Acromegaly and Prolactinoma Flashcards
Define acromegaly
abnormal growth of hands, feet and face due to overproduction of GH
Name the co-morbidities of acromegaly
- Hypertension and heart disease
- Cerebrovascular events and headache
- Arthritis
- Sleep apnea
- Insulin – resistant diabetes
What is the diagnosis of acromegaly dependent on?
- Clinical Features
- GH
- IGF-I
What are the presenting features of acromegaly?
- Acral (hands + feet) enlargement
- Arthralgias (joint stiffness)
- Maxillofacial changes
- Excessive sweating
- Headache
- Hypogonadal symptoms
In the criteria for diagnosing acromegaly, what result shows no acromegaly?
random GH <0.4 ng/ml and normal IGF-I
When would you do a glucose tolerance test (GTT) in diagnosing acromegaly?
If either GH>0.4 ng/ml or high IGF-I
How much glucose is given in a GTT?
75g
What result would exclude acromegaly after a GTT?
IGF-I normal and GTT nadir GH <1 ng/ml
What are the objectives of therapy in acromegaly?
- restoration of basal GH and IGF-I to normal levels
- relief of symptoms
- reversal of visual and soft tissue changes
- prevention of further skeletal deformity
- normalization of pituitary function
What are some options for acromegaly treatment?
- Pituitary surgery
- Medical therapy
- Radiotherapy
What is the primary treatment for all types of pituitary adenoma (except prolactinoma)?
Transsphenoidal pituitary surgery
What makes transsphenoidal pituitary surgery harder?
- Large size
- Invasiveness
What are 2 important determinants of success of surgery?
- size of tumour
- the surgeon
What are some examples of medical therapy?
- Dopamine agonists e.g. cabergoline
- Somatostatin analogues
- Growth Hormomne receptor antagonist
What are problems with radiotherapy?
- Loss of pituitary function in the long-term
- Potential damage to local structures – e.g. eye nerves
- Control of tumour growth / excess hormone secretion not always achieved
- Life-long monitoring needed for all patients