Search Results 1-10 of 17102 for Phaeochromocytoma
Find out more about the symptoms, causes and treatment of this rare adrenal gland tumor, which usually is not cancer.
Subsequent biopsy of the pleural mass confirmed this to be a peripheral nerve sheath tumor. On referral to Mayo Clinic, he was asymptomatic. He denied paroxysms ...
In cortical-sparing bilateral adrenalectomy, some cortical adrenal tissue is preserved, sparing patients the dependency of exogenous steroids and potential ...
Medical Professionals news and the latest information about endocrinology.
Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.
PARPs are proteins that help repair DNA mutations. PARP inhibitors, such as olaparib, can keep PARP from working, so tumor cells can't repair themselves, and ...
A Mayo Clinic physician provides a basic framework for titrating medications before surgery for patients with pheochromocytoma and paraganglioma.
This hormone-related condition causes unusual bone and organ growth in adults. Learn about symptoms, diagnosis and treatment options.
Lynch syndrome (LS) is a hereditary cancer predisposition syndrome caused by inactivating mutations in DNA mismatch repair (MMR) genes.
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