Pituitary DO Flashcards
HPA Axis hormones functions
- respond to stress
- thyroid stim, growth, reproduction
Which pituitary gland is the producer? which is the storer?
Anterior - Producer
Posterior - Storer
Anterior and Posterior Pituitary glands secrete which hormones?
Growth hormone excess is referred to as _____
Growth hormone deficiency is referred to as _____
what stim and inhibits Growth hormone secretion?
GHRH stim
Somatostatin inhibits
High levels of growth hormone are usually caused by ____
a GH-secreting tumor
what increases growth hormone secretion?
think big picture
What decreases growth hormone secretion?
Giantism vs Acromegaly
Which occurs during childhood?
Giantism = during childhood (b4 growth plates close)
Acromegaly = Adulthood
genetic causes of Giantism
- familial isolated pituitary adenoma
multiple endocrine neoplasia type 1 (MEN1) - McCune-Albright syndrome (MAS)
- Carney complex with onset during
- prepubescence
Giantism SS
- Longitudinal acceleration of linear growth secondary to insulinlike growth factor I (IGF-I) excess
- Tumor mass may cause headaches, visual changes due to optic nerve compression, and hypopituitarism
- Hyperprolactinemia is a common finding; it results from pituitary growth hormone (GH) excess,
Acromegaly WU
- Two baseline GH levels are obtained prior to ingestion of 75 or 100 g of oral glucose, and additional GH measurements are made at 30, 60, 90, and 120 minutes following the oral glucose load. A rise, or no suppression is diagnostic.
- Measure serum GH 1 hour after oral administration of 100 g of glucose. Clearly elevated GH levels (>10 ng/mL) after oral glucose, combined with the clinical picture, secure the diagnosis of acromegaly, while a normal GH level (< 5 ng/mL) after oral glucose essentially excludes the diagnosis.
GnRH can be measured
IGF-I can be measured
Prolactin is often also measured since it can be co-secreted in 20% of tumors
Imaging: MRI of brain
CT scans of abdomen/pelvis or chest if brain is negative
Acromegaly Complications
Acromegaly Trmnt
- # 1 Trnassphenoidal Sx
- Radiation
- Octreotide -
- Bromocriptine -
- Pegvisomant (Somavert) -
MC pituitary hormone deficiency in children
Growth Hormone Deficiency
2 main ways you get pituitary dwarfism
- Isolated LOW growth hormone
- Generalized - ALL pituitary hormones are LOW
Pituitary Dwarfism WU
- IGF-1 levels
- XR of LT Hand to determine bone age
- MRI to r/o calcifications, tumors, structural anomalies
- ACTH, 8 am serum cortisol level, LH, FSH, Prolactin levels
Dx Criteria for Pituitary Dwarfism
Dwarfism Trmnt
- recombinant Growth Hormone
- +/- other pituitary hormone replacement
Which HPA hormones should be eval for deficiencies?
ALL
Cortisol
Thyroid
ADH
Sex hormone around time of puberty
Why do new moms need to try breastfeeding ASAP
Stim Prolactin -> breastfeeding
What stim prolactin secretion
- sleep
- stress
- pregnancy
- chest wall stimulation or trauma
- TRH, dopamine receptor antagonists, primary hypothyroidism
- prolactinomas (tumor)