Endocrinology Flashcards

1
Q

What are the differences between steroid and peptide hormones?

A

Peptide hormones are synthesised as prohormones. Steroid hormones are synthesised from cholesterol.
Peptide hormones are stored in vesicles (regulatory secretion). Steroid hormones are released immediately (constitutive secretion).
Peptide hormones bind to receptors to transduce using secondary messenger systems. Steroid hormones bind to intracellular receptors to alter gene expression.

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2
Q

Where is the pituitary gland located?

A

Superior to the sella turcica of the sphenoid bone

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3
Q

How is bitemporal hemianopia assessed?

A

Visual field perimetry

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4
Q

How are the glands in the anterior pituitary stimulated?

A

Parvocellular neurons from the hypothalamus synapse at the median eminence and release factors into the capillary plexus that pass through the portal circulation and stimulate glands

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5
Q

What factors affect somatotrophs and what hormone do they release?

A

Growth hormone releasing hormone (excitatory), somatostatin (inhibitory)
Releases growth hormone

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6
Q

What factors affect lactotrophs and what hormone do they release?

A

Dopamine (inhibitory)

Releases prolactin

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7
Q

What factors affect corticotrophs and what hormone do they release?

A

Corticotrophin releasing hormone (excitatory)

Releases adrenocorticophic hormone

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8
Q

What factors affect thyrotrophs and what hormone do they release?

A

Thyrotrophin releasing hormone (excitatory)

Releases thryoid stimulating hormone

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9
Q

What factors affect gonadotrophs and what hormone do they release?

A

Gonadotrophin releasing hormone (excitatory)

Releases FSH, LH

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10
Q

What are the effects of growth hormone?

A

Causes the production of insulin-like growth factor (IGF-1, predominantly IGF-2) in the liver which can act on body tissues to bring about growth and development.
Can act directly on body tissues as well.

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11
Q

What is a congenital cause of hypopituitarism?

A

PROP1 mutation - very rare and can be picked up early due to low GH

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12
Q

What are acquired causes of hypopituitarism?

A

Tumors, radiation, infection, trauma, surgery, apoplexy, inflammation, pre-partum infarction

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13
Q

How is pituitary function assessed?

A

Dynamic blood tests

GH and ACTH levels after insulin administration (should increase)

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14
Q

How is GH deficiency treated? How is treatment monitored?

A

GH injection

QoL questionnaires and IGF-1 levels are used as indicators

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15
Q

What is apoplexy and how does it present? What is the immediate management?

A

Intra-pitutary haemorrhage or infarction. It usually has a sudden onset and can result in bitemporal hemianopia (due to blood pooling) & diplopia/ptosis (due to cranial nerve involvement in cavernous sinus). Anti-coagulants can be used as treatment.

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16
Q

What is Sheehan’s syndrome? How does it present? How is it treated?

A

Aetiology: Lactotroph hyperplasia during pregnancy can lead to postpartum haemorrhage which causes infarction. More common in developing countries. Results in hypopituitarism.
Symptoms: lethargy, anorexia, weight loss, failure of lactation, amenorrhoea (due to deficiency in TSH, ACTH, GH, prolactin, FSH/LH)
Treatment: Focuses on replenishing depleted hormones.