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Hyperpituitarism is a condition due to the primary hypersecretion of pituitary hormones; [3] [medical citation needed] it typically results from a pituitary adenoma.In children with hyperpituitarism, disruption of growth regulation is rare, either because of hormone hypersecretion or because of manifestations caused by local compression of the adenoma.
The symptoms of Cushing's disease are similar to those seen in other causes of Cushing's syndrome. [5] Patients with Cushing's disease usually present with one or more signs and symptoms secondary to the presence of excess cortisol or ACTH. [6] Although uncommon, some patients with Cushing's disease have large pituitary tumors (macroadenomas).
The symptoms depend on what part of the pituitary is affected. Lymphocytic adenohypophysitis (LAH) occurs when the anterior pituitary cells are affected by autoimmune inflammation resulting in either no symptoms, adrenal insufficiency (if the ACTH producing cells are affected), hypothyroidism (if the TSH producing cells are damaged), or ...
Hormone secreting pituitary adenomas cause one of several forms of hyperpituitarism.The specifics depend on the type of hormone. Some tumors secrete more than one hormone, the most common combination [8] being GH and prolactin, which present as Gigantism or Acromegaly and unexpected lactation (in both men and women).
Hypophysitis, inflammation of the pituitary gland.; Autoimmune hypophysitis (or lymphocytic hypophysitis), inflammation of the pituitary gland due to autoimmunity.; Nelson's syndrome, may occur after surgical removal of both adrenal glands, an out-dated method of treating Cushing's disease.
Hyperpituitarism, the increased (hyper) secretion of one or more of the hormones normally produced by the pituitary gland; Hypopituitarism, the decreased (hypo) secretion of one or more of the hormones normally produced by the pituitary gland; Panhypopituitarism a decreased secretion of most of the pituitary hormones; Pituitary tumours
Adrenocorticotropic hormone deficiency is characterized by nonspecific symptoms such as fatigue, anorexia, unintentional weight loss, and hypoglycemia. Pale skin may contribute to patients' diminished appearance and aid in differentiating between primary and secondary adrenal insufficiency.
The initial symptoms of pituitary apoplexy are related to the increased pressure in and around the pituitary gland. The most common symptom, in over 95% of cases, is a sudden-onset headache located behind the eyes or around the temples. It is often associated with nausea and vomiting.