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  2. Adrenocortical adenoma - Wikipedia

    en.wikipedia.org/wiki/Adrenocortical_adenoma

    An adrenocortical adenoma or adrenal adenoma is commonly described as a benign neoplasm emerging from the cells that comprise the adrenal cortex.Like most adenomas, the adrenocortical adenoma is considered a benign tumor since the majority of them are non-functioning and asymptomatic.

  3. Adrenal gland disorder - Wikipedia

    en.wikipedia.org/wiki/Adrenal_gland_disorder

    Adrenal gland disorders (or diseases) are conditions that interfere with the normal functioning of the adrenal glands. [1] Your body produces too much or too little of one or more hormones when you have an adrenal gland dysfunction. The type of issue you have and the degree to which it affects your body's hormone levels determine the symptoms.

  4. 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.

  5. Adrenal crisis - Wikipedia

    en.wikipedia.org/wiki/Adrenal_crisis

    While studies on the prevalence of adrenal crisis in older adults are limited, one population-based study into hospital admissions for adrenal crisis found that the incidence increased with age in older individuals, going from 24.3 (60–69 years) to 35.2 (70–79 years) and 45.8 (80+ years) per million per year.

  6. Primary pigmented nodular adrenocortical disease - Wikipedia

    en.wikipedia.org/wiki/Primary_pigmented_nodular...

    PPNAD, the endocrine manifestation that comes from Carney Complex (CNC), can be syndromic or isolated. The main cause of isolated PPNAD is a mutation of PRKAR1α, located at 17q22-24, which is the gene encoding the regulatory R1α subunit of protein kinase A. Germline heterozygous PRKAR1α inactivation mutations are present in 80% of CNC patients affected by Cushing's syndrome. [8]

  7. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    Adrenal gland; the medulla (center, red) is the origin of the pheochromocytoma. There is an adrenal gland, highlighted in yellow, on top of each of the kidneys. Other clinical manifestations that have been reported include (in no particular order): [6] [13] Pallor; Heat intolerance; Weight loss; Chest and/or abdominal discomfort; Palpitations ...

  8. Adrenal insufficiency - Wikipedia

    en.wikipedia.org/wiki/Adrenal_insufficiency

    Adrenal insufficiency is a condition in which the adrenal glands do not produce adequate amounts of steroid hormones.The adrenal glands—also referred to as the adrenal cortex—normally secrete glucocorticoids (primarily cortisol), mineralocorticoids (primarily aldosterone), and androgens.

  9. Primary aldosteronism - Wikipedia

    en.wikipedia.org/wiki/Primary_aldosteronism

    [1] [10] A single adrenal gland may also be removed in cases where only one is enlarged. [4] In cases due to enlargement of both glands, treatment is typically with medications known as aldosterone antagonists such as spironolactone or eplerenone. [1] Other medications for high blood pressure and a low salt diet, e.g. DASH diet, may also be needed.