Endocrine - Acromegaly Flashcards

1
Q

What is the pathophysiology of acromegaly?

A

Pituitary adenoma causes unregulated growth hormone secretion

Adenoma can be microscopic or large enough to compress local structures

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2
Q

What is a rare cause of acromegaly?

A

Paraneoplastic syndrome

Cancer such as lung or pancreatic can secrete ectopic GHRH or GH

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3
Q

What symptoms can a space-occupying pituitary tumour cause?

A

Headaches
Bitemporal hemianopia

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4
Q

What does excess growth hormone lead to?

A

Frontal bossing
Coarse, sweaty skin
Macroglossia
Large nose
Large hands and feet
Prognathism (large protruding jaw)

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5
Q

What condition is strongly associated with acromegaly?

A

Carpal tunnel syndrome

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6
Q

What investigations are used for acromegaly?

A

Insulin-like growth factor-1 (IGF-1)
- Testing growth hormone directly is unreliable as it has pulsatile secretion

MRI of pituitary
- Diagnose pituitary adenoma

Growth hormone suppression test
- 75g glucose drink
- Glucose should suppress the GH level, failure indicates acromegaly

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7
Q

How is acromegaly treated?

A

Trans-sphenoidal surgery
Removes pituitary adenomas

Surgical removal of tumours

Radiotherapy as part of treatment

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8
Q

What medical options can be used for reducing growth hormone where surgery is not indicated?

A

First line
Octreotide
- Somatostatin analogue
- Blocks GH release

Second line
Pegvisomant
- GH receptor antagonist (daily subcut)

Used with other therapies
Bromocriptine
- Dopamine agonist
- Blocks GH release

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