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  2. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    Pheochromocytoma. Pheochromocytoma is a rare tumor of the adrenal medulla composed of chromaffin cells and is part of the paraganglioma (PGL) family of tumors, being defined as an intra-adrenal PGL . [2][4][5] These neuroendocrine tumors can be sympathetic, where they release catecholamines into the bloodstream which cause the most common ...

  3. Multiple endocrine neoplasia type 2 - Wikipedia

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

    Specialty. Oncology. 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 (cancer).

  4. Multiple endocrine neoplasia type 2B - Wikipedia

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

    H&E stain. Specialty. Endocrinology. Multiple endocrine neoplasia type 2B (MEN 2B) is a genetic disease that causes multiple tumors on the mouth, eyes, and endocrine glands. It is the most severe type of multiple endocrine neoplasia, [2] differentiated by the presence of benign oral and submucosal tumors in addition to endocrine malignancies.

  5. Adrenal tumor - Wikipedia

    en.wikipedia.org/wiki/Adrenal_tumor

    Oncology. An adrenal tumor or adrenal mass[2] is any benign or malignant neoplasms of the adrenal gland, several of which are notable for their tendency to overproduce endocrine hormones. Adrenal cancer is the presence of malignant adrenal tumors, and includes neuroblastoma, adrenocortical carcinoma and some adrenal pheochromocytomas.

  6. Paraganglioma - Wikipedia

    en.wikipedia.org/wiki/Paraganglioma

    Oncology. A paraganglioma is a rare neuroendocrine neoplasm that may develop at various body sites (including the head, neck, thorax and abdomen). When the same type of tumor is found in the adrenal gland, they are referred to as a pheochromocytoma. They are rare tumors, with an overall estimated incidence of 1 in 300,000. [1]

  7. Paroxysmal hypertension - Wikipedia

    en.wikipedia.org/wiki/Paroxysmal_hypertension

    Paroxysmal hypertension is episodic and volatile high blood pressure, which may be due to stress of any sort, or from a pheochromocytoma, a type of tumor involving the adrenal medulla. [citation needed] Patients with paroxysmal hypertension who test negative for pheochromocytoma are said to be suffering from a clinical entity called ...

  8. Von Hippel–Lindau disease - Wikipedia

    en.wikipedia.org/wiki/Von_Hippel–Lindau_disease

    Pheo - A pheochromocytoma is an adrenal tumor that makes and releases excess catecholamines. These tumors can cause serious health problems including stroke, heart attack, and even death. [21] Hemangioblastomas - a hemangioblastoma is a tumor that grows in the blood vessels of your brain, spinal cord or retina.

  9. Chromaffin cell - Wikipedia

    en.wikipedia.org/wiki/Chromaffin_cell

    Chromaffin cells, also called pheochromocytes (or phaeochromocytes), are neuroendocrine cells found mostly in the medulla of the adrenal glands in mammals.These cells serve a variety of functions such as serving as a response to stress, monitoring carbon dioxide and oxygen concentrations in the body, maintenance of respiration and the regulation of blood pressure. [1]