Acromegaly
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Introduction
Incidence of 3-4 cases/million each year.
The Case of...
a simple case introducing clincial presentation and calling for a differential diagnosis to get students thinking.
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Causes and Risk Factors
Pituitary adenomas are behind 95% of cases of acromegaly. Other causes include:
- hypothalamic tumours such as gliomas, hamartomas
- ectopic pituitary remnamts
- paraneoplastic effects of adenocarcinomas such as breast
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Pathophysiology
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Signs and Symptoms
History
- coarse features and deep voice
- headaches
- fatigue
- sweating
- sleep apnea
- decreased libido
- impotence
- menstrual problems
- visual impairment
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Investigations
- lab investigations
- diagnostic imaging
Lab Investigations
Suppression test can be used.
Random GH, if low, can exclude acromegaly, but is not useful as a routine test.
IGF-1 and IGFBP-3 can also be useful.
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Differential Diagnosis
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Treatments
surgery
radiotherapy
somatostatin analogues
DA agonists
GH receptor antagonists
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Consequences and Course
Cardiovascular disease accounts for over half of acromegaly deaths.
Conditions that can also occur include:
- acral growth
- carpal tunnel syndrome
- diabetes mellitus, impaired glucose tolerance
- arthritis
- congestive heart failure
- hypertension
- goitre and organomegaly
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Resources and References
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Topic Development
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