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Trial results show belzutifan shrinks rare neuroendocrine tumors and improves symptoms in patients
A multicenter Phase II clinical trial led by researchers at The University of Texas MD Anderson Cancer Center demonstrated ...
A new study published in The New England Journal of Medicine reported that the HIF-2α inhibitor belzutifan has shown ...
Pheochromocytoma is a rare tumor that develops in the adrenal glands. It affects the production of adrenalin and can result in high blood pressure and other health issues. Pheochromocytoma is usually ...
Pheochromocytoma is a rare tumor of the adrenal medulla that secretes substances called catecholamines. The adrenal glands are a pair of small glands sitting on the top of the kidneys. An adrenal ...
Pheochromocytoma is a catecholamine-producing tumor that originates from chromaffin cells of the adrenergic system, most commonly in the adrenal medulla. There are two main steps in the diagnosis of ...
Pheochromocytomas are neural crest-derived tumors that produce catecholamines, such as epinephrine and norepinephrine, and arise mainly from the adrenal gland. Closely affiliated tumors of ...
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New Drug for Rare Neuroendocrine Tumors Shows Durable Activity
BERLIN -- Belzutifan (Welireg) induced durable responses in advanced pheochromocytoma or paraganglioma (PPGL) in a single-arm ...
a person’s age, as pheochromocytoma tend to grow faster in people under 50 the size of the mass, with larger masses growing more quickly According to a 2022 study, masses less than 1 centimeter (cm) ...
Please provide your email address to receive an email when new articles are posted on . The patient is a 65-year-old white man with a past medical history significant for severe coronary artery ...
Adults with pheochromocytoma or paraganglioma are nearly five times more likely to experience a vertebral fracture, a hallmark of osteoporosis, when compared with adults with nonfunctional adrenal ...
The First International Symposium on Pheochromocytoma, held in October 2005, included discussions about developments concerning these rare catecholamine-producing tumors. Recommendations were made ...
Pheochromocytoma fascinates and, at times, confounds clinicians. The symptoms due to hypersecretion of catecholamines can mimic more than 30 medical disorders. 1 This rare tumor can be lethal if left ...
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