Results 101 to 110 of about 45,090 (245)
Pheochromocytoma mimicking acute myocarditis
: Pheochromocytoma, a relatively rare (0.1-0.8% of hypertensives), catecholamine-secreting tumor, is almost always lethal unless recognised and appropriately treated.
Kawecka-Jaszcz, Kalina +2 more
core +1 more source
Adrenal Primary Ganglioneuroblastoma Presenting in Adulthood: A Case Report
ABSTRACT Introduction Ganglioneuroblastoma is a rare neuroblastic tumor derived from embryonic neural crest cells, composed of mature gangliocytes and immature neuroblasts. Although most neuroblastic tumors present in children and commonly involve the adrenal glands, adrenal ganglioneuroblastoma is rare in adults, with only 25 previously reported cases.
Keiichiro Yasuda +8 more
wiley +1 more source
Systemic Steroid Application Caused Sudden Death of a Patient with Sudden Deafness
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 +4 more
doaj +1 more source
Integrative analysis of neuroblastoma and pheochromocytoma genomics data
Background Pheochromocytoma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. We have performed a large-scale in silico analysis of altogether 1784 neuroblastoma and 531 pheochromocytoma samples to ...
Szabó Peter M +7 more
doaj +1 more source
Childhood neuroblastoma masquerading as pheochromocytoma: case report
Suk-Bae MoonDepartment of Surgery, Kangwon National University Hospital, Kangwon National School of Medicine, Kangwon National University, Chuncheon, South KoreaAbstract: Neuroblastoma is the most common extracranial solid tumor in children.
Moon SB
core
Cardiovascular Manifestations of Pheochromocytoma
Pheochromocytomas are rare endocrine tumors that can have a significant impact on a variety of organ systems, including the cardiovascular system. Although the pathophysiology is not completely understood, pheochromocytomas exert their effects through ...
Poste, J +9 more
core +1 more source
Ruptured Abdominal Aortic Aneurysm as the Initial Manifestation of Undiagnosed Pheochromocytoma
ABSTRACT Introduction Pheochromocytoma is a rare catecholamine‐secreting tumor that can cause severe cardiovascular complications. Its association with ruptured abdominal aortic aneurysm is extremely rare. Case Presentation A 57‐year‐old man with no significant medical history presented with sudden abdominal pain and hemorrhagic shock.
Kyotaro Fukuta +9 more
wiley +1 more source
Pheochromocytomas and Paragangliomas (PGL) form the group of paraganglial tumours which can occur in any paraganglia from the skull base to the pelvic floor. The terminology is not uniform. While the World Health Organization (WHO) applies pheochromocytoma exclusively to adrenal tumours, many clinicians use the term pheochromocytoma also for extra ...
Erlic, Zoran, Neumann, Hartmut P. H.
openaire +3 more sources
Spontaneous adrenal pheochromocytoma rupture complicated by intraperitoneal hemorrhage and shock
MEN2A is a hereditary syndrome characterized by medullary thyroid carcinoma, hyperparathyroidism, and pheochromocytoma. Classically patients with a pheochromocytoma initially present with the triad of paroxysmal headaches, palpitations, and diaphoresis ...
Kwasnik Edward +4 more
doaj +1 more source
ABSTRACT Alzheimer's disease (AD) is a debilitating neurodegenerative condition characterized by progressive cognitive impairment, memory deterioration, and neuronal dysfunction. Its complex pathophysiology involves multiple interlinked processes, including amyloid‐β (Aβ) aggregation, tau hyperphosphorylation, oxidative stress, neuroinflammation ...
Amandeep Thakur +6 more
wiley +1 more source

