Growth Hormone Problems Flashcards

(31 cards)

1
Q

What is the main cause of Gh Hypersecretion

A

Tumours

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2
Q

What is gigantism

A

A rare condition that causes abnormal growth in children

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3
Q

What parameter is most obviously increased in children with gigantism

A

Height (but girth also affected)

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4
Q

What causes gigantism

A

Pituitary tumours

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5
Q

What are rarer causes of gigantism

A

Mccune-Albright syndrome
Carney Complex
Multiple endocrine neoplasia (MEN1)
Neurofibromatosis

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6
Q

What is Mccune-Albright syndrome

A

Causes abnormal growth in bone tissue, patces of brown skin and gland abnormalities

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7
Q

What is Carney complex

A

An inheritied condition that causes non-cancerious tumours on connective tissue, cancerours or non cancerous endocrine tumours and spots on darker skin

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8
Q

What is MEN1

A

inherited disorder causing tumours of pituitary gland, pancreas or parathyroid gland

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9
Q

What is neurofibromatosis

A

An inherited disorder that causes tumours in the nervous system

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10
Q

What are symptoms of gigantism

A
very large hands and feet
thick toes and fingers
Prominent jaw and forehead
Coarse facial features
excessive sweating
Insomnia 
Delayed puberty
irregular menstrual periods
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11
Q

How do you make the diagnosis of gigantism

A

Bloods (GH and IGF-1)

Oral glucose tolerance test

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12
Q

Why do a glucose tolerance test in gigantism

A

In acromegaly failure of suppression occurs, and there may be a paradoxical rise in GH in response to the glucose challenge.

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13
Q

What is treatment of gigantism

A

Surgical resection (transphenoidal)

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14
Q

What is acromegaly

A

The clinical manifestation of excessive growth hormone after epiphyeal plates have sealed. Long bones cant increase in height but they grow in other directions

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15
Q

What is the characteristic feature of acromegaly

A

Large hands and feet

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16
Q

What are the causes of acromegaly

A

Pituitary adenoma

Ectopic release of GHRH from a tumour elsewhere (bronchial carcinoid)

17
Q

What are symptoms of acromegaly (x9)

A
Big features but same height 
Arthritis 
Organ dysfunction 
Headaches (if tumour) 
Bi-temporal heminaopea (if tumour)
Carpal tunnel syndrome
Lower voice pitch 
Macroglossia 
Sweating
18
Q

What effects of organ dysfunction can be seen in acromegaly

A

Hypertrophic heart
Hypertension
Type-2 Diabetes
Colorectal cancer

19
Q

What is treatment for acromegaly

A

Trans-sphenoidal surgery
Somatostatin analogues
Dopamine agonists
GH antagonists

20
Q

Name a somatostatin analogue

21
Q

What do somatostatin analogues do?

A

They block GH release

22
Q

Name a dopamine agonist

A

Bromocriptine

23
Q

What do dopamine agonsit do

A

Block GH relase

24
Q

Name a GH antagonist

25
What can cause hyposecretion of GH
A deficiency in GHRH A deficiency in GH release from pituitary Genetic mutations or underexpression of GH receptor Precocious puberty Hypothyroid dwarfism
26
What is precocious puberty?
Excess GnRH stimulates puberty early causing kids to have stunted growth
27
What are features of hypothyroid dwarfism
Children retain infantile features with stunted growth doe to loos of permissive effects of TH on GH.
28
What is the screening test for Acromegaly
IGF-1 levels
29
What is the diagnostic test for acromegaly
Oral glucose tolerance load test
30
What investigations should you do for someone with suspected acromegaly
``` Test IGF-1 levels Oral glucose tolerance load test Bloods (Glu, Calcium, Phosphate) Radiology Visual field exam ECHO/ECG ```
31
Why would you do an ECHO/ECG in acromegaly investigations
To assess for cardiovascular risk factors