Results 21 to 30 of about 4,742 (176)
Who can safely discontinue lifelong follow-up among patients with sporadic pheochromocytoma and paraganglioma? [PDF]
Abstract Background Current guidelines recommend at least 10 years of follow‐up for all pheochromocytoma and paraganglioma (PPGL) patients and lifelong monitoring for high‐risk individuals. Nonetheless, data identifying patients who may not require routine lifelong follow‐up are scarce. Methods Among 999 patients with PPGL, 703 who were non‐metastatic,
Park MJ +15 more
europepmc +2 more sources
Anesthetic management of a patient with undiagnosed paraganglioma -a case report- [PDF]
Retroperitoneal paragangliomas are uncommon neuroendocrine tumors which are derived from extra-adrenal paraganglioma with various clinical signs and symptoms.
In Soo Han +4 more
doaj +1 more source
Sudden Death and an Extra-Adrenal Paraganglioma [PDF]
Pheochromocytomas and paragangliomas are a rare cause of sudden death. We present the case of a 34-year-old male who died suddenly. He had been diagnosed as having diabetes mellitus five days previously and was hypertensive. At autopsy he had a 3.5 cm extra-adrenal mass.
Jacqueline L, Parai +1 more
openaire +2 more sources
Pheochromocytoma are catecholamine-producing neuroendocrine tumors that can be adrenal or extra-adrenal (paraganglioma) in origin. The mainstay of definitive therapy is surgical resection, and successful management depends on careful preoperative ...
Anil K Bhiwal +3 more
doaj +1 more source
Robot assisted laparoscopic excision of a paraganglioma: new therapeutic approach
The Paraganglioma is the most common extra-adrenal pheochromocytoma arising from neural crest (1) (It will better to write: The paraganglioma is an extra-adrenal pheocromocytoma arising from the neural crest. 10% of pheocromocytomas are extra-adrenal and
G. Cochetti +6 more
doaj +1 more source
Primary Retroperitoneal Inter-aorto-Caval Paraganglioma of the Organ of Zuckerkandl [PDF]
Tumour that arise from chromaffin cells at extra-adrenal locations are termed paragangliomas which are rare tumour. The organ of Zuckerkandl located along aortic bifurcation is the most common site of their occurrence.
Vaibhav Vikas +4 more
doaj +1 more source
Extra-adrenal paraganglioma of prostate
Extra-adrenal pheochromocytomas, or paragangliomas are rare tumors that may develop from extra-adrenal chromaffin cells, and most occur in the organ of Zuckerkandl. Extra-adrenal paraganglioma of the prostate is extremely rare. Here, we report a 53-year-old man with hypertension and lower urinary tract symptoms, who was initially diagnosed as benign ...
Hong-Hau, Wang +6 more
openaire +3 more sources
Extra adrenal retroperitoneal paraganglioma
We herein report a case of a 45-year-old Saudi lady not diabetic nor hypertensive who presented to the emergency room with a one day history of severe central and lower abdominal pain. On examination, she was hemodynamically stable and abdominal examination showed tenderness in the lower abdomen.
Hayan A, Bismar, Khalid R, Murshid
openaire +2 more sources
Non-functioning Aortocaval Paraganglioma Masquerading as Celiac Lymphnodal Metastasis
An extra-adrenal paraganglioma is a rare tumour derived from chromaffin cells of sympathetic ganglia. This report documents a rare case of a non-functional aortocaval paraganglioma in a 24-year-old woman with persistent abdominal pain.
Nikhil Gulavani +4 more
doaj +1 more source
Gangliocytic paraganglioma of the cauda equina: A rare tumor case report with literature review
Gangliocytic paragangliomas are rare, benign, encapsulated, and slow-growing tumors arising from the neuro-ectodermal ganglion or spindle cells. We describe the case of a 47-year-old male patient who presented to our department with intractable lower ...
Nigil Sadanandan Palliyil +3 more
doaj +1 more source

