Tidbits 2 Flashcards
If someone has acromegaly they almost certainly have____.
A pituitary macroadenoma.
Pituitary stalk disruption would likely cause hyper or hypoprolactinemia?
Hyperprolactinemia, due to loss of tonic inhibition by dopamine
What is the most common functional pituitary adenoma?
Prolactinoma. 10:1 F:M. Tends to be a microadenoma in a woman of reproductive age (mean 34)
Men get macroadenomas and rarely lactate. More often mass effect symptoms.
Cortisol excess is caused by ACTH dependent and independent mechanisms. Name several of each
ACTH dependent (75%) Corticotroph Adenoma (Cushing’s Disease) Ectopic Cushing’s (ACTH/CRH tumors)
ACTH independent (25%)
Adrenal Adenomas
Adrenal Carcinoma
Nodular Hyperplasia (micro or macro)
Cortisol levels fluctuate. When are they low and high?
Low - midnight
Highest - am
Fatigue/weakness Anorexia, nausea/vomiting and weight loss Generalized malaise/aches Scant Axillary/Pubic hair Hyponatremia and Hypoglycemia
What is likely the cause?
Central adrenal insufficiency.
Primary adrenal insufficiency most common cause?
CRF, ACTH, Cortisol, Aldosterone, androgen levels?
Addison. (Also TB, HIV, fungi, etc)
CRF, ACTH are up.
Cortisol, aldosterone, androgens are down.
What is meant by “Autoimmune Polyglandular Syndromes”?
If a person has one autoimmune disorder, they are likely to have another in the same category. Two syndromes exist, APS-1, and APS-2
What diseases are associated with APS-1? What gene is implicated?
Adrenal Insufficiency (Addison’s Disease)
Hypoparathyroidism
Type 1 Diabetes Mellitus
Mucocutaneous Candidiasis
Autoimmune Regulator Gene is implicated
What diseases are associated with APS-2? What gene is implicated?
Adrenal Insufficiency (Addison’s Disease)
Hypothyroidism (Hashimoto’s Thyroiditis)
Type 1 Diabetes Mellitus
HLA Associated
Two main causes of primary aldosteronism?
Aldosterone producing adenoma (unilateral) Idiopathic hyperaldosteronism (66%) - bilateral adrenal hyperplasia
What familial syndromes are associated with pheochromocytoma (the 10%)?
Multiple Endocrine Neoplasia Type 2A/2B
Von Hippel Lindau Syndrome
Neurofibromatosis Type 1
Familial Paragangliomas (SDH Mutations)
What is the rule of 10 regarding pheochromocytoma?
10% bilateral
10% familial
10% benign
10% ectopic (outside adrenal gland)
**Triad of HTN plus sweating, headaches, palpitations raises suspicion for pheochromocytoma
Hyperpigmentation =
Addisons = Adrenal insufficiency