Histo: Endocrine disease Pt.3 Flashcards

1
Q

What is the most common cause of secondary hyperparathyroidism?

A

Renal failure

  • Parathyroid can be enlarged
  • Leads bone disease as with primary disease

Can be caused by any condition with chronic calcium depression

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2
Q

List some causes of hypoparathyroidism.

A
  • Surgical ablation
  • Congenital absence
  • Autoimmune
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3
Q

List some clinical features of hypoparathyroidism.

A
  • Neuromuscular irritability - paresthesia, muscle spasm, tetany
  • Cardiac arrhythmias
  • Seizures
  • Cataracts

CATs go numb

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4
Q

Which cell types constitute the cortex and medulla of the adrenal gland?

A

Cortex = epithelial

Medulla = neural

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5
Q

What are the layers of the adrenal cortex and which hormones do they produce?

A
  • Glomerulosa - aldosterone
  • Fasciculata - glucocorticoids
  • Reticularis - sex steroids
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6
Q

Which conditions causes adrenal hyperfunction?

A
  • Cushing’s syndrome - excess glucocorticoids
  • Hyperaldosteronism (Conn’s)
  • Virilising syndrome - excess androgens
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7
Q

What is the most common cause of Cushing’s syndrome?

A

Iatrogenic - administration of exogenous corticosteroids (leads to adrenal atrophy)

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8
Q

What happens to the adrenal glands in Cushing’s disease?

A

Undergo nodular hyperplasia of the cortex

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9
Q

List 4 endogenous causes of Cushing’s syndrome.

A
  • Cushing’s disease - ACTH producing pituitary adenoma (> 50%)
  • Adrenal adenoma/carcinoma
  • Adrenal hyperplasia
  • Ecotopic ACTH production - small cell lung cancer
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10
Q

What are the clinical features of Cushing’s syndrome?

A
  • Hypertension
  • Weight gain
  • Truncal obesity
  • Moon face
  • Buffalo hump
  • Cutaneous striae
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11
Q

What are the causes of hyperaldosteronism?

A
  • 35% adenoma (Conn’s syndrome)
  • 60% bilateral adrenal hyperplasia
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12
Q

List the two main clinical features of hyperaldosteronism.

A
  • Hypertension
  • Hypokalaemia
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13
Q

What causes virilising syndromes?

A
  • Neoplasms (more commonly carcinoma than adenoma)
  • Congenital adrenal hyperplasia
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14
Q

Describe the pathophysiology of congenital adrenal hyperplasia.

A
  • Autosomal recessive
  • Hereditary defect in an enzyme involved in cortisol synthesis leads to cortisol deficiency
  • This leads to increased ACTH release from the pituitary gland
  • ACTH stimulates adrenal hyperplasia and androgen synthesis
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15
Q

What is the most common cause of CAH?

A

21-hydroxylase deficiency

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16
Q

List three causes of acute primary adrenal failure.

A
  • Sudden withdrawal of corticosteroid treatment
  • Haemorrhage (neonates)
  • DIC associated with sepsis (Waterhouse-Friderichson syndrome)
17
Q

List some causes of chronic primary adrenal failure. (UK)

A
  • Autoimmune (90%)
  • TB
  • HIV
  • Metastatic tumour (lung and breast)
  • Amyloid, fungal infection, haemochromatosis, sarcoid (very rare)
18
Q

What are some secondary causes of adrenal insufficiency?

A
  • Non-functional pituitary adenoma
  • Pituitary/hypothalamic lesions including infarction
19
Q

What are the two types of adrenocortical neoplasm?

A
  • Adenomas - mostly functional, may be associated with Cushing’s syndrome or Conn’s syndrome
  • Carcinomas - rare, more commonly associated with virilisng syndromes than adenomas
20
Q

What are the two types of tumours of the adrenal medulla?

A
  • Phaeochromocytoma
  • Neuroblastoma
21
Q

What is the rule of 10s regarding phaeochromocytomas?

A
  • 10% associated with a familial syndrome (MEN)
  • 10% bilateral
  • 10% malignant
  • 10% oustide the adrenal gland (paraganglioma)

Secrete catecholamine and causes a surgically correctable form of hypertension

22
Q

Define multiple endocrine neoplasia and its inheritance.

A

A group of autosomal dominant conditions resulting in proliferative lesions (hyperplasia, adenoma, carcinoma) of multiple endocrine organs

23
Q

Outline the characteristics of tumours in MEN.

A
  • Tend to occur at a younger age
  • Tend to arise in multiple endocrine organs or may be multifocal within one organ
  • Often preceded by hyperplasia
  • Usually more aggressive than sporadic tumours
24
Q

What are the different types of MEN and the tumours associated with them?

A