Hypopituitarism is a medical term describing deficiency (hypo) of one or more hormones of the pituitary gland. The pituitary produces a number of important regulating hormonal factors, and its function is mainly regulated by the hypothalamus. In endocrinology, deficiency of multiple hormones of the anterior lobe is generally referred to as hypopituitarism, while deficiency of the posterior lobe generally only leads to diabetes insipidus. If both lobes malfunction, the term panhypopituitarism (generalised hypopituitarism) is used.

Contents

1 Physiology 2 Causes 3 Diagnosis 4 Replacement therapy 5 See also 6 External links

Physiology

Primary hormones of the anterior pituitary include

• growth hormone (GH) - growth and glucose homeostasis
• luteinizing hormone (LH) - menstrual cycle and reproduction
• follicle stimulating hormone (FSH) - same
• adrenocorticotropic hormone (ACTH) - stimulates glucocorticoid production in the adrenal gland
• thyroid stimulating hormone (TSH) - stimulates thyroxine production in the thyroid
• prolactin (PRL) - stimulates milk production in the breast

The posterior pituitary produces antidiuretic hormone (ADH) and oxytocin, the former regulating plasma osmolarity and the latter regulating uterine contractions during childbirth.

Growth hormone is often the first hormone lost, so most people with hypopituitarism lack GH as well as one or more others. As for the posterior pituitary, ADH deficiency is the main problem, while oxytocin deficiency rarely causes clinically significant problems.

Causes

Hypopituitarism and panhypopituitarism can be congenital or acquired. A partial list of causes and forms:

• Congenital hypopituitarism
  • Hypoplasia of the pituitary
    • Isolated idiopathic congenital hypopituitarism
    • Associated with other congenital syndromes and birth defects
      • Septo-optic dysplasia
      • Holoprosencephaly
      • Chromosome 22 deletion syndrome
      • Rapaport syndrome
  • Single gene defect forms of anterior pituitary hormone deficiency
• Acquired hypopituitarism
  • trauma (e.g., skull base fracture)
  • surgery (e.g., removal of pituitary neoplasm)
  • tumor (secretory and non-secretory pituitary or hypothalamic neoplasms)
  • inflammation (e.g. sarcoidosis or autoimmune hypohysitis)
  • radiation (e.g., after cranial irradiation for childhood leukemia)
  • shock
    • (Sheehan's syndrome is hypopituitarism after heavy bleeding in childbirth)
  • hemochromatosis
• other diseases.

Diagnosis

Hypopituitarism may come to medical attention by symptoms or features of pituitary hormone deficiency (e.g., poor growth, hypoglycemia, micropenis, delayed puberty, polyuria, impaired libido, fatigue, and many others), or because the physician has diagnosed one of the many disorders and conditions associated with hypopituitarism listed above and tests for it.

Replacement therapy

Hypopituitarism and panhypopituitarism are treated by replacement of appropriate hormones.

• GH is replaced with growth hormone.
• TSH is replaced with thyroxine.
• ACTH is usually replaced with hydrocortisone but any glucocorticoid may be used.
• LH and FSH are most often replaced by supplying the appropriate sex steroids (e.g., testosterone or estrogen and progestin), but can occasionally be given by continuous subcutaneous infusion (pump) to induce fertility.
• Prolactin is not usually replaced.
• ADH is replaced most commonly with oral or nasal desmopressin.
• Oxytocin is most important during labor and delivery at the end of pregnancy, and can be replaced in that circumstance by pitressin.

See also

• growth hormone deficiency
• pituitary gland

External links

• All about Hypopituitarism (http://www.hypopituitarism.info/)