Diseases of Endocrine System Flashcards

1
Q

where is the pituitary gland situated?

A

in the Sella Turcica

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2
Q

how many parts of the pituitary gland are there and what percentage of the pituitary gland does it pertain?

A

Anterior and Posterior

75% = anterior lobe
25% = posterior lobe
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3
Q

what is the function of the Adenohypophysis?

A

produces

  • prolactin
  • adenocorticotropic
  • growth hormone
  • thyroid stimulating
  • follicle-stimulating
  • luteinsing
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4
Q

what is the function of the Neurohypophysis?

A

Produces

  • Oxytocin
  • antidiuretic peptide
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5
Q

what are the causes of anterior pituitary hypo function?

VITAMIN D3

A
  • Vascular - Infarction
  • Inflammation - granulomatous
  • Trauma
  • Autoimmune - Pituitary autoimmune disease
  • Metabolic
  • Infection
  • Neoplasia - Non-secretory adenoma, metastatic carcinoma
    D3 - Doctors
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6
Q

what type of primary pituitary tumours is most common?

A

most = adenomas

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7
Q

what are the types of Anterior Pituitary Adenomas?

A
  • Prolactinoma - commonest, galactorrhoea and menstrual disturbance
  • Growth Hormone Secreting - Gigantism in children, acromegaly in adults
  • ACTH secreting - Cushing’s syndrome
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8
Q

where is the thyroid located?

A

located at the level of 5th - 7th vertebra

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9
Q

how does the thyroid get to its position?

A
  • The main part migrates from foregut to anterior neck

- Ultimobranchial body forms in branchial arches and fuses with main gland laterally

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10
Q

what is Chronic Lymphocytic Thyroiditis?

A

Autoimmune chronic inflammatory disorder that affect females more than males with a peak age at 59 years old

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11
Q

what are the increased risks of Hashimoto’s?

A
  • 80-fold increased risk of thyroid lymphoma

- Increased risk of papillary carcinoma of the thyroid

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12
Q

what is Diffuse Hyperplasia (GRAVES DISEASE)

A

An autoimmune process, a diffuse hyperplasia of the follicular epithelium

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13
Q

what is the cause of most cases of hyperthyroidism?

A

responsible for 80% of cases is diffuse hyperplasia (Graves’ Disease)

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14
Q

what are the physical findings of GRAVES’ DISEASE?

A
Pretibial myxoedema, 
hair loss,
 wide-eyed stare or proptosis, 
tachycardia,
 hyperactive reflexes
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15
Q

what are the clinical findings of Diffuse Hyperplasia?

A

Thyroid diffusely enlarged
T3 and T4 elevated.
TSH markedly suppressed
Thyroid autoantibodies - thyroid stimulating immunoglobin

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16
Q

what is Multinodular Goitre?

A

Enlargement of thyroid +/- nodularity

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17
Q

what is multinodular goitre often mistaken for?

A

Large ‘dominant’ nodules may be mistaken clinically for thyroid carcinoma

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18
Q

what is follicular adenoma?

A

Benign encapsulated tumour with evidence of follicular cell differentiation

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19
Q

what groups are more likely affected by follicular adenoma?

A

Females > Males

wide age range, usually fifth to sixth decade

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20
Q

what are the % of malignant tumours of the thyroid?

A
  • 1.1% of new cancers
  • 0.32% of cancer deaths
  • 85% are differentiated thyroid carcinoma
  • 5-9% are medullary carcinoma
  • 1-2% are anapaestic carcinoma
  • 1-3% are malignant lymphoma
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21
Q

what is the commonest type of thyroid carcinoma?

A

papillary carcinoma - 70%

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22
Q

who is most at risk for papillary carcinoma?

A

Female predominance 2.5:1

wide age range mean 43 years

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23
Q

what is papillary Carcinoma?

A

Familial, autosomal dominant non-medullary thyroid carcinoma

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24
Q

what % of all thyroid cancer are follicular carcinomas?

A

10-20% of all thyroid cancers

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25
how do most follicular carcinoma present?
90% present with solitary nodule in thyroid
26
what are the groups most affected by Hurthle Cell Carcinomas?
Median age 53 (range 24-85 years) | Sex ratio of F:M 7:3
27
what is the main difference between follicular carcinoma?
Hurthle cell carcinomas have a significant incidence of cervical lymph node metastases compared to follicular carcinoma
28
what are the common haematogenous sites for hurthle cell carcinoma?
Bone, Liver and Lung
29
what is Primary Hyperparathyroidism?
excessive secretion of parathyroid hormone from one or more glands (PHPT)
30
what is secondary Hyperparathyroidism?
hyperplasia of glands with elevated PTH in response to hypocalcemia
31
what is tertiary hyperparathyroidism?
in association with longstanding secondary hyperparathyroidism
32
what is the incidence of primary hyperparathyroidism?
1. 25 - 28 cases per 100,000 population | 2. Caucasian women over 60 - 190/100,000
33
what is the pathogenesis of primary hyperparathyroidism?
1. Aging, tumorigenesis in general 2. Association with ionising irradiation 3. MEN 2a
34
what are the signs of Hypercalcemia/Hyperparathyroidism? Bones, Stones, Groans, Moans
1. Painful bones - painful bone condition 2. Renal Stones - Kidney Stones 3. Abdominal Groans - Gi symptoms: Nausea, Vomiting, Constipation, Indigestion 4. Psychiatric Moans - Effects on nervous system: lethargy, fatigue, memory loss, psychosis, depression
35
what is parathyroid Adenoma?
An encapsulated benign neoplasm of parathyroid cells
36
what is parathyroid adenoma associated with?
has an association with MEN1 and MEN2 syndrome and hyperparathyroidism and jaw tumour syndrome
37
what occurs during secondary and tertiary hyperparathyroidism
non-neoplastic increase in parathyroid parenchymal cell mass within all parathyroid tissue with a known stimulus
38
what is parathyroid carcinoma?
malignant tumour derived from parathyroid parenchymal cells
39
what is the survival rating for parathyroid carcinoma?
50% 10 year survival
40
what are the exogenous causes of Cushing's Syndrome?
excessive glucocorticoid medication
41
what are the endogenous causes of Cushing's Syndrome?
Adrenal Cortical tumours, adrenal cortical hyperplasia, ACTH secreting pituitary adenoma
42
what is cushing's syndrome due to?
due to prolonged exposure to cortisol
43
what are the signs and symptoms of cushing's syndrome?
``` Hypertension moon face central obesity buffalo hump weak muscles osteoporosis insomnia excess sweating mood swings headaches chronic fatigue women may have hirsutism and irregular menstruation ```
44
what is Conn's syndrome?
EXCESS PRODUCTION OF THE HORMONE ALDOSTERONE LEADING TO LOW RENIN LEVELS
45
What are the causes of primary Conn's syndrome?
adrenal cortical hyperplasia, adenoma familial hyperaldosteronism
46
what are the causes of secondary Conn's syndrome?
low circulating volume | poor renal circulation
47
who is most at risk of getting conns syndrome?
Women > Males | 30-50 year olds
48
what are the signs and symptoms of Conn's syndrome?
``` High BP Headache Muscular weakness Muscle spasms Cardiac ARRYTHMIAS Excessive urination ```
49
what is Addisons Disease?
Adrenal cortical insufficency
50
what are the causes of primary addisons disease?
Adrenal dysgensis, adrenal destruction. autoimmune adrenalitis TB
51
what are the causes of secondary addisons disease?
Failure of ACTH secretion
52
what are the triad of symptoms for addisons disease
1. Hyperpigmentation 2. Postural Hypotension 3. Hyponatraemia
53
how do you treat addisons disease?
treat with long term steroid replacement
54
what is adrenal cortical nodule?
Benign non-function nodules of adrenal cortex
55
what % of the population is affected by adrenal cortical nodules?
between 1.5% and 3% of the population
56
Which groups are affected by adrenal cortical nodules?
Elderly, hypotensive and diabetic patients
57
how was adrenal cortical nodules discovered?
it was incidentally discovered on radiographic studies
58
what is adrenal cortical adenoma?
A benign neoplastic proliferation of adrenal cortical tissue
59
what is the incidence of adrenal cortical adenomas in the population?
incidence from 1-5% of the population
60
what are the signs and symptoms of adrenal cortical adenoma?
symptoms are related to endocrine hyper function -aldosterone-producing tumours cause Conn's syndrome cortisol producing tumours cause cushing's syndrome - rare tumours cause virilisation
61
what is adrenal cortical carcinoma
its the malignant counterpart of adrenal cortical
62
What are the signs and symptoms of adrenal cortical carcinoma?
symptoms are related to hormone excess | abdominal mass is present
63
what is the survival rate for adrenal cortical carcinoma?
5 year survival about 70% | the prognosis is age and stage dependent
64
what is phaeochromcytoma?
Catecholamine-secreting tumour arising from adrenal medulla
65
what is the rate of pheochromocytoma is the population?
8/100000 are affected
66
what is the rule of 10's in relation to phaeochromocytoma?
``` it means 10% of tumours are: 10% bilateral 10% extra-adrenal 10% malignant 10% familial and q0% in children ```
67
what are some associations with pheochromocytoma?
MEN2A/2B Von Recklinghausen's disease von Hippel/indau disease
68
what are some symptoms of phaeochromocytoms?
hypertension palpitations headaches anxiety
69
what are some clinical features of pheochromocytoma?
elevated urine catecholamines, adrenaline and noradrenaline
70
what is the prognosis of benign pheochromocytoma?
excellent prognosis when its benign and properly managed surgically
71
what is the prognosis of malignant phaeochromocytoma?
not as good of a prognosis as tumour may pursue an aggressive course