Pituitary Disease Flashcards
What are some types of pituitary disease?
Tumours:
Adenoma,
Prolactinoma
Acromegaly
Cushing’s disease
Deficiencies:
Hypopituitarism
Growth hormone deficiency
Gonadotrophin deficiency
SIADH
Describe features of a pituitary adenoma
Most common pituitary tumour. It is benign and non secretory so just presents with a headache and visual field defects (bitemporal hemianopia)
Diagnosis - MRI brain
Treatment - Neurosurgery which is usually trans-sphenoidal. Or radiotherapy
What is the most common secretory tumour of the pituitary?
How is it classified
Prolactinoma.
Microadenoma if <10mm.
Macroadenoma if >10mm
Explain the presentation of a prolactinoma
High levels of prolactin which can cause oligomenorrhoea/amenorrhoea, galactorrhoea, infertility and vaginal dryness in women. In men it can cause erectile dysfunction and reduced facial hair.
In both sexes you get headaches and visual field defects.
What are the investigations for a prolactinoma?
MRI brain and serum prolactin
What is the management of a prolactinoma
Pharmacological - Dopamine agonists (Carbergoline/bromocriptine) which decreases serum prolactin
Hormone replacement with oestrogen if galactorrhoea and fertility are not an issue
Surgical - Trans-sphenoidal resection
Radiotherapy
What is the cause of Acromegaly?
Caused by excessive GH production from anterior pituitary.
The hypothalamus secretes GH releasing hormone every few hours and can increase with low blood glucose levels, lack of food, increased exercise and increased sleep.
Negative feedback to hypothalamus by GH and somatostatin.
What are the effects of growth hormone?
Increased release of glucose into blood
Muscle growth
Thickened bone
Insulin resistance
What is the presentation of Acromegaly in adults?
Insidious onset
Hyperhydriasis
Headaches
Lethargy
Joint pains
Facial changes: coarsening of features, frontal bossing, enlarged nose, prognathism (protrusion/extension of mandible), macroglossia
Deepening of voice,
Enlarged hands and feet
Obstructive sleep apnoea
Diabetes mellitus
CHF (heart failure)
GI cancer
Carpal tunnel syndrome
What does excess growth hormone in children cause?
Increased growth velocity = gigantism
What are the investigations for acromegaly?
Serum Insulin growth factor 1 (first line)
Oral glucose tolerance test (failure to suppress GH in response to glucose
MRI brain
What is the treatment for acromegaly?
surgery/radiation if pituitary adenoma
Medications such as somatostatin analogues which limit GH production
What are the causes of SIADH?
Strokes
Haemorrhages
Trauma
Drugs (mood stabilisers or anti epileptics)
Surgery
Pulmonary diseases (Infections, pneumothorax, asthma, cystic fibrosis)
Ectopic ADH release from tumours (small cell carcinoma)
Infections
Family history
What are the symptoms of SIADH?
These are caused by hyponatraemia:
Headaches
Nausea
Vomiting
Muscle cramps
Tremors
Cerebral oedema - Confusion, mood swings, hallucinations
Why do you get hyponatraemia in SIADH?
ADH increases the water reabsorption (dilutes sodium) and this increases BP which reduces aldosterone which causes sodium excretion.