Giantism and Acromegaly Flashcards

1
Q

What hormone is elevated in both gigantism and acromegaly?

A

Growth hormone (GH)

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2
Q

What is the key difference between gigantism and acromegaly?

A

Gigantism occurs before growth plate fusion (childhood); acromegaly occurs after growth plate fusion (adulthood).

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3
Q

What gland produces growth hormone?

A

Anterior pituitary gland

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4
Q

What hypothalamic hormone stimulates growth hormone release?

A

Growth hormone-releasing hormone (GHRH)

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5
Q

What hypothalamic hormone inhibits growth hormone release?

A

Somatostatin

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6
Q

What hormone does the liver produce in response to growth hormone?

A

Insulin-like Growth Factor 1 (IGF-1)

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7
Q

What are the typical causes of elevated GH leading to gigantism or acromegaly?

A

Pituitary adenoma, carcinoid tumors, and pancreatic islet cell tumors

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8
Q

Name one genetic condition associated with high GH levels.

A

McCune-Albright syndrome, MEN1, or Neurofibromatosis

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9
Q

What is the hallmark feature of gigantism?

A

Excessive height due to elongation of long bones

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10
Q

Name two key physical signs of acromegaly.

A

Enlarged hands/feet and coarsened facial features

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11
Q

What test is used to screen for both gigantism and acromegaly?

A

IGF-1 level (elevated in both conditions)

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12
Q

What dynamic test is used to confirm acromegaly?

A

Glucose suppression test (GH fails to suppress)

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13
Q

What imaging is used to identify pituitary adenomas?

A

MRI of the head

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14
Q

Name one medication used to treat acromegaly.

A

Octreotide (somatostatin analog) or cabergoline (dopamine agonist)

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15
Q

What is the first-line treatment for GH-secreting tumors?

A

Surgical excision of the tumor

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