The Pituitary Gland - Clinical Cases and Discussion Flashcards

1
Q

Describe normal pituitary anatomy.

A
  • Pea-sized
  • Sits in the sella turcica of the sphenoid bone (the bottom of which is called the hypophyseal fossa)
  • Has an anterior and posterior lobe, which are separated by the pars intermedia
  • Sits directly beneath the optic chiasm
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2
Q

Describe neuroendocrine control of pituitary secretion.

A

a

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3
Q

Discuss the clinical presentation of the pituitary hyperfunction syndrome, acromegaly.

A

Soft tissue overgrowth;

  • ‘Spade like’ hands (rings)
  • wide feet (shoes)
  • Coarse facial features
  • Thick lips & tongue
  • Carpal tunnel syndrome
  • Sweating
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4
Q

Discuss the clinical presentation of the pituitary hyperfunction syndrome, Cushing’s disease.

A

High value;

  • Skin atrophy
  • Spontaneous purpura
  • Proximal myopathy
  • Osteoporosis
  • Growth arrest in children

Intermediate value;

  • Pink striae
  • Facial mooning and hirsutism
  • Oedema

Non-specific;

  • Central obesity
  • Hypertension
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5
Q

Discuss the clinical presentation of the pituitary hyperfunction syndrome, prolactinoma.

A

a

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6
Q

Discuss the biochemical diagnosis of the pituitary hyperfunction syndrome, acromegaly.

A

REPLACE THESE ANSWERS

Can GH be supressed?
Is IGF-1 elevated?
Is the rest of pituitary function normal?
Is there a pituitary tumour on MRI?
Is vision normal?
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7
Q

Discuss the biochemical diagnosis of the pituitary hyperfunction syndrome, Cushing’s disease.

A

a

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8
Q

Discuss the biochemical diagnosis of the pituitary hyperfunction syndrome, prolactinoma.

A

a

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9
Q

Describe the clinical features of hypopituitarism in adults and children.

A

a

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10
Q

Discuss the concept of neoplasms of the endocrine system as being functional (i.e. secreting hormones) and non-functional (i.e. non-secretory).

A

a

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11
Q

Discuss the concept of neoplasms being benign and malignant, in the context of the endocrine system.

A

a

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12
Q

Describe the consequences of a space-occupying lesion in the pituitary region (imaging techniques, visual field assessment).

A

a

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13
Q

Discuss the clinical management of patients with pituitary disease (pituitary surgery, radiotherapy, medical therapy and pituitary hormone replacement).

A

a

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14
Q

Discuss the complications of the pituitary hyperfunction syndrome, acromegaly.

A
  • Headache
  • Chiasmal compression
  • Diabetes mellitus
  • Hypertension
  • Cardiomyopathy
  • Sleep apnoea
  • Accelerated OA
  • Colonic polyps & CA
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15
Q

Explain the effect of excess cortisol on tissue, sodium and insulin and what diseases this could cause.

A

Excess cortisol = Cushing’s syndrome.

Tissue breakdown causes weakness of skin, muscle & bone.

Sodium retention may cause hypertension & heart failure.

Insulin antagonism may cause diabetes mellitus.

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16
Q

Name the causes of Cushing’s syndrome/disease.

A

Not all cases of Cushing’s syndrome are due to a pituitary tumour.

ACTH-dependent;

  • Pituitary tumour i.e. Cushing’s DISEASE
  • Ectopic ACTH secretion e.g. lung carcinoid

ACTH-independent;

  • Adrenal tumour e.g. adenoma or carcinoma
  • Corticosteroid therapy e.g. for asthma, IBD.
17
Q

What is the difference between Cushing’s syndrome and disease?

A

Cushing’s disease;

  • AKA secondary hypercortisolism
  • Often caused by a pituitary tumour
  • Results in production of ACTH, which stimulates excess cortisol production

Cushing’s syndrome;

  • AKA primary hypercortisolism
  • Often due to causes outside of the body e.g. corticosteroid therapy
  • Results in excess cortisol