Results 41 to 50 of about 4,742 (176)
Vascular Supply of Laryngeal Paragangliomas: Case Report and Systematic Review
ABSTRACT Objective Laryngeal paragangliomas are rare, highly vascularized, neuroendocrine tumors. Although surgical resection of these vascular neoplasms is associated with a known risk of significant hemorrhage, the vascular supply of laryngeal paragangliomas has been poorly characterized. Data Sources MEDLINE Ovid, Embase, Scopus, and Google Scholar.
Jane Y. Tong +3 more
wiley +1 more source
Hypertension secondary to paraganglioma: case report and review of the literature
We report the case of a 25 year-old man with a history of transient stroke during adolescence, and longstanding uncontrolled hypertension who presented with palpitations, diaphoresis and headache.
Rubio-Marín, Andrea Constanza +3 more
doaj +1 more source
Extra- Adrenal Silent Retroperitoneal Paraganglioma: Report of a Rare Case [PDF]
Extra- adrenal retroperitoneal paragangliomas are extremely rare neuroendocrine neoplasms with an incidence of 2-8 per million. They arise from embryonic neural crest cells and are composed mainly of chromaffin cells located in the para- aortic ...
Hemalatha. A. L +4 more
doaj +1 more source
A 30-year-old woman with severe hypertension was admitted to the hospital with a history of headache, palpitations, and diaphoresis following sexual intercourse.
Nicola Di Daniele +7 more
doaj +1 more source
Quality of Life After Surgical Treatment of Head and Neck Paragangliomas
ABSTRACT Background Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors and often arise in the head and neck. Due to their localization, the tumor and its surgical treatment pose a risk for cranial nerve impairments. Few studies have focused on the health‐related quality of life (HRQOL) in patients with HNPGLs and their relation to ...
Christina Sauter +5 more
wiley +1 more source
Utility of immunohistochemical staining for the diagnosis of Extra-adrenal mediastinal paraganglioma
Extra-adrenal, mediastinal paraganglioma are rare tumors that origin from sympathetic ganglia. Common diagnostic steps include CT, MRI and PET-Scan.
Isabella B. Metelmann +3 more
doaj +1 more source
Metoclopramide‐Induced Pheochromocytoma Crisis: A Case Report and Literature Review
ABSTRACT Pheochromocytoma is a catecholamine‐secreting neuroendocrine tumor originating in the adrenal medulla. In patients with pheochromocytoma, paroxysmal over‐secretion of catecholamines can be triggered by various medications, including the commonly used antiemetic metoclopramide.
Yuki Yamanishi +4 more
wiley +1 more source
Coexistence of pheochromocytoma/praganglioma and renal artery stenosis
Renal artery stenosis (RAS) often coexists with pheochromocytoma (Pheo)/paraganglioma (PGL) and often alters the management of patients with Pheo/PGL. We have studied the prevalence of RAS in our Pheo/PGL patients.
Vijaya Sarathi +6 more
doaj +1 more source
Pancreatic paraganglioma mimicking pancreatic neuroendocrine tumor
Extra-adrenal paragangliomas are rare tumors arising from the chromaffin cells of the autonomic nervous system. Retroperitoneal paragangliomas may present as a pancreatic mass.
Arezou Abbasi +2 more
doaj +1 more source
Non‐Functional Paraganglioma of the Urinary Bladder: A Rare Cause of Bladder Tumor
ABSTRACT Introduction Paragangliomas of the urinary bladder (PUBs) are rare neuroendocrine tumors, representing less than 0.06% of all bladder neoplasms. While most are functional and associated with catecholamine excess, approximately 15% are non‐functional, often presenting asymptomatically and discovered incidentally.
Matt Wainstein +4 more
wiley +1 more source

