Endocrine System Diseases
Introduction to Human Diseases:
Chapter 14
Endocrine System Terminology
• Endocrine
• Exocrine
• Hormone
• Target organ
• Hypersecretion
• Hyposecretion
Pituitary Gland Diseases
• Hyperpituitarism
– Hypersecretion of growth hormone (GH) by the
pituitary
• Gigantism
– GH hypersecretion during puberty and growth years
• Person is very tall, proportioned normally
• Acromegaly
– GH hypersecretion during adulthood
– Disfiguring overgrowth of bones & soft tissues
Hyperpituitarism
• Other aspects:
– Gigantism:
• Fairly abrupt onset
• Non-life threatening
• Growth up to 6 inches/yr
– Agromegaly:
• Gradual onset
• Decreases life expectancy
• Headache, sinus problems, skin changes, paresthesias, joint
pain, visual disorders
Hypopituitarism
• Deficiency of any or all of the pituitary
hormones
• Usually involve GH and gonadotropin
– LH, FSH, Prolactin, Oxytocin
• Less commonly involved:
– ACTH and TSH
• Panhypopituitarism:
– All hormones are deficient
Hypopituitarism
• S/S: varies with hormone deficiency and
age of disease onset
– In childhood: S/S are dwarfism and delayed
development of 2ndary sexual characteristics
– In adults: S/S are amenorrhea, infertility,
lowering of testosterone levels, libidy, hair
loss.
– ACTH & TSH deficiency: general S/S:
fatigue, pallor, anorexia, poor stress response
Hypopituitarism:
• Treatment: hormone replacement
Diabetes Insipidus
• Hyposecretion of vasopressin
– ADH (antidiuretic hormone)
• S/S: extreme polyuria, thirst, very dilute
urine produced, leads to dehydration
• Etiology: anything that destroys the
pituitary or idiopathic
• Treatment: fluid replacement, hormone
replacement (tablet, nasal spray)
Thyroid Gland Diseases
• Goiter
– Enlargement or hyperplasia of thyroid gland
• Simple goiter
– Goiter not caused by infection, tumor, other
hypo- or hyperthyroid condition
– More common in females
– Sporadic and endemic types
Goiter
• Sporadic type
– Ingestion of certain foods, drugs (goitrogens)
• Endemic type
– Diet deficiency of iodine
• Etiology: hyperplasia due to inability to
make sufficient T3 and T4, compensation
• Treatment: T3 or T4 or iodine
replacements, surgery, dietary changes
Thyroiditis
• Inflammation of thyroid gland
• Females more than males
• Etiology & types:
– Autoimmune
• Antibodies to thyroid hormones
• Myxedema, Grave’s disease
• Hashimoto’s thyroiditis (lymphocytes infiltrate)
– Subacute granulomatous
• Follows an infection (mumps, influence, adenovirus)
– Miscellaneous
• Bacterial infections (TB, syphilis, suppurative)
Thyroiditis
• S/S: may have no symptoms or thyroid
enlargement, pain and dysphagia
• Autoimmune thyroiditis = most common
type, common in females
• Treatment varies with type:
– Hormone replacement, steroid, antibiotics,
anti-inflammatories, pain meds
Grave’s Disease
• Hyperthyroidism
– Grave’s disease is most common hyperthyroid disease
• Hypersecretion of T3 and T4
• May cause thyrotoxicosis
– Diffuse effect, multiple symptoms
• Females mostly, 30-40 YOA
• Etiology:
– Genetic or immunologic
Grave’s Disease
• S/S:
• Thyrotoxicosis
– Anxiety, insomnia, heat intolerance, sweating, muscle
wasting, weight loss, tachycardia, hypertension
– Thyroid storm: critical episode of thyrotoxicosis
• Ophthalmopathy: exophthalmos (protrusion of
eyeballs, “frightened” appearance)
• Dermopathy: thickened skin on legs/feet
(“orange skin”
• Exacerbations & remissions
Grave’s Disease
• Treatment:
– Varies with disease severity & patient age
– Antithyroid drugs, surgery, radioactive iodine
therapy
Hypothyroidism
• Hyposecretion of thyroid hormones
• More common in women, esp. over 40
YOA
• Two versions:
– Cretinism
• Congenital form
– Myxedema
• Starts in childhood or adulthood
Hypothyroidism
• Etiology:
– Dietary, metabolic, iatrogenic, congenital,
inflammatory, chronic autoimmune
• S/S:
– Children: growth retardation, delayed sexual
development, impaired intelligence
– Adults: cold intolerance, fatigue, constipation, weight
gain, anorexia, dry skin, brittle hair &nails,
cardiomegaly, myxedema coma
• Treatment: Hormone replacement meds
Parathyroid Diseases
• Hyperparathyroidism
• Affects women more than men (2:1)
• Excessive secretion of PTH by gland
causes abnormalities of calcium (Ca++)
and phosphates (PO4--)
• Effects:
– Hypercalcemia (most important effect)
– hypophosphatemia
Hyperparathyroidism/
Hypercalcemia
• Primary disease: parathyroid adenoma
• Secondary disease: chronic RF, calcium deficient
diet, calcium malabsorption
– Any condition that tends to reduce circulating levels
of calcium
• S/S: many patients are asymptomatic
– Brittle bones, arthralgias, calcium renal stones,
polyuria, nausea, vomiting, fatigue, muscle weakness
or atrophy, cardiac arrythmias
Hyperparathyroidism
• Treatment:
– Surgical removal of gland(s)
– Increasing fluid & sodium intake
– Meds that increase calcium excretion
– Treatment varies with the etiology, primary or
secondary
Hypoparathyroidism
• Undersecretion of PTH by gland
– Hypocalcemia
– Excessive calcium deposition into bones
• Etiology: iatrogenic (surgical) or inherited
• S/S: paresthesias of extremities, muscle
cramps (tetany), depresion, irritability,
laryngospasm, seizures, brittle nails, hair
loss
Hypoparathyroidism
• Treatment:
– Vitamin D and calcium supplements
– Periodic lab tests to determine serum levels
– High calcium, low phosphorus diet
Adrenal Disease
• Cushing’s Syndrome:
– Hypersecretion of hormones by the adrenal
cortex
– Cortisol excess
– More common in women
– May be due to:
• Oversecretion of ACTH
• Benign or malignant neoplasm of adrenal cortex
• Iatrogenic (prolonged steriod treatment)
Cushing’s Disease
• S/S:
– “moon facies”, truncal obesity with thin limbs,
“buffalo hump”, decreased glucose tolerance,
muscle weakness, hypertension, anxiety,
depression
• Treatment:
– Surgery for tumor removal, drug or radiation
to decrease ACTH secretion
Other Adrenal Diseases
• Addison’s Disease
– Hyposecretion of adrenal cortex hormones
– Decreased ability to handle physiological stress
– Low BP, increased temperature
• Pheochromocytoma
– Tumor of adrenal medulla
– Secretes catecholamines
• Epinephrine
• Norepinephrine
• Like SNS, increases blood pressure, heart rate, skin flushing
Diabetes Mellitus
• Chronic carbohydrate metabolism disorder
due to insulin deficiency or inadequate
insulin utilization by cells
• Insulin
– Pancreatic endocrine secretion (hormone)
– Made by islet of Langerhans
– Lowers serum glucose level
– Allows cellular uptake and use of glucose
Diabetes Mellitus (DM)
• Disorder characterized by:
– Hyperglycemia
– Ketosis (ketones in the blood)
– Acidosis (excess hydrogen ions in the blood)
– Ketoacidosis
Diabetes Mellitus
• Types of DM:
– Type 1 (juvenile onset)
• Immune-mediated absence of insulin
• Often seems to appear abruptly & emergently
– Type 2 (adult onset)
• Able to make insulin
• Often obesity related
– Gestational (GDM)
• Occurs during pregnancy & resolves after delivery
• 25% risk of DM development later in life
• Tend to have large babies (over 9 lbs)
Diabetes:
• Etiology:
– Autoimmune, genetic, pancreatic disorders,
drugs, tumors, Cushing’s, cells become
insensitive to insulin in some
• S/S:
– Three P’s: polyuria, polydipsia, polyphagia
– Increased susceptibility to infections &
vascular diseases, retinopathy, renal failure
Diabetes:
• Treatment:
– Type 1: insulin administration
– Type 2: diet & exercise
• Oral hypoglycemics
• insulin
Diabetic Emergencies:
• Insulin shock (severe hypoglycemia)
• Diabetic Ketoacidosis
– Severe hyperglycemia & ketoacidosis
– Altered mental status, possible coma
– Severe dehydration

Endocrine system diseases

  • 1.
    Endocrine System Diseases Introductionto Human Diseases: Chapter 14
  • 2.
    Endocrine System Terminology •Endocrine • Exocrine • Hormone • Target organ • Hypersecretion • Hyposecretion
  • 3.
    Pituitary Gland Diseases •Hyperpituitarism – Hypersecretion of growth hormone (GH) by the pituitary • Gigantism – GH hypersecretion during puberty and growth years • Person is very tall, proportioned normally • Acromegaly – GH hypersecretion during adulthood – Disfiguring overgrowth of bones & soft tissues
  • 4.
    Hyperpituitarism • Other aspects: –Gigantism: • Fairly abrupt onset • Non-life threatening • Growth up to 6 inches/yr – Agromegaly: • Gradual onset • Decreases life expectancy • Headache, sinus problems, skin changes, paresthesias, joint pain, visual disorders
  • 5.
    Hypopituitarism • Deficiency ofany or all of the pituitary hormones • Usually involve GH and gonadotropin – LH, FSH, Prolactin, Oxytocin • Less commonly involved: – ACTH and TSH • Panhypopituitarism: – All hormones are deficient
  • 6.
    Hypopituitarism • S/S: varieswith hormone deficiency and age of disease onset – In childhood: S/S are dwarfism and delayed development of 2ndary sexual characteristics – In adults: S/S are amenorrhea, infertility, lowering of testosterone levels, libidy, hair loss. – ACTH & TSH deficiency: general S/S: fatigue, pallor, anorexia, poor stress response
  • 7.
  • 8.
    Diabetes Insipidus • Hyposecretionof vasopressin – ADH (antidiuretic hormone) • S/S: extreme polyuria, thirst, very dilute urine produced, leads to dehydration • Etiology: anything that destroys the pituitary or idiopathic • Treatment: fluid replacement, hormone replacement (tablet, nasal spray)
  • 9.
    Thyroid Gland Diseases •Goiter – Enlargement or hyperplasia of thyroid gland • Simple goiter – Goiter not caused by infection, tumor, other hypo- or hyperthyroid condition – More common in females – Sporadic and endemic types
  • 10.
    Goiter • Sporadic type –Ingestion of certain foods, drugs (goitrogens) • Endemic type – Diet deficiency of iodine • Etiology: hyperplasia due to inability to make sufficient T3 and T4, compensation • Treatment: T3 or T4 or iodine replacements, surgery, dietary changes
  • 11.
    Thyroiditis • Inflammation ofthyroid gland • Females more than males • Etiology & types: – Autoimmune • Antibodies to thyroid hormones • Myxedema, Grave’s disease • Hashimoto’s thyroiditis (lymphocytes infiltrate) – Subacute granulomatous • Follows an infection (mumps, influence, adenovirus) – Miscellaneous • Bacterial infections (TB, syphilis, suppurative)
  • 12.
    Thyroiditis • S/S: mayhave no symptoms or thyroid enlargement, pain and dysphagia • Autoimmune thyroiditis = most common type, common in females • Treatment varies with type: – Hormone replacement, steroid, antibiotics, anti-inflammatories, pain meds
  • 13.
    Grave’s Disease • Hyperthyroidism –Grave’s disease is most common hyperthyroid disease • Hypersecretion of T3 and T4 • May cause thyrotoxicosis – Diffuse effect, multiple symptoms • Females mostly, 30-40 YOA • Etiology: – Genetic or immunologic
  • 14.
    Grave’s Disease • S/S: •Thyrotoxicosis – Anxiety, insomnia, heat intolerance, sweating, muscle wasting, weight loss, tachycardia, hypertension – Thyroid storm: critical episode of thyrotoxicosis • Ophthalmopathy: exophthalmos (protrusion of eyeballs, “frightened” appearance) • Dermopathy: thickened skin on legs/feet (“orange skin” • Exacerbations & remissions
  • 15.
    Grave’s Disease • Treatment: –Varies with disease severity & patient age – Antithyroid drugs, surgery, radioactive iodine therapy
  • 16.
    Hypothyroidism • Hyposecretion ofthyroid hormones • More common in women, esp. over 40 YOA • Two versions: – Cretinism • Congenital form – Myxedema • Starts in childhood or adulthood
  • 17.
    Hypothyroidism • Etiology: – Dietary,metabolic, iatrogenic, congenital, inflammatory, chronic autoimmune • S/S: – Children: growth retardation, delayed sexual development, impaired intelligence – Adults: cold intolerance, fatigue, constipation, weight gain, anorexia, dry skin, brittle hair &nails, cardiomegaly, myxedema coma • Treatment: Hormone replacement meds
  • 18.
    Parathyroid Diseases • Hyperparathyroidism •Affects women more than men (2:1) • Excessive secretion of PTH by gland causes abnormalities of calcium (Ca++) and phosphates (PO4--) • Effects: – Hypercalcemia (most important effect) – hypophosphatemia
  • 19.
    Hyperparathyroidism/ Hypercalcemia • Primary disease:parathyroid adenoma • Secondary disease: chronic RF, calcium deficient diet, calcium malabsorption – Any condition that tends to reduce circulating levels of calcium • S/S: many patients are asymptomatic – Brittle bones, arthralgias, calcium renal stones, polyuria, nausea, vomiting, fatigue, muscle weakness or atrophy, cardiac arrythmias
  • 20.
    Hyperparathyroidism • Treatment: – Surgicalremoval of gland(s) – Increasing fluid & sodium intake – Meds that increase calcium excretion – Treatment varies with the etiology, primary or secondary
  • 21.
    Hypoparathyroidism • Undersecretion ofPTH by gland – Hypocalcemia – Excessive calcium deposition into bones • Etiology: iatrogenic (surgical) or inherited • S/S: paresthesias of extremities, muscle cramps (tetany), depresion, irritability, laryngospasm, seizures, brittle nails, hair loss
  • 22.
    Hypoparathyroidism • Treatment: – VitaminD and calcium supplements – Periodic lab tests to determine serum levels – High calcium, low phosphorus diet
  • 23.
    Adrenal Disease • Cushing’sSyndrome: – Hypersecretion of hormones by the adrenal cortex – Cortisol excess – More common in women – May be due to: • Oversecretion of ACTH • Benign or malignant neoplasm of adrenal cortex • Iatrogenic (prolonged steriod treatment)
  • 24.
    Cushing’s Disease • S/S: –“moon facies”, truncal obesity with thin limbs, “buffalo hump”, decreased glucose tolerance, muscle weakness, hypertension, anxiety, depression • Treatment: – Surgery for tumor removal, drug or radiation to decrease ACTH secretion
  • 25.
    Other Adrenal Diseases •Addison’s Disease – Hyposecretion of adrenal cortex hormones – Decreased ability to handle physiological stress – Low BP, increased temperature • Pheochromocytoma – Tumor of adrenal medulla – Secretes catecholamines • Epinephrine • Norepinephrine • Like SNS, increases blood pressure, heart rate, skin flushing
  • 26.
    Diabetes Mellitus • Chroniccarbohydrate metabolism disorder due to insulin deficiency or inadequate insulin utilization by cells • Insulin – Pancreatic endocrine secretion (hormone) – Made by islet of Langerhans – Lowers serum glucose level – Allows cellular uptake and use of glucose
  • 27.
    Diabetes Mellitus (DM) •Disorder characterized by: – Hyperglycemia – Ketosis (ketones in the blood) – Acidosis (excess hydrogen ions in the blood) – Ketoacidosis
  • 28.
    Diabetes Mellitus • Typesof DM: – Type 1 (juvenile onset) • Immune-mediated absence of insulin • Often seems to appear abruptly & emergently – Type 2 (adult onset) • Able to make insulin • Often obesity related – Gestational (GDM) • Occurs during pregnancy & resolves after delivery • 25% risk of DM development later in life • Tend to have large babies (over 9 lbs)
  • 29.
    Diabetes: • Etiology: – Autoimmune,genetic, pancreatic disorders, drugs, tumors, Cushing’s, cells become insensitive to insulin in some • S/S: – Three P’s: polyuria, polydipsia, polyphagia – Increased susceptibility to infections & vascular diseases, retinopathy, renal failure
  • 30.
    Diabetes: • Treatment: – Type1: insulin administration – Type 2: diet & exercise • Oral hypoglycemics • insulin
  • 31.
    Diabetic Emergencies: • Insulinshock (severe hypoglycemia) • Diabetic Ketoacidosis – Severe hyperglycemia & ketoacidosis – Altered mental status, possible coma – Severe dehydration