A4- Pituitary Gland Flashcards

1
Q

Hormones in the anterior lobe and posterior lobe?

A

Anterior lobe:1. Prolactin

  1. ACTH
  2. TSH
  3. GH
  4. LH
  5. FSH

Posterior lobe:

  1. Vasopressin
  2. Oxytocin
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2
Q
A
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3
Q

Classification of pituitary adenomas by pathology is

A
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4
Q

Examples of pituitary tumours?

A
  • Pituitary adenoma
  • Craniopharyngioma
  • Meningioma
  • Hypothalamic astrocytoma/glioma
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5
Q

Pituiatry adenoma

Presenting symptoms due to

A
  1. Hormonal dysfunction
    • Underproduction (hypopituitarism)
    • Hormonal hypersecretion
  2. Local tumour growth and pressure effect
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6
Q

Hypopituitarism

What deficiencies does it include?

A
  • GH deficiency
  • Gonadotrophin deficiency: loss of libido, loss of secondary sexual characteristics, menstrual dysfunction, ED
  • ACTH deficiency: hypocortisolism
  • TSH deficiency: secondary hypothyroidism
  • Vasopressin deficiency: diabetes insipidus
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7
Q

Ix for pituitary

Basal hormone measurement?

A
  • Prolactin
  • TSH, fT3 and fT4.
  • Cortisol, ACTH
  • LH, FSH, tesosterone or oetsradiol
  • IGF1
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8
Q

Ix for pituitary

Dynamic hormone measurement

A
  • TRH stimulation
  • GnRH stimulation
  • Glucagon test
  • Dexamethasone suppression test
  • Oral glucose tolerance test with GH measurement
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9
Q

Cushing’s syndrome symptoms/presentation?

A

• Moon facies
• Facial plethora
• Supraclavicular fat
pads
• Buffalo hump
• Truncal obesity
• Weight gain
• Purple striae
•Proximal muscle weakness
•Easy bruising
•Hirsutism
•Hypertension
•Osteopenia
•Diabetes mellitus/IGT
• Impaired immune
function/poor wound healing

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10
Q

Cushing’s syndrome vs. Cushing’s disease

A

• Cushing’s syndrome is a syndrome due to excess cortisol
from pituitary, adrenal or other sources (exogenous
glucocorticoids, ectopic ACTH, etc.)

• Cushing’s disease is hypercortisolism due to excess
pituitary secretion of ACTH (about 70% of cases of
endogenous Cushing’s syndrome)

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11
Q

Medical management of pituitary tumours

A

Which pharmacologic option to choose depends on
type of tumor:
• Dopamine agonists: bromocriptine, cabergoline- most
useful for prolactinomas, less useful for GH secreting
adenomas
• Somatostatin analog (Octreotide, Octreotide LAR)-most useful for acromegaly
• Pegvisomant (GH receptor blocker)- useful in
acromegaly refractory to somatostatin analogues
• Other: ketoconazole, metyrapone, mitotane- for
Cushing’s disease- use limited by side effects, expense and lack
of efficacy

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12
Q

Indications for intervention pituitary tumours

A
  • Tumour growth on imaging
  • Hormonal hypersecretion
  • Visual field defects
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13
Q

Pituitary surgery options?

A

Transphenoidal approach:
used for 95% of pituitary tumors

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14
Q

Indications for Surgery for Pituitary tumours

A
  • Surgery is the first-line treatment of symptomatic pituitary adenomas.
  • Useful when medical or radiotherapy fails
  • Surgery provides prompt relief from excess hormone secretion and mass effect.
  • Indicated in pituitary apoplexy with compressive symptoms
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15
Q

Complications of Transsphenoidal
Surgery

A
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16
Q

Pituitary tumours

Indications for radiotherapy

A
  • Incomplete resection of tumours
  • Progressive disease after surgery
  • Recurrent tumours
17
Q

Pituitary tumours

Genetic predisposition?

A
  • MEN type 1 syndrome
  • Familial isolated pituitary adenoma (FIPA)
18
Q

Most common • Enteropancreatic tumours?

A

Gastrinoma 40%

19
Q

Most common Anterior pituitary tumours

A

Prolactinoma

20
Q

What is Pituitary apoplexy

A

Apoplexy means bleeding into an organ or loss of blood flow to an organ. Pituitary apoplexy is commonly caused by bleeding inside a noncancerous (benign) tumor of the pituitary. These tumors are very common and are often not diagnosed. The pituitary is damaged when the tumor suddenly enlarges.

21
Q
A