Malignant neoplasm of medulla of right adrenal gland is a rare type of cancer that affects the medulla or the inner part of the adrenal gland. This type of cancer is also known as pheochromocytoma, which is a type of neuroendocrine tumor that develops from the chromaffin cells in the adrenal gland. Pheochromocytoma is a rare tumor, accounting for less than 0.2% of all cancers.
The adrenal gland is a small gland located above the kidney that produces hormones that regulate the body's metabolism, blood pressure, and response to stress. The adrenal gland has two parts: the outer layer called the cortex and the inner layer called the medulla. The medulla is responsible for producing hormones such as adrenaline and noradrenaline, which are involved in the body's response to stress.
Malignant neoplasm of medulla of right adrenal gland occurs when the chromaffin cells in the medulla start growing uncontrollably and form a tumor. This tumor can produce high levels of hormones, leading to symptoms such as high blood pressure, sweating, and rapid heartbeat. In some cases, the tumor may not produce any symptoms, and it may be detected incidentally during a routine medical examination.
The exact cause of malignant neoplasm of medulla of right adrenal gland is unknown. However, some genetic mutations have been associated with the development of this type of cancer. These mutations can be inherited or acquired during a person's lifetime. Some of the inherited genetic mutations that can increase the risk of developing this type of cancer include multiple endocrine neoplasia type 2 (MEN 2) and von Hippel-Lindau (VHL) syndrome.
If you experience any of the symptoms associated with malignant neoplasm of
Malignant Neoplasm of the Medulla of the Right Adrenal Gland is a rare form of cancer that occurs in the adrenal gland located above the kidney. The adrenal gland is responsible for producing hormones that regulate blood pressure, sugar levels, and the body's response to stress. Treatment options for this ty...
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