The document discusses various disorders related to endocrine glands, focusing on the pituitary, thyroid, parathyroid, adrenal glands, and pancreatic islets. Key conditions include hypersecretion and hyposecretion of hormones leading to issues like gigantism, acromegaly, hyperthyroidism, and diabetes mellitus. It also outlines symptoms, causes, and treatment options for these disorders.

1. Disorders of
Endocrine Glands
Mr. Mayur Gaikar
Assistant Professor
Department of Pharmacology
College of Pharmacy (For Women), Chincholi, Nashik.

2. Disorders of the pituitary gland
Hypersecretion of anterior pituitary hormones
Gigantism & acromegaly:
The most common cause is prolonged hypersecretion of
growth hormone (GH), usually by a hormone secreting pituitary
tumour. The conditions are only occasionally due to excess growth
hormone releasing hormone (GHRH) secreted by the hypothalamus.

3. Hyposecretion of other pituitary hormones of both the
anterior & posterior lobes damage to the optic nerves, causing
visual disturbances.
The effects of excess GH include:
•Excessive growth of bones.
•Enlargement of internal organs.
•Formation of excess connective tissue enlargement of the
heart & raised blood pressure reduced glucose tolerance & a
predisposition to diabetes mellitus.

4. Gigantism
This occurs in children when there is excess GH while
epiphyseal cartilages of long bones are still growing, i.e.
before ossification of bones is complete. It is evident mainly
in the bones of the limbs, & affected individuals may grow to
heights of 2.1 to 2.4 m, although body proportions remain
normal

5. Historical artwork showing effects of normal & abnormal growth hormone secretion.
From left to right: normal stature, gigantism (2.3 m tall) and dwarfism (0.9 m tall).

6. Acromegaly
This means ‘large extremities’ and occurs in adults when there
is excess GH after ossification is complete. The bones become
abnormally thick and there is thickening of the soft tissues.
These changes are most noticeable as coarse facial features
(especially excessive growth of the lower jaw), an enlarged
tongue and excessively large hands and feet.

7. Hyperprolactinaemia
This is caused by a tumour that secretes large amounts
of prolactin. It causes galactorrhoea (inappropriate milk
secretion), amenorrhoea (cessation of menstruation) &
sterility in women and impotence in men.

8. Disorders of the Posterior Pituitary
Diabetes insipidus
This is a relatively rare condition usually caused by
hyposecretion of ADH due to damage to the hypothalamus by,
for example, trauma, tumour or encephalitis. Occasionally it
occurs when the renal tubules do not respond to ADH. Water
reabsorption by the renal tubules is impaired, leading to
excretion of excessive amounts of dilute urine, often more
than 10 litres daily, causing dehydration, extreme thirst
(polydipsia). Water balance is disturbed unless fluid intake is
greatly increased to compensate for excess losses.

9. Disorders of
the thyroid
gland

10. These fall into three main categories:
abnormal secretion of thyroid hormones (T3 and T4)
– hyperthyroidism
– hypothyroidism
goitre – enlargement of the thyroid gland
tumours.
Abnormal thyroid function may arise not only from
thyroid disease but also from disorders of the pituitary or
hypothalamus; in addition, insufficient dietary iodine causes
deficiency in thyroid hormone production.

11. Hyperthyroidism
This syndrome, also known as thyrotoxicosis, arises
as the body tissues are exposed to excessive levels of T3 &
T4. The main effects are due to increased basal metabolic
rate.
The main causes are:
Graves’ disease
toxic nodular goitre
adenoma

12. Graves’ disease (Graves’ thyroiditis)
It affects more women than men & may occur at any age,
being most common between the ages of 30 & 50 years. It is an
autoimmune disorder in which an antibody that mimics the effects
of TSH is produced, causing:
increased release of T3 & T4, signs of hyperthyroidism
goitre as the antibody stimulates thyroid growth
exophthalmos in many cases.

13. Exophthalmos
This is protrusion of the eyeballs that gives the appearance
of staring, which is due to the deposition of excess fat and fibrous
tissue behind the eyes; it is often present in Graves’ disease. In severe
cases the eyelids become retracted & may not completely cover the
eyes during blinking & sleep, leading to drying of the conjunctiva &
predisposing to infection.

14. Toxic nodular goitre
In this condition one or two nodules of a gland that is
already affected by goitre become active & secrete
excess T3 & T4 causing the effects of hyperthyroidism

15. Hypothyroidism
This occurs when there is insufficient T3 & T4
secretion causing:
congenital hypothyroidism in children
myxoedema in adults.
Congenital hypothyroidism
Previously called cretinism, this is a profound deficiency or
absence of thyroid hormones. Unless treatment begins early
in life, mental impairment is permanent and the individual
typically has disproportionately short limbs, a large
protruding tongue, coarse dry skin, poor abdominal muscle
tone and, often, an umbilical hernia.

16. Myxoedema
Prevalent in the elderly & five times more common in females
than males. Deficiency of T3 & T4 in adults results in an abnormally low
metabolic rate. There may be accumulation of polysaccharide substances
in the subcutaneous tissues, especially of the face.
Autoimmune thyroiditis
The most common cause of acquired hypothyroidism is
Hashimoto’s disease. It is more common in women than men, like Graves’
disease, an organ-specific autoimmune condition. Autoantibodies that
react with thyroglobulin & thyroid gland cells develop & prevent
synthesis and release of thyroid hormones causing hypothyroidism.

17. Disorders
of the
Parathyroid
Glands

18. Hyperparathyroidism
Excess secretion of parathyroid hormone
(PTH), usually by benign tumours of a
gland, causes release of calcium from
bones, raising blood calcium levels
(hypercalcaemia). The effects may
include:
Polyuria & Polydipsia
Formation of Renal Calculi
Anorexia & Constipation
Muscle Weakness
General Fatigue.
Hypoparathyroidism
Parathyroid hormone (PTH) deficiency
causes hypocalcaemia, i.e. abnormally low
blood calcium levels, & is much less
common than hyperparathyroidism. There
is reduced absorption of calcium from the
small intestine & less reabsorption from
bones & glomerular filtrate. Low blood
calcium causes:
Tetany, psychiatric disturbances,
paraesthesia, grand mal seizures
in some cases, cataracts (opacity of the
lens) and brittle nails.

19. Disorders of
the adrenal
cortex

20. Hypersecretion of glucocorticoids (Cushing’s syndrome)
Cortisol is the main glucocorticoid hormone secreted by the adrenal cortex.
Causes of hypersecretion include:
•Hormone-secreting adrenal tumours that may be benign or malignant
•Hypersecretion of adrenocorticotrophic hormone (ACTH) by the anterior
pituitary.
•Abnormal secretion of ACTH by a non-pituitary tumour, e.g. Bronchial or
pancreatic tumour.
•Prolonged therapeutic use of ACTH or glucocorticoids, e.g. Prednisolone,
in high doses.

21. The systemic features of
Cushing’s syndrome

22. Hyposecretion of glucocorticoids
Inadequate secretion of cortisol causes
diminished gluconeogenesis, low blood glucose levels,
muscle weakness & pallor. It may be primary, i.e. due
to disease of the adrenal cortex, or secondary due to
deficiency of ACTH from the anterior pituitary.

23. Hypersecretion of mineralocorticoids
Excess aldosterone affects kidney function, with
consequences elsewhere: excessive reabsorption of NaCl & H2O,
causing increased blood volume & Hypertension excessive excretion
of potassium, causing hypokalaemia, which leads to cardiac
arrhythmias, alkalosis, syncope & muscle weakness.
Primary hyperaldosteronism (Conn’s syndrome)
This is due to an excessive secretion of mineralocorticoids,
independent of the renin–angiotensin–aldosterone system. It is
usually caused by a tumour affecting only one adrenal gland.

24. Secondary hyperaldosteronism
This is caused by overstimulation of
normal glands by the excessively high blood
levels of renin & angiotensin that result from
low renal perfusion or low blood sodium.

25. Hyposecretion of mineralocorticoids
Hypoaldosteronism results in failure of the kidneys
to regulate sodium, potassium and water excretion, leading
to:
blood sodium deficiency (hyponatraemia) & potassium
excess (hyperkalaemia) dehydration, low blood volume
& low blood pressure.

26. Chronic adrenocortical insufficiency (Addison’s disease)
This is due to hyposecretion of glucocorticoid &
mineralocorticoid hormones. The most common causes are
development of autoantibodies to cortical cells, metastatic
tumours & infections.

27. The most important effects are:
Muscle weakness & wasting.
Gastrointestinal disturbances, e.g. Vomiting, diarrhoea, anorexia.
Increased pigmentation of the skin, especially of exposed areas,
due to excess ACTH & the related.
Melanin-stimulating hormone secreted by the anterior pituitary.
Listlessness & tiredness.
Hypoglycaemia
Mental confusion
Menstrual disturbances and loss of body hair in women
Electrolyte imbalance, including hyponatraemia, low blood
chloride levels & hyperkalaemia
Chronic dehydration, low blood volume & hypotension.

28. Disorders of
the Adrenal
Medulla

29. Tumours
Hormone-secreting tumours are the main abnormality. The effects
of excess adrenaline (epinephrine) & noradrenaline
(norepinephrine) include:
Hypertension, often associated with arteriosclerosis &
cerebral haemorrhage
Weight loss, Nervousness, Headache
Excessive sweating & alternate flushing & blanching of
the skin
Hyperglycaemia & glycosuria.

30. Phaeochromocytoma:
This is usually a benign tumour, occurring in one or both glands.
The secretion of hormones may be constantly elevated or in intermittent
bursts, often precipitated by raised intra-abdominal pressure,
e.g. coughing or defaecation.
Neuroblastoma:
This is a rare & malignant tumour, occurring in infants &
children under 15 years of age. Tumours that develop early tend to be
highly malignant but in this condition there may be spontaneous
regression.

31. Disorders
of the
Pancreatic
Islets

32. Diabetes mellitus (DM)
This is the most common endocrine disorder
& usually occurs when there is deficiency or
absence of insulin or, rarely, impairment of insulin
activity (insulin resistance).

33. Type I diabetes mellitus/ Insulin-dependent diabetes mellitus
(IDDM)
This occurs mainly in children & young adults; the onset is
usually sudden & can be life threatening. There is severe
deficiency or absence of insulin secretion due to destruction of β-
islet cells of the pancreas. Treatment with injections of insulin is
required. The exact cause remains unknown, although, in most
people, there is evidence of an autoimmune mechanism involving
autoantibodies that destroy the β-islet cells. Genetic predisposition
& environmental factors, including viral infections, are also
implicated.

34. Type II diabetes mellitus
Previously known as non-insulin-dependent diabetes
mellitus (NIDDM), this is the most common form of diabetes,
accounting for about 90% of cases. The causes are multifactorial
& predisposing factors include:
Obesity
Sedentary lifestyle
Increasing age: affecting middle-aged and older people
Genetic factors.