Diseases of the endocrine system Flashcards

1
Q

Primary pituitary tumours

A
  • most are adenomas, benign
  • if the tumour is functional, the clinical effect is secondary to the hormone being produced
  • Local effect is due to pressure on optic chiasma
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2
Q

Types of anterior Pituitary adenoma

A

1) Prolactinoma – commonest - galactorrhoea, menstrual disturbance
2) Growth hormone secreting – gigantism in children, acromegaly in adults
3) ACTH secreting – Cushing’s syndrome

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3
Q

Thyroid gland

A
  • Located at the 5,6,7 level of cervical vertebrae
  • recurrent laryngeal nerve directly behind
  • In front of trachea
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4
Q

Hashimoto’s thyroiditis

A
  • Autoimmune chronic inflammatory disorder = diffuse enlargement and thyroid autoantibodies and many patients become hypothyroid
  • F>M, peak age = 59
  • Lymphoid follicles form
  • Increased risk of papillary carcinoma of thyroid
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5
Q

Grave’s disease

A
  • Diffuse hyperplasia
  • Autoimmune process resulting in clinical hyperthyroidism and diffuse enlargement and hyperplasia of the follicular epithelium
  • Peak in late 30, F>M
  • Thyroid autoantibodies elevated
  • Orange peel skin, hair loss, tachycardia
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6
Q

Multinodular goitre

A
  • Enlargement of thyroid with varying degrees of nodularity; with multiple hyperplastic nodules involving the gland.
  • Most patients are euthryoid
  • Tracheal compression/ dysphagia may develop
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7
Q

Follicular adenoma

A
  • Benign encapsulated tumour affecting follicular epithelium with evidence of follicular cell differentiation
  • F>M, late 50’s peak
  • Painless neck mass
  • Usually cold nodule on radioactive iodine imaging
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8
Q

Malignant tumours of Thyroid %

A

5-9% are medullary carcinoma
1-2% are anaplastic carcinoma
1-3% are malignant lymphoma
85% of thyroid malignant tumours are well differentiated thyroid carcinoma.

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9
Q

Papillary carcinoma

A
  • > 70% of thyroid cancers
  • mean age 43, 2.5 x F>M
  • Appears as an irregular solid or cystic mass or nodule in a normal thyroid parenchyma
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10
Q

Papillary carcinoma aetiology

A
  • Familial inheritance - autosomal dominant non-medullary thyroid carcinoma
  • Associated with Cowden/s syndrome and FAP
  • Can be result of exposure to radiation
  • RET or NTRK1 genes are activated or RAS mutation
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11
Q

Papillary carcinoma macroscopic appearance

A
  • ill defined, infiltrative, some encapsulated, may be cystic, granular. Finger like projections, nuclei crowded, clear.
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12
Q

Follicular neoplasms

A
  • Follicular adenoma
  • RAS mutation
  • Hurthle cell carcinoma = potential lymph node carcinoma
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13
Q

Primary hyperparathyroidism

A
  • excessive secretion of parathyroid hormone from one or more glands, pathology lies within gland.
  • Signs = arterial HT, hypercalcaemia, decreased renal function
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14
Q

Primary hyperparathyroidism aetiology

A
  • Single adenoma (90%)
  • aging
  • ionizing radiation
  • Men 2a syndrome
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15
Q

Secondary hyperparathyroidism

A
  • hyperplasia of glands with elevated PTH in response to hypocalcaemia
  • increase in parathyroid parenchymal cell mass
  • Common in patients with renal failure and on dialysis
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16
Q

Parathyroid adenoma

A
  • From primary hyperparathyroidism
  • An encapsulated benign neoplasm of parathyroid cells – that secrete parathyroid hormone.
  • Single enlarged parathyroid gland
  • Symptoms of hypercalcaemia
17
Q

Parathyroid carcinoma

A
  • Rare 1% of primary hyperparathyroidism
  • PTH and calcium levels raised
  • Metastasis uncommon so treated with surgery
18
Q

Cushing’s Syndrome

A
  • Zona fasciculata of adrenal cortex
  • Prolonged exposure to cortisol
  • Caused by excessive glucocorticoid medication. adrenal cortical tumours
19
Q

Cushing’s Syndrome presentation

A

Hypertension, moon face, central obesity, muscle weakness, osteoporosis, insomnia, excess sweating, mood swings, headaches, chronic fatigue, women – increased hair growth (hirsutism), irregular menstruation

20
Q

Conn’s syndrome

A
  • Zone glomerulosa of adrenal cortex
  • Hyperaldosteronism, can be primary and secondary
  • Excessive aldosterone leads to low renin levels
21
Q

Conn’s syndrome aetiology and presentation

A

Aetiology - adrenal cortical hyperplasia/adenoma

Presentation - Hypertension, muscle weakness ad spasms

22
Q

Addison’s disease

A
  • Primary adrenal cortex insufficiency adrenal destruction
  • Secondary adrenal cortex insufficiency due to failure of ACTH secretion
  • Autoimmune form most common
  • Triad: hyperpigmentation, postural hypotension, hyponatraemia
23
Q

Pheochromocytoma

A
  • Catecholamine-secreting tumour arising from adrenal medulla
  • Elevated urine catecholamines, adrenaline, noradrenaline
  • Excellent prognosis when benign
  • Symptoms of hypertension, palpitations, headaches, anxiety
  • Rule of 10 - 10% malignant