: A Case Report

Annals of Noninvasive Electrocardiology
Pheochromocytoma, a type of neuroendocrine tumor, can cause numerous symptoms and signs similar to those of other clinical conditions, with the classic triad being palpitations, headache, and diaphoresis.
Gui‐yang Li, Man‐Xin Lin, Fa‐Guang Zhou, Qiang Li   +3 more
doaj   +1 more source

Bilateral pheochromocytoma with ganglioneuroma component associated with multiple neuroendocrine neoplasia type 2A: a case report

Journal of Medical Case Reports, 2017
Background Composite pheochromocytoma/paragangliomas are very rare tumors composed of ordinary pheochromocytoma paragangliomas associated with neurogenic tumors. Several hereditary susceptibility disorders are known to be associated with pheochromocytoma/
Boubacar Efared, Gabrielle Atsame-Ebang, Soufiane Tahirou, Khalid Mazaz, Nawal Hammas, Hinde El Fatemi, Laila Chbani   +6 more
doaj   +1 more source

Undiagnosed pheochromocytoma presenting as a pancreatic tumor: A case report

Open Medicine, 2020
Pheochromocytoma is a rare catecholamine-producing tumor of the adrenal gland. Patients with known pheochromocytoma undergoing surgery require preoperative treatment with alpha-blockers to reduce the risk of intraoperative complications related to ...
Legocka Malgorzata Emilia, Toutounchi Sadegh, Pogorzelski Ryszard, Krajewska Ewa, Celejewski Krzysztof, Galazka Zbigniew   +5 more
doaj   +1 more source

ST-Segment Elevation Myocardial Infarction Related to Potential Spontaneous Coronary Thrombosis in Pheochromocytoma Crisis

Frontiers in Endocrinology, 2020
Pheochromocytoma crisis is a rare and possibly fatal emergency. Hypersecreted catecholamines may result in myocardial injury via its direct toxic effect on cardiomyocytes or mediating vasoconstriction which will reduce coronary blood flow in this special
Fei Chen, Mingxia Zheng, Xi Li, Yong Peng, Mao Chen   +4 more
doaj   +1 more source

Absence of an embryonic stem cell DNA methylation signature in human cancer. [PDF]

, 2019
BackgroundDifferentiated cells that arise from stem cells in early development contain DNA methylation features that provide a memory trace of their fetal cell origin (FCO). The FCO signature was developed to estimate the proportion of cells in a mixture
Christensen, Brock C, Kelsey, Karl T, Koestler, Devin C, Salas, Lucas A, Wiencke, John K, Zhang, Ze   +5 more
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Recurrent Catecholamine-Induced Cardiomyopathy in a Patient With a Pheochromocytoma [PDF]

, 2009
Pheochromocytomas presents with variable clinical manifestations. Cardiomyopathy caused by a pheochromocytoma is well known. We report the case of a 62-year-old woman with recurrent left ventricular dysfunction, who was subsequently found to have a ...
Attar, Copetti, Dong Heon Yang, Hong, Hun Sik Park, Jae Eun Jun, Jae Hee Kim, Mann, Sanchez-Recalde, Sang Hyuk Lee, Sardesai, Se Yong Jang, Shung Chull Chae, Sun Hee Park, Szakacs, Takeno, Takizawa, van de Walle, Wee Hyun Park, Yongkeun Cho   +19 more
core   +2 more sources

Systemic Steroid Application Caused Sudden Death of a Patient with Sudden Deafness

Case Reports in Otolaryngology, 2013
A 63-year-old man, who was diagnosed with sudden sensorineural hearing loss (SSHL), showed severe hypertension 10 hours after prednisolone administration. Subsequently, the patient suddenly died due to pulmonary edema.
Eriko Ogino-Nishimura, Takayuki Nakagawa, Ichiro Tateya, Harukazu Hiraumi, Juichi Ito   +4 more
doaj   +1 more source

Characterisation of ERK distribution and activity in rat pheochromocytoma cells : a thesis presented in partial fulfilment of the requirements for the degree of Master of Science in Molecular Biology at Massey University [PDF]

, 1998
Nerve growth factor (NGF) binds to the NGF receptor, TrkA, at the tips of nerve cell axons, sending a signal that prevents programmed cell death and causes survival, growth, and differentiation of the nerve cell.
MacCormick, Matthew Edgar
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