Professional Documents
Culture Documents
Diseases of The Pituitary Gland
Diseases of The Pituitary Gland
Diseases of The Pituitary Gland
Dr Junaid Shaik
Diagnostics IB
Anatomy of the pituitary
gland
Pea-sized, oval gland
Suspended by the pituitary stalk (infundibulum)
Rests on the sella turcica
Divided into an anterior and posterior lobe
The anterior lobe is derived from an out pouching of the roof
of the pharynx
Posterior lobe is an extension of the hypothalamus
Release is controlled Prolactin Also called Also called FSH is released LH is released in Blood osmolarity is Stimulates
by the hypothalamus releasing thyrotropin corticotropin in response to response to constantly uterine
through GHRH and hormone by gonadotropin- gonadotropin- monitored by contraction
GHIH hypothalamus Released by the The release of releasing releasing osmoreceptors— and dilatation
results in anterior pituitary ACTH is hormone hormone (GnRH) specialized cells of the cervix
Anabolic function of release of in response to regulated by the (GnRH) by the by the within the
protein synthesis prolactin thyrotropin corticotropin- hypothalamus hypothalamus hypothalamus that It is released
releasing releasing are particularly continuously
Stimulates liver to Promotes hormone (TRH) by hormone (CRH) FSH stimulates Responsible for sensitive to the throughout
break down lactation in the hypothalamus from the the production ovulation and concentration of childbirth
glycogen to glucose women after hypothalamus and production of sodium ions and
pregnancy Triggers the maturation of oestrogen and other solutes. It is also
Stimulates adipose release of thyroid Stimulates the sex cells, or progesterone in responsible for
cells to break down In non- hormones by the adrenal glands gametes, women and ADH is also known the “milk-
stored fat pregnant thyroid gland to secrete including ova stimulates as vasopressin ejection reflex”
women cortisol in women and testosterone in after childbirth
prolactin sperm in men men In response to high when the child
secretion is blood osmolarity begins to
inhibited by ADH is released suckle
prolactin- and the target
inhibiting MSH cells are those of May assist in
hormone (PIH Stimulates melanin production in skin in response to the renal tubules, promoting
which is UV light exposure causing water maternal-child
actually MSH with oestrogen = darker skin pigmentation during reabsorption bonding
dopamine) pregnancy especially around the areolas and labia
Hypopituitarism
Causes: Clinically (those of deficient hormones):
Compression of the
gland by an FSH & LH: amenorrhoea, oligomenorrhoea, infertility, loss of libido, loss of
adenoma or Ca sexual function, osteoporosis
Infection e.g. GH: decrease in muscle mass, central obesity, growth retardation
meningitis, ACTH: leads to adrenal insufficiency, failure to thrive, delayed puberty,
encephalitis features similar to Addison’s disease
Sheehan’s syndrome TSH: features of hypothyroidism
Brain injury Prolactin: inability to breastfeed
Congenital ADH: features of diabetes insipidus
hypoplasia Oxytocin: probably stunted social development
Investigations: Management:
Blood tests for the respective hormones Correct hormonal imbalance
(Note: basal levels, when samples were Addressing the underlying
taken (e.g. morning) cause
Addressing the clinical
If any stimulation
presentation
No direct way to measure ADH
Pituitary adenoma
Causes: Clinically:
Tumours of the pituitary
gland (most are benign) GH: Increased bone growth
Most are Prolactin: Unexpected lactation (in men and women)
macroadenomas (> Compression of the optic nerve at the optic chiasma: bitemporal
10mm) hemianopia
Headache
Features of raised intracranial pressure (RIP)
Investigations:
Blood tests (hormones)
CT or MRI of the head
Treatment:
Medical and/or surgical
intervention depending
on the type of tumour
Hyperprolactinaemia
Causes: Clinically:
Compression of the pituitary
stalk (e.g. craniopharyngioma) Amenorrhoea
Prolactinoma Menorrhagia
Drugs that block the effects of Galactorrhoea in non-pregnant women and in men
dopamine at the pituitary stalk In men: features of hypogonadism
(e.g. phenothiazines) Headache
(Dopamine supresses prolactin
secretion) Treatment:
No treatment in
Excess prolactin inhibits mild cases
secretion GnRH which inhibits Dopamine
FSH and LH = decreased sex agonist (e.g.
hormone production cabergoline and
(hypogonadism) bromocriptine)
Occasionally
Investigations: radiotherapy or
Blood test (prolactin) (elevated)
surgery
MRI (tumour)
Acromegaly and gigantism
Causes: Clinically:
Gigantism: Severe headaches
Excess growth and Large hands, feet, nose, lips, ears
height before closure Thick skin
of the epiphyseal Deep voice
plates Frontal bossing
Prognathism
Acromegaly: Macroglossia
Excess growth Increased sweating
following closure of Spinal stenosis
the epiphyseal Cranial nerve palsies
plates Carpal tunnel syndrome
Most common cause
is a pituitary
adenoma Investigations:
GH suppression test following oral
Treatment: glucose intake
Surgery MRI
Radiotherapy
Medical intervention
Craniopharyngioma
Cause: Treatment:
Tumour of the pituitary Surgery
gland derived from Radiotherapy
embryonic tissue
Clinically:
Bitemporal hemianopia
Headache
Excessive sleepiness
Diabetes insipidus
(resistance to ADH)
Polydipsia
Stunted growth (GH
insufficiency)
Fatigue and low BP (low
ACTH)
Diabetes insipidus
Cause: Clinically: