Endocrine Disorders
3 Major Types of Endocrine Conditions
Hormone excess
-Tumor, autoimmune, genetic mutation
Hormone resistance- Usually genetic (lack of hormone receptor or ability to respond)
Hormone deficiency
-Gland destruction (autoimmune, infection, tomor)
Diagnosis of Endocrine Disorders
Endocrine Dysfunction
Hyperfunction - Excessive amount of hormone
Three levels of dysfunction
Hypofunction - Inadequate amount of hormone
Primary- Endocrine gland itself
Secondary- Abnormal pituitary activity
Tertiary- Dysfunction of hypothalamic origin
Causes
Neoplasia- Hypofunction or hyperfunction of gland itself or any endocrine tissue the gland affects
Endocrine-disrupting compounds (EDC)- Chemical in environment that can alter endogenous hormone functions
Autoimmune - Antibodies target endocrine gland, may cause hypofunction or hyperfunction
Suppression/stimulation tests
CT scan/MRI
Urinary collection over 24 hours
Urinary hormone levels assessed in some instances
Ultrasound
Immunoassays or blood levels of hormones most important
Treatments of Endocrine Disorders
Hormone replacement therapy
-Glucocorticoids, thyroid hormones, sex steroids, ADH
Suppression of hormone overproduction
-Medications, surgery, radiation
Hypopituitarism
One or more of the pituitary hormones
Panhypopituitarism
- Complete loss of all pituitary hormones
- Rare
Causes
Trauma, ischemia, and infarction can cause sudden loss of pituitary function (Sheehan’s syndrome)
Primary adenoma
- Most common cause
- Benign neoplasm
- With growth can compress pituitary gland in sella turcica (Interfere with pituitary function)
Pituitary tumor, brain surgery, radiation of brain tumor, congenital disorder
Craniopharyngioma
- Benign neoplasm close to pituitary gland or pituitary stalk
Pituitary apoplexy
- Sudden destruction of the pituitary tissue due to infarction or hemorrhage into gland
- Traumatic brain injury most common cause
Sheehan’s Syndrome
- Ischemia or infarction of the pituitary after childbirth because of severe hemorrhage
- Degree of necrosis correlates with hemorrhage
- Develop deficiency of ACTH, TSH, FSH, LH, ADH, and PRL
Diabetes Insipidus (DI)
Lack of ADH or response to ADH
Dilute, large volume urine
Posterior pituitary hypopituitarism
Categories of disease
Central DI- Lack ADH from the posterior pituitary
Nephrogenic DI- Kidney fails to respond to ADH
click to edit
Hyperpituitarism
Pituitary adenoma
- Most common cause
- May produce ACTH, TSH, or GH
- Prolactinoma most common form: secretes PRL
Large tumors may cause headaches and visual disturbances (because of proximity to optic nerves)
Goiter
May or may not present with thyroid dysfunction signs and symptoms
May develop with:
-Excess TSH
-Low iodine levels
-Goitrogens
Enlargement of the thyroid