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Excess pituitary hormones secretion
Inflammation or tumor of pituitary gland
Leads to chronic disease resulting from excessive production and secretion of pituitary hormones
Gigantism
Abnormal pattern of growth
Hypersecretion of growth hormone occurs before puberty
Accelerated growth of long bones
Caused by anterior pituitary adenoma
Acromegaly
Chronic metabolic condition in adults caused by hypersecretion of GH by pituitary gland
Hypersecretion of GH after puberty
Excessive overgrowth of soft tissue
Excessive jaw growth
May experience osteoarthritis
Caused by pituitary tumor or adenoma
Hypopitutarism
Caused by deficiency or absence of any pituitary hormones produced by anterior pituitary lobe
When thyrotrophin secretion is reduced, functioning of thyroid gland is affected
When corticotropin secretion is reduced, salt balance and nutrient metabolism is affected
Caused by pituitary tumor or tumor in hypothalamus
Dwarfism
Deficiency of pituitary GH in children results in short stature
Underdevelopment of body in children
Adult height of 4 foot 10 inches or less
Hyposecretion of pituitary gland hormones (GH), results in delayed growth
Can be congenital, caused by cranial tumor or hemorrhage after birth
Diabetes insipidus
Disturbance of water metabolism, resulting in extreme thirst and excessive secretion of dilute urine
Deficiency in release of vasopressin by the posterior pituitary gland
Results in excretion of copious amounts of dilute urine (polyuria)
Excessive thirst (polydipsia), fatigue, dehydration
Caused when posterior pituitary gland released reduced amounts of vasopressin
May be hereditary or insult to the hypothalamus or pituitary gland from head trauma
Simple goiter
Any enlargement of the thyroid gland usually by swelling in the neck
May be asymptomatic in early stages
Usually female
As hyperplasia (enlargement through increase in cells) increases, it presses on the esophagus
Produces difficulty swallowing
Simple goiter results from deficiency of iodine in the diet
Needed for synthesis of T3 and T4
Together known as thyroid hormone
Inadequate blood level of thyroid hormone causes anterior pituitary gland to increase secretion of thyrotropin
Keeps trying to stimulate thyroid gland to produce hormone
Continued stimulation causes thyroid gland to increase
Hashimoto thyroiditis
Chronic disease of the immune system that attacks the thyroid gland
Mostly in women
Gradual and painless lumpy enlargement of the thyroid gland
Pressure in neck and difficulty swallowing
Caused by heredity
Antibodies destroy thyroid tissue instead of stimulating it
Gland enlarges in inflammatory response
Gland tissue becomes replaced by fibrous tissue
Graves Disease
Condition of primary hyperthyroidism, occurs when entire thyroid gland hypertrophies (increase in the size of cells or tissues), results in diffuse goiter (entire thyroid gland, located at the base of your neck, swells up uniformly and smoothly)
Overproduction of thyroid hormones
Causes increased metabolism and changes
Rapid heartbeats and palpitations, nervousness, excitability, and insomnia
Weight loss
Tremor, loss of hair
Exophthalmos: outward protrusion of eyes
Thyrotoxicosis: exaggerated thyroid hormone levels
Life threatening
Caused by autoimmune response
Antibodies to thyroid antigens stimulate hyperactivity of thyroid gland
Genetics
Cretinism
Congenital hypothyroidism developing in infancy or early childhood
Thyroid gland is absent or hormone is not synthesized by thyroid gland
Causes intellectual developmental disorder and delayed growth
Child develops as a dwarf, is stocky in stature, and has a protruding abdomen
Caused by an error in fetal development
Causes thyroid gland to fail to develop
Myxedema and myxedema coma
Severe hyperthyroidism with reduced levels of T3 and T4 leads to slowing of organ function
Fatigue, muscular weakness, hair loss, weight gain
Skin is dry and scaly
Pugginess
Caused by thyroid gland inability to synthesize T4
Result of reduced amounts of thyrotrophin, radiation of thyroid gland, removal of gland
Myxedema: disease characterized by clinical manifestations associated with low metabolic rate caused by thyroid hormone deficiency
Myxedema Coma: result of severe untreated hypothyroidism exacerbated by events like MI or infection
Hyperparathyroidism
Condition caused by overactivity of one or more of the four parathyroid glands
Results in overproduction of PTH
Increase the breakdown of bone
Results in excessive calcium in blood (hypercalcemia)
Irritability of nerve and muscle tissues
Conduction defects
Caused by increased activity of parathyroid gland
Results of excessive growth (adenoma) or hyperplasia
Hypoparathyroidism
Condition in which secretion of PTH by the parathyroid glands is reduced
PTH Increases blood calcium level by stimulating bone demineralization and increasing calcium absorption in digestive tract/kidneys
When level of PTH is insufficient, calcium levels are reduced
Results in hypocalcemia
Overstimulation of skeletal muscles
Caused by surgical destruction of parathyroid gland
Accidental removal
Cushing syndrome
Condition of chronic hypersecretion of adrenal cortex, excessive cortisol levels
Fatigue, muscular weakness, weight gain, changes in appearance
Fat deposits from scapular area (buffalo humps) and in trunk
Causes protruding abdomen
Salt and water retention
Changes in mood and decreased memory
Skin becomes thin, easily bruised
Caused by hyperplasia (the increase in the number of normal-looking cells) of adrenal gland, excessive secretion of corticotrophin from pituitary gland, or tumor of cortex
Addison disease
Partial or complete failure of adrenocortical function
Manifests as fatigue, weakness, anorexia, agitation, confusion
Bronze color skin
Progressive destruction of adrenal gland and reduction in its hormones
Caused by autoimmune process, tuberculosis, hemorrhage, fungal infections, neoplasms, surgery
Diabetes mellitus
Chronic disorder of carbohydrate, fat, and protein metabolism caused by inadequate production of insulin by the pancreas or faulty use of insulin by the cells
Functional pancreas secretes insulin and maintains glucose levels within precise range
Insulin reduces blood glucose levels by transporting glucose into cells for use as energy and storage as glycogen
A reduction in insulin → hyperglycemia
Deprives cell of fuel
Cells begin to metabolize fats and proteins
Allows wastes called ketone bodies to accumulate in blood (ketosis)
Ketonuria develops as excess ketone bodies are excreted in urine
Leads to acidosis
Polyuria (abnormally large volume of urine), polyphagia (excessive hunger), polydipsia (excessive thirst), weight loss, fatigue
Caused by heredity
Type 1 Diabetes
Early onset before 30 yrs old
Little or no insulin being secreted
Difficult to control
Type 2 Diabetes
Most common
Gradual onset, older than 55 yrs
Some pancreatic function remains
Can control symptoms
Gestational diabetes
Condition of damaged ability to process carbohydrate that has onset during pregnancy
May be asymptomatic
Exhibits symptoms of diabetes mellitus
Caused by destruction of insulin by the placenta
Reduced effectiveness of maternal insulin
Fetus takes glucose from mother
Stresses balance of glucose production and usage
Elevated levels of estrogen and progesterone block insulin
Hypoglycemia
Abnormally low glucose level in the blood
occurs when excessive insulin enters the bloodstream or when the glucose release rate falls below tissue demand
sweating, nervousness, weakness, hunger, dizziness, trembling, headache, and palpitations
Extremely low blood glucose levels can cause central nervous system manifestations
Confusion, visual disturbances, behavior that may be mistaken for drunkenness, stupor, coma, and seizures
Major cause of drug-induced hypoglycemia is insulin overdose
Failure to eat a meal or excessive exercise also can trigger hypoglycemia in the insulin-dependent patient with diabetes