The Pituitary Gland Clinical Case & Discussion Flashcards

1
Q

State some pituitary diseases that involve hyperfunction/hypersecretion

A
  • Acromegaly (gigantism)
  • Cushing’s disease
  • Hyperprolactinaemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

State some pituitary diseases that involve hypofunction/hyposecretion

A
  • Hypopituitarism (lower secretion of anterior pituitary hormones)
  • Cranial diabetes insipidus (lower secretion of vasopressin from the posterior pituitary gland)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What does space occupation in the pituitary region cause?

A
  • Optic chiasmal compression

(IN THE NEURO LECTURES: bilateral hemianopia)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

In terms of the clinical features of acromegaly, what symptoms/features are associated with soft tissue overgrowth?

A
  • Spade like hands
  • Wide feet (shoes)
  • Coarse facial features
  • Thick lips and tongue
  • Carpal tissue syndrome (compression of the median nerve causes numbness, weakness and tingling in the hand and arm)
  • Sweating
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the complications of acromegaly?

A

Complications:

  • Diabetes mellitus
  • Obstructive sleep apnoea
  • Hypertension
  • Headache
  • Chiasmal compression
  • Cardiomyopathy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How do we diagnose acromegaly?

A

Diagnosis of acromegaly :

  • Oral glucose tolerance test: Growth hormone (GH) fails to suppress in the presence of glucose

AND

  • ↑IGF-1
  • MRI (look for pituitary tumour)
  • Is vision normal?
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is Cushing’s syndrome?

A
  • Excess glucocorticoids/corticosteroids (i.e cortisol)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What type of hormone is cortisol and how do we know this?

A
  • CATABOLIC hormone

This is becuase it:

  • Breaks down tissue (causing weakness of skin, muscle and bone)
  • Causes sodium retention (may cause hypertension and heart failure)
  • Insulin antagonism (causing diabetes mellitus)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the symptoms and signs of Cushing’s syndome that are of high diagnostic value?

A

High value:

  • Proximal myopathy
  • Osteoporosis
  • Growth arrest in children
  • Skin atrophy
  • Spontaneous purpura
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the symptoms and signs of Cushing’s syndome that are of intermediete diagnostic value?

A

Intermediate value:

  • Pink striae
  • Oedema
  • Facial mooning and hirsutism (body hair in areas where there shouldn’t be)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the symptoms and signs of Cushing’s syndome that are of non-specific value?

A
  • Central obesity
  • Hypertension
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the ACTH dependent causes of cushing’s syndrome

A

ACTH-dependent causes (↑ACTH):

  • Pituitary tumour (which secretes ACTH)
  • Ectopic ACTH secretion (i.e small cell lung cancers and carcinoid tumours)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the ACTH independent causes of cushing’s syndrome

A

ACTH-independent causes (↓ACTH due to negative feedback):

  • Corticosteroid therapy (e.g for asthma, IBD)
  • Adrenal tumour (adenoma or carcinoma)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

State the causes of hyperprolactinaemia under the following headings:

(a) Physiological
(b) Pharamacological
(c) Pathological

A

(a) Physiological:
- Lactation
- Pregnancy
- Stress
(b) Pharmacological
- Dopamine antagonist drugs (neuroleptic e.g. chlorpromazine and anti-emetics e.g. metoclopramide) (dopamine inhibits prolactin production)
- DA-depleting agents
- Oestrogens
- Some antidepressents
(c) Pathological
- Pituitary lesions (i.e prolactinoma = excess production of prolactin from the anterior pituitary or increase in pituitary stalk pressure due to compression)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

In hyperprolactinaemia, what should we not forget to ask about?

A

Don’t forget to ask about homeopathic or herbal remedies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Whar are the clinical features of hypopituitarism in adults?

A

Clinical features in adults:

  • Tiredness (due to ↓TSH secretion)
  • Weight gain (due to ↓TSH secretion)
  • Depression (due to ↓TSH secretion)
  • Reduced libido (due to gonadotrophin deficiency)
  • Impotence (a man cannot get an erection or orgasm: due to gonadotrophin deficiency)
  • Menstrual problems (due to gonadotrophin deficiency)
  • Skin pallor (due to ↓ACTH secretion)
  • Reduced body hair (due to ↓TSH secretion and gonadotrophin deficiency)
17
Q

Whar are the clinical features of hypopituitarism in children?

A

Clinical features in children:

  • Reduced linear growth (due to ↓growth hormone secretion and TSH deficiency)
  • Delayed puberty (due to ↓ACTH secretion and gonadotrophin deficiency)
18
Q

How is cranial diabetes insipidus diagnosed?

A
  • Water deprivation test

(Explanation not in lecture: Empty the bladder then no drinks/fluids for up to 8 hours or until 3% of their body weight has been lost. Body weight, urine output, serum osmolality, urine volume, and urine osmolality are measured hourly. Normal response equates to a rise in urine osmolality to >700 mOsm/kg.)

19
Q

How is cranial diabetes insipidus treated?

A
  • DDAVP (desmopressin: This hormone which acts on the kidneys to ↓flow of urine)
20
Q

What is the differential diagnosis for cranial diabetes insipidus?

A

Differential diagnosis:

  • Post-trauma
  • Idiopathic
  • Metastatic carcinoma
  • Rare causes e.g. sarcoidosis
  • Other brain tumours e.g. germinoma
  • Craniopharyngioma
21
Q

Label the following diagram and state what it shows

A
  • Large pituitary adenoma

(REMEMBER: This causes optic chiasmal compression

22
Q

Discuss the management of pituitary tumours under the following headings:

(a) Hypersecretion
(b) Hyposecretion
(c) Tumour

A

(a) For hypersecretion:
- Dopamine (for prolactinoma)
- Somatostatin (for acromegaly)
- GH receptor antagonist (for acromegaly)
(b) For hyposecretion:
- Cortisol
- T4 (thyroxine)
- Sex steroids
- Growth hormone
- Desmopressin (hormone which acts on the kidneys to ↓flow of urine)
(c) Tumour:
- Surgery (mostly transsphenoidal: surgery done through the sphenoid sinus)
- Radiotherapy

23
Q

How is Cushing’s disease treated?

A
  • Pituitary surgery
24
Q

How is acromegaly treated?

A
  • Transsphenoidal surgery (surgery done through the sphenoid sinus to remove the pituitary tumour)
  • Somatostatin analogues (e.g. lanreotide)
  • Pegvisomant (GH antagonist)
25
Q

What are the beneficial effects of somatostatin analogues in acromegaly?

A
  • Improves soft tissue overgrowth
  • Normalises GH and IGF-1 levels in over 50% of patients
  • Induces tumour shrinkage in the majority
  • Reduced morbidity and mortality from acromegaly
26
Q

What are the adverse effects of somatostatin analogues in acromegaly?

A
  • High cost
  • Nausea, cramps, diarrhoea, flatulence (transient)
  • Cholesterol gallstones occurs in 20-30% (mostly asymptomatic
  • Slow-release preparations require monthly IM/SC injections
27
Q

How are microprolactinomas treated?

A
  • Dopamine agonists (i.e cabergoline)
28
Q

How are macroprolactinomas treated?

A

For macroprolactinomas (> 10mm):

  • Dopamine agonist (i.e cabergoline)
  • Consider transsphenoidal surgery if medical treatment fails but this is rare
29
Q

Compare and contrast the features of excess prolactin in both women and men

A

Features of excess prolactin:

WOMEN

  • Galactorrhoea (milk secretion from the breasts)
  • Amenorrhoea (absence of menstrual periods)
  • Infertility (inability to get pregnant)

MEN:

  • Galactorrhoea (milk secretion from the breasts)
  • Impotence (inability of men to get an erection)
  • Loss of libido (losing interest in sex)