Acromegaly/Gigantism Flashcards

1
Q

What percentage of pituitary tumors are GH-producing tumors?

A

10%.

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2
Q

What hormone is produced in approximately 40% of somatotroph adenomas?

A

PRL.

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3
Q

What are common symptoms of hyperprolactinemia?

A
  • Amenorrhea
  • Galactorrhea.
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4
Q

What are mammosomatotroph adenomas?

A

A subset of tumors that produce both GH and PRL.

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5
Q

What clinical condition do GH-producing tumors cause in adults?

A

Acromegaly.

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6
Q

What clinical condition do GH-producing tumors cause in children?

A

Gigantism.

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7
Q

What are the most striking features of acromegaly?

A
  • Enlargement of the lower jaw (prognathism)
  • Changes in nose and lips
  • Frontal bossing.
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8
Q

What oral cavity changes are associated with acromegaly?

A
  • Malocclusion
  • Increased spacing between teeth
  • Enlargement of the tongue.
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9
Q

What causes a hollow, resonant voice in acromegaly patients?

A

Changes in the vocal cords and soft tissues of the hypopharynx.

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10
Q

What is a common respiratory issue in patients with acromegaly?

A

Sleep apnea.

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11
Q

What percentage of patients with acromegaly experience arthritis?

A

75%.

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12
Q

What is the prevalence of carpal tunnel syndrome in acromegaly patients?

A

50%.

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13
Q

What cardiovascular issues are associated with acromegaly?

A
  • Increased prevalence of hypertension (25 to 35%)
  • Diabetes mellitus (10 to 25%).
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14
Q

Why are random GH level measurements not useful for diagnosing acromegaly?

A

GH is secreted in a pulsatile manner and normal levels can be large (>50 ng/mL).

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15
Q

What is the most reliable test for diagnosing acromegaly?

A

Glucose tolerance test.

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16
Q

What do IGF-I levels indicate in the context of acromegaly?

A

An integrated index of GH production.

17
Q

What imaging study is preferred for evaluating tumor growth after acromegaly diagnosis?

18
Q

What are the goals of therapy in acromegaly?

A
  • Reverse or prevent tumor mass effects
  • Reduce long-term morbidity and mortality from excess GH.
19
Q

What percentage of patients with microadenomas achieve GH levels lower than 2.5 ng/mL after transsphenoidal surgery?

A

Approximately 80%.

20
Q

Name a medical therapy for acromegaly.

A
  • Dopamine agonists (e.g., cabergoline)
  • Somatostatin analogues (e.g., octreotide, lanreotide)
  • GH receptor antagonist (e.g., pegvisomant).
21
Q

Is radiation recommended as primary therapy for acromegaly?

22
Q

What are the risks associated with radiation therapy for acromegaly?

A
  • Long time (5 to 10 years) for GH level reductions
  • High incidence of hypopituitarism and other complications.