Prepared by Prof. Zeinab Al-Wahsh for Spring 2024-2025 Lectures 2-3
Endocrine glands release hormones (chemical messengers) into the bloodstream to various organs and tissues.
Example: Pancreas secretes insulin; Thyroid gland regulates chemical activity levels via pituitary instructions.
Size: About the size of a pea (1.27 cm in diameter).
Often called the master gland.
Located on the inferior aspect of the brain, with anterior and posterior lobes.
Controlled by the hypothalamus.
Occurrence: About 6 in every 100,000 adults.
Cause: Abnormal growth hormone (GH) production after normal growth.
Typically caused by a benign tumor in the pituitary gland.
Risk factors: Prior history of a pituitary tumor.
Elevated secretion of anterior pituitary hormones leading to excessive GH.
Causes include:
Pituitary or hypothalamus malfunction.
Primary adenoma of hormone-secreting cells.
Lack of feedback from target gland.
Two types:
Acromegaly: occurs in adulthood.
Gigantism: occurs in childhood with extreme height.
Symptoms include:
Enlarged hands and feet.
Visual problems, headaches.
Oily skin, hyperglycemia, jaw protrusion, joint pain.
Menstrual disturbances, impotence.
May include:
Hypo-pituitarism, high blood pressure, glucose intolerance, diabetes.
Cardiovascular disease, carpal tunnel syndrome, sleep apnea, arthritis.
Other complications include uterine fibroids and vision abnormalities.
High levels of growth hormone and IGF-1.
Spine x-ray shows abnormal bone growth.
MRI or CT might reveal pituitary tumors.
Provide emotional support and encourage expression of feelings.
Frequent skin care and interventions for joint pain.
Prepare client for radiation therapy or hypophysectomy if needed.
No hormones from anterior pituitary lobes due to various causes (tumors, surgery, etc.).
Leads to atrophy of several organs including heart, kidneys, and adrenal glands.
Symptoms include impotence, extreme weight loss, hypometabolism, amenorrhea.
Treatment involves hormone replacement therapy (HRT).
Overview: Water metabolism issue due to ADH deficiency.
Classification includes primary neurogenic, secondary neurogenic, nephrogenic, and drug-related.
Symptoms of DI:
Polyuria (excessive urination), polydipsia (excessive thirst).
Dehydration, dry skin, headache.
Condition involves hypo-secretion of adrenal cortex hormones, commonly due to autoimmune destruction.
Symptoms include weakness, GI disturbances, bronze pigmentation, electrolyte imbalances (hyperkalemia).
Treatment involves monitoring vital signs, maintaining fluid/electrolyte balance, and educating on lifelong corticosteroid use.
Caused by increased ACTH from tumors.
Symptoms: central obesity, hypertension, moon face, and muscle weakness.
Treatment may involve adrenalectomy and the need for lifelong steroid supplementation post-surgery.
Myxedema: severe hypothyroid state often caused by Hashimoto's thyroiditis.
Symptoms: lethargy, cold intolerance, weight gain, dry skin.
Diagnosis includes T4 test, high TSH in primary cases, and thyroid function tests.
Caused by hyper-secretion of thyroid hormone leading to increased metabolism.
Symptoms include exophthalmos, increased appetite, nervousness.
Diagnosis includes decreased TSH and elevated T3/T4 levels.
Treatment may involve medication, radioactive iodine, or surgery.
Caused by decreased parathyroid hormone, typically after thyroid surgery.
Symptoms: hypocalcemia, tingling, cramps, tetany.
Caused by increased parathyroid hormone.
Symptoms: bone deformities, fractures, elevated calcium levels.
Management includes monitoring electrolytes and potential surgical intervention.