Results 71 to 80 of about 74,986 (277)
A case of pheochromocytoma presenting with cardiac manifestation: case report
BMC Pediatrics, 2020 Background Pheochromocytomas are rare tumors originating in chromaffin cells which predominantly are located in adrenal glands. Sustained or paroxysmal hypertension (HT) is the most frequent sign of pheochromocytoma.
Akbar Molaei +2 more
doaj +1 more source
UroPrecision, EarlyView.Abstract Background Adrenal tumor is a common condition that often requires adrenalectomy. The objective of this study is to compare the safety and implementation of the enhanced recovery after surgery (ERAS) among patients who received open, laparoscopic and robotic‐assisted operation.
Bingfeng Luo +7 more
wiley +1 more source
Pathologic Fracture as Primary Presentation of Malignant Pheochromocytoma: A Case Report
Acta Medica Iranica, 2019 Pheochromocytoma is a relatively rare tumor with no age preference. This tumor is usually diagnosed accidentally. Pathologic fracture as the primary presentation of malignant pheochromocytoma is an uncommon presentation.
Azar Fanipakdel +3 more
doaj
Giant cystic pheochromocytoma: A silent entity
Urology Annals, 2016 Pheochromocytoma is a catecholamine secreting tumor that originate from chromaffin cells. Usually, it is solid neoplasm of the adrenal medulla, however cystic pheochromocytoma is a rare neuro-endocrine tumour that is frequently asymptomatic and often ...
Amit Gupta +3 more
doaj +1 more source
Ocular muscle metastasis as the initial presentation of a malignant pheochromocytoma: A unique case
Clinical Case Reports, 2020 In this paper, we discuss a unique manifestation of malignant pheochromocytoma, which presented with ocular pain. The histopathological study pointed to a possible pheochromocytoma origin.
Gholamreza Khataminia +6 more
doaj +1 more source
Nerve growth factor nonresponsive pheochromocytoma cells: altered internalization results in signaling dysfunction. [PDF]
, 1992 Variant rat pheochromocytoma (PC12) cells which fail to respond to nerve growth factor (NGF) (PC12nnr5) (Green, S. H., R. E. Rydel, J. L. Connoly, and L. A. Greene. 1986. J. Cell Biol. 102:830-843) bind NGF at both high and low affinity sites.
Bradshaw, RA, Eveleth, DD
core
ERNEST COST action overview on the (patho)physiology of GPCRs and orphan GPCRs in the nervous system
British Journal of Pharmacology, EarlyView.G protein‐coupled receptors (GPCRs) are a large family of cell surface receptors that play a critical role in nervous system function by transmitting signals between cells and their environment. They are involved in many, if not all, nervous system processes, and their dysfunction has been linked to various neurological disorders representing important
Necla Birgül Iyison +15 more
wiley +1 more source
A rare case of Ganglioneuroblastoma Encapsulated in Pheochromocytoma
Acta Medica, 2016 Pheochromocytoma and Ganglioneuroblastoma are separate diseases and a rare combination in which the diagnosis can only be confirmed by pathological examination after tumor excision.
Nathália Vieira Sousa +5 more
doaj +1 more source
British Journal of Pharmacology, Volume 182, Issue 9, Page 1879-1896, May 2025.Abstract Background and Purpose Phentolamine is a non‐selective α‐adrenoreceptor antagonist used to reverse local anaesthesia, for example, during dental procedures when a vasoconstrictor is co‐applied. Phentolamine‐mediated vasodilation leads to faster clearance of injected drugs.
Idil Toklucu +8 more
wiley +1 more source
Kaohsiung Journal of Medical SciencesPheochromocytoma is a tumor that usually originating from adrenal medullary chromaffin cells and producing one or more catecholamines, can manifest as hereditary or sporadic.
Narin Nasiroglu Imga +5 more
doaj +1 more source