Pituitary Flashcards
symptoms Acromegaly
proximal muscle weakness and joint pain, tongue enlargement, deepened voice, thick and leathery skin, acne, visual changes caused by pressure on the optic nerve, and headaches.
Affected individuals have a reduced life expectancy. They are prone to cardiovascular disease, diabetes mellitus, and colorectal cancer.
adrenocorticotropic hormone (ACTH) level is increased
Cushing’s disease results.
thyroid-stimulating hormone (TSH) level is excessive
hyperthyroidism develops.
Hypopituitarism symptoms
Headaches Visual changes (decreased visual acuity or decreased peripheral vision) Loss of sense of smell Nausea and vomiting Seizures
SIADH causes
The most common cause is cancer, especially small cell lung cancer. Although SIADH tends to be self-limiting when caused by head trauma or drugs, it is chronic when associated with tumors or metabolic diseases.
- Syndrome of inappropriate antidiuretic hormone (SIADH)
SIADH symptoms
Fluid retention Serum hypoosmolality Dilutional hyponatremia Concentrated urine in the presence of normal or increased intravascular volume Low urine output Increased body weight
Diabetes insipidus symptoms
Excretion of large quantities of urine (2-20 L/day)
A very low specific gravity (<1.005)
Urine osmolality of <100 mOsm/kg (100 mmol/kg)
Identification of central DI can be made with
the water deprivation test.
Before the test, body weight and urine osmolality, volume, and specific gravity are measured. Sometimes serum osmolality is also measured.
The patient is deprived of water for 8 to 12 hours and then given desmopressin acetate (1-deamino-8-D-arginine vasopressin [DDAVP]) subcutaneously or nasally.
Urine and potentially serum are then periodically measured for response to the DDAVP.
Treatments for Patients with Diabetes Insipidus
Care of a patient with DI also includes maintaining adequate hydration and patient education for long-term management. A therapeutic goal is maintenance of fluid and electrolyte balances.
Treatment for hypopituitarism
The treatment for hypopituitarism often consists of surgery or radiation therapy followed by lifelong hormone therapy. Appropriate hormone therapy is used to correct the deficiency (e.g., GH, corticosteroids, TSH, sex hormones).
Treatment of SIADH
Treatment of SIADH is directed at the underlying cause. Medications that stimulate ADH release should be avoided or discontinued.