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  2. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    In comparison to the specificity of elevated catecholamines in the pheochromocytoma patient, chromogranin A is a non-specific polypeptide that is high in a variety of neuroendocrine tumors. [72] However, a 2006 report from Italy found that over 90% of studied pheochromocytoma patients demonstrated elevated chromogranin A levels. [73]

  3. Multiple endocrine neoplasia type 2 - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    Multiple endocrine neoplasia type 2 (also known as "Pheochromocytoma (codons 630 and 634) and amyloid producing medullary thyroid carcinoma", [1] "PTC syndrome," [1] and "Sipple syndrome" [1]) is a group of medical disorders associated with tumors of the endocrine system.

  4. Multiple endocrine neoplasia type 2B - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    Without thyroidectomy, almost all patients with MEN2B develop medullary thyroid cancer, in a more aggressive form than MEN 2A. [13] [19] The ideal age for surgery is 4 years old or younger, since cancer may metastasize before age 10. [14] Pheochromocytoma - a hormone secreting tumor of the adrenal glands - is also present in 50% of cases. [14]

  5. Multiple endocrine neoplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine_neoplasia

    In 1974 Sizemore et al. showed that the MEN 2 category included two groups of patients with MTC and pheochromocytoma: one with parathyroid disease and a normal appearance (MEN 2A) and the other without parathyroid disease but with mucosal neuromas and mesodermal abnormalities (MEN 2B).

  6. Adrenal tumor - Wikipedia

    en.wikipedia.org/wiki/Adrenal_tumor

    Pheochromocytoma is a neoplasm composed of cells similar to the chromaffin cells of the mature adrenal medulla. Pheochromocytomas occur in patients of all ages, and may be sporadic, or associated with a hereditary cancer syndrome, such as multiple endocrine neoplasia (MEN) types IIA and IIB, neurofibromatosis type I, or von Hippel–Lindau ...

  7. Pacak–Zhuang syndrome - Wikipedia

    en.wikipedia.org/wiki/Pacak–Zhuang_syndrome

    Mutations in the genes encoding alpha subunits of hypoxia-inducible factors (HIF-alpha) have not previously been identified in any cancer. [4]In the Pacak–Zhuang syndrome, patients have somatic gain of function mutations in the genes encoding for HIF2A, leading to prolonged HIF-2α activity and, thus, an increase in its half-life. [5]

  8. Taylor Swift's Spicy Red Mini Reveals a Sexy 'T ... - AOL

    www.aol.com/lifestyle/taylor-swifts-spicy-red...

    The star hit the red carpet at L.A.'s Crypto Arena in a black-and-white look and moody glam that many thought was Reputation-coded, when in fact it was littered with easter eggs for her latest ...

  9. Phenoxybenzamine - Wikipedia

    en.wikipedia.org/wiki/Phenoxybenzamine

    Its only current clinical use is in preparing patients with pheochromocytoma for surgery; its irreversible antagonism and the resultant depression in the maximum of the agonist dose-response curve are desirable in a situation where surgical manipulation of the tumour may release a large bolus of pressor amine into the circulation. Typically ...