Acromegaly Flashcards
Acromegaly
Clinical manifestation of excessive growth hormone
Most common cause
Unregulated GH secretion by pituitary adenoma
Presentation SOL
Headaches
Bitemporal hemianopia
Presentation due to overgrowth of tissues
Prominent forehead and brow
Large nose
Large tongue
Large hands and feet
Large protruding jaw
Arthritis from imbalanced growth of joints
Organ dysfunction caused by GH
Hypertrophic heart
HTN
T2DM
Colorectal cancer
Investigations
Raised insulin-like growth factor 1
OGTT (normally GH is suppressed with hyperglycaemia)
MRI brain for pituitary tumour
First line treatment
Trans-sphenoidal surgery
Treatment if inoperable or surgery unsuccessful
Somatostatin analogue
Pegvisomant
Dopamine agonists
Somatostatin analogue
Directly inhibits release of GH
Octreotide
Pegvisomant
GH receptor antagonist
Once daily SC administration
Doesn’t reduce tumour volume so surgery still needed if mass effect
Dopamine agonists
Bromocriptine
Effective only in minority of patients