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  2. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    Pheochromocytoma is a rare tumor of the adrenal medulla composed of chromaffin cells ... [non-primary source needed] Kidney failure is brought about by catecholamine ...

  3. Von Hippel–Lindau disease - Wikipedia

    en.wikipedia.org/wiki/Von_Hippel–Lindau_disease

    In individuals with a family history of VHL disease, one hemangioblastoma, pheochromocytoma or renal cell carcinoma may be sufficient to make a diagnosis. As all the tumours associated with VHL disease can be found sporadically, at least two tumours must be identified to diagnose VHL disease in a person without a family history.

  4. Von Hippel–Lindau tumor suppressor - Wikipedia

    en.wikipedia.org/wiki/Von_Hippel–Lindau_tumor...

    Nonsense or deletion mutations of VHL protein have been linked to type 1 VHL with a low risk of pheochromocytoma (adrenal gland tumors). Type 2 VHL has been linked to missense mutations and is linked to a high risk of pheochromocytoma. Type 2 has also been further subdivided based on risks of renal cell carcinoma.

  5. Adrenal tumor - Wikipedia

    en.wikipedia.org/wiki/Adrenal_tumor

    The adrenal cortex is composed of three distinct layers of endocrine cells which produce critical steroid hormones.These include the glucocorticoids, which are critical for regulation of blood sugar and the immune system, as well as response to physiological stress; the mineralcorticoid aldosterone, which regulates blood pressure and kidney function; and certain sex hormones.

  6. Adrenal gland disorder - Wikipedia

    en.wikipedia.org/wiki/Adrenal_gland_disorder

    Pheochromocytoma originates from chromaffin cells and is a kind of neuroendocrine tumor. ... and renal renin production and secretion are all potential causes of the ...

  7. Organ of Zuckerkandl - Wikipedia

    en.wikipedia.org/wiki/Organ_of_Zuckerkandl

    The organ of Zuckerkandl is of pathological significance in the adult as a common extra-adrenal site of pheochromocytoma though the most common extra-adrenal site is in the superior para-aortic region between the diaphragm and lower renal poles. [9] Extra-adrenal tumors account for around 25% of all cases of pheochromocytoma. [10]

  8. Using Minoxidil for Hair Loss? Know About These ... - AOL

    www.aol.com/using-minoxidil-hair-loss-know...

    An adrenal gland tumor known as pheochromocytoma. Kidney failure or another condition that requires dialysis. A recent history of heart attack. Low blood pressure.

  9. 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. The tumors may be benign or malignant .