Breast and endocrine Flashcards

1
Q

Causes of gyenacomastia

A

METOCLOPRAMIDE

Metaclopramide/ Methyldopa
Ectopic oestrogen
Trauma skull/ Tumour breast/ testes
Orichitis
Cushings/ cimetidine
Liver cirrhosis
Obesity (increased oestrogen in fat tissue)
Paraplegia/ puberty/ physiological (new borns-oestrogen from mom)
RA
Acromegaly/ Anabolic steroids
Mumps (testicular failure)
Isoniazide
Digoxin/ Digitalis
Ethionamide

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2
Q

What is the pathophysiology of gynacomastia

A

Increased ratio of oestrogen: androgens in the body

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3
Q

What are androgens

A

Sex hormones that help with puberty

Testosterone
androstendione
Dihydroepiandrostendione (DHEA)
DHEA-sulphate

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4
Q

Treatment of primary hyperparathyroidism due to a parathyroid adenoma

A

Surgical excision

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5
Q

Cause of zollinger-ellison syndrome

A

Pancreatic gastrinoma made of pancreatic G cells which secrete gastrin

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6
Q

What are the 3 ohases of gastric acid secretion

A

Cephalic
gastric
intestinal

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7
Q

What are the stimulants for the 3 phases of gastrin secretion

A

cephalic= sight/ smell of food
gastric= stomach distension
intestinal= food enters duodenum

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8
Q

What nerve provides the parasympathetic supply to give gastrin secretion

A

Vagus nerve

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9
Q

Describe the events of cephalic phase of gastric secretion

A

sight/ smell of food= vagal stimulation
G-cells of antrum of stomach stimulated
G-cells secrete gastrin
Gastrin stimulates gastric acid/ pepsin/ histamine release from parietal cells/ mast cells

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10
Q

Describe the events of gastric phase of gastric secretion

A

food enters stomach
causes distension of stomach
vagal stimulation from distension
gastrin secreted
gastric acid produced (60% in gastric phase)

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11
Q

T/F: Histamine release inhibits gastrin secretion

A

FALSE- Histamine release stimulates gastric acid secretion

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12
Q

T/F: Somatostatin inhibits gastric acid production

A

TRUE- somatostatin acts directly on parietal cells to inhibit gastric acid secretion

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13
Q

What cells are involved in insulinoma

A

Beta islet cells of pancreas

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14
Q

What is Whipples triad

A

-attacks brought on by fasting
-hypoglycaemic during attacks
-attacks improve with administration of glucose

Triad present in those with an insulinoma-have attacks of lightheadedness, mood swings, unconsciousness (sx of hypo)

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15
Q

What cells are involved in glucagonoma

A

Alpha islet cells of pancreas

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16
Q

Commonest causes of thyrotoxicosis

A

Graves
multinodular toxic goitre
solitary toxic nodule

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17
Q

Which condition causes chronic fibrosis of the thyroid gland

A

Reidel’s thyroiditis

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18
Q

How to differentiate between Graves and other causes of thyrotoxicosis

A

Graves has:
eye signs (exophthalmos, ophthalmoplegia)

pretibial myxoedema

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19
Q

Describe the conditions associated with MEN type 1

A

3 P’s:

Pituitary adenoma
Parathyroid hyperplasia
Pancreatic islet cell tumours

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20
Q

Which MEN syndromes are associated with pheochromocytomas

A

MEN type 2A + 2B

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21
Q

Which MEN syndrome is associated with phaochromcytomas, medullary thyroid cancer, parathyroid hyperplasia

(2P’s 1M)

A

MEN 2A

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22
Q

What conditions are associated with MEN 2B (1 P, 3Ms)

A

phaochromcytomas
medullary thyroid cancer
marfanoid appearance
mucosal neuromas (neurofibramatosis)

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23
Q

What is the gene mutation associated with the MEN syndromes

A

RET proto-oncogene

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24
Q

What is the inheritance pattern for MEN syndrome

A

Autosomal DOMINANT (because MEN like to dominate)

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25
Describe the 2 ways in which chronic renal failure leads to hypocalcaemia
1: renal failure= reduced activation of Vit D = reduced Ca absorption in the intestines 2: renal failure= phosphates not excreted= increased phosphates in the blood bind to free Ca= reduced free Ca in blood
26
What histology would you see in papillary thyroid carcinoma
orphan annie nuclei psammoma bodies
27
What type of thyroid ca is common in young women with prev head/ neck irradiation
papillary Ca
28
What condition causes: raised serum calcium low urinary calcium normal/ raised PTH hypermagnesiemia
Familial Hypocalciuric Hypercalcaemia
29
What is the inheritance pattern for FHH
Autosomal dominant
30
Pathophysiology of FHH
FHH due to non-functioning Ca sensing receptor (CaSR) CaSR found on parathyroid + kidneys Parathyroid: -normally detects serum Ca and regulates PTH secretion via -ve feedback FHH= CaSR not working= PTH secreted without feedback despite high Ca Kidneys: -normally allows for Ca excretion in kidneys and stops reabsorption FHH= Ca not excreted in kidneys= low Ca levels in urine (hypocalciuric)
31
Management of symptomatic FHH
calcimimetics + pamidronate (bisphosphonates not used)
32
What is a complication of FHH and how is it managed
recurrent pancreatitis Mx= parathyroidectomy
33
Which type of cancer can cause high Ca low phosphate
SCC lung causes paraneoplastic syndromes= PTH mimicking peptide secreted
34
Indications for thyroid surgery
4C's: cosmesis compression (trachea/ oesophagus) carcinoma control (of thyrotoxicosis)
35
How can follicular carcinoma and adenoma be distinguished/ diagnosed
thyroid lobectomy + histology to confirm
36
Management of follicular carcinoma
total thyroidectomy (if confirmed by histology)
37
Where does papillary thyroid cancer mets to
(lymph spread) cervical lymph nodes
38
Where does follicular thyroid cancer mets to
brain bone lungs
39
Another name for MEN 2A syndrome
Sipples syndrome
40
Commonest causes of primary hyperparathyroidism
parathyroid adenoma parathyroid hyperplasia carcinoma
41
What are the factors associated with anaplastic thyroid Ca
F>M iodine deficiency history of multinodular goitre
42
Sx of anaplastic thyroid ca
hoarse voice thyroid mass (rapid growing) dysphagia
43
Where does anaplastic thyroid Ca mets to
brain bone lungs
44
Management of anaplastic Thyroid Ca
palliative (doxorubicin/ cisplatin)
45
Biochem difference between osteoporosis and pagets disease: (Ca, Phos, PTH, ALP levels)
Pagets: ALP= very raised Ca, Phos, ALP= normal osteoporosis: All normal
46
What other conditions is Hashimotos associated with?
pernicious anaemia coeliacs thyroid lymphoma
47
Which cancers can cause paraneoplastic syndrome
small cell lung ca bronchial carcinoma Thymic tumours medullary thyroid cancer islet cell tumours of pancreas
48
Cushings disease vs syndrome
Disease= pituitary adenoma causing raised ACTH= causes increased cortisol from adrenal Syndrome= increased cortisol from adrenal (any cause- pituitary adenoma/ steroid use/ paraneoplastic tumours/ ectopic sources)
49
Treatment of hyperthyroidism in pregnancy
1st trimester= PTU after 1st trimester= carbimazole PTU =not after 1st tri= affects liver development Carbimazole= not in 1st tri= teratogenic Not surgery= anaeasthetic risk to fetus
50
What condition causes secondary HTN hypernatraemia hypokalaemia metabolic alkalosis
Conns (Hyperaldosteronism)
51
Where is aldosterone made and where does it act
Aldosterone made: zona glomerulosa of adrenal cortex acts: DISTAL convoluted tubule + collecting ducts kidneys
52
Management options for Conns
Spironolactone (aldosterone antagonist) adrenalectomy
53
What are the biochemical disturbances found in Addison's disease
addisons= adrenal insufficiency hyponatraemia hyperkalaemia hypercalcemia
54
What condition causes hypercalcaemia cough/ SOB hilar lymphadenopathy afro-carribeans affected 30-40s
Sarcoidosis
55
Management of Sarcoidosis
Steroids
56
Investigations for Conns
Bloods (raised aldosterone) Adrenal scintigraphy CT/ MRI adrenals Diurnal/ positional aldosterone levels
57
What are the antibodies found in Hashimotos thyroiditis
anti-microsomal/ anti-thyroid peroxidase anti- thyroglobulin antibodies
58
What is a complication post bilateral adrenalectomy for cushings syndrome
Nelsons syndrome
58
what type of hernia is associated with congenital hypothyroid
umbilical hernia in children
59
Pathophysiology of Nelsons syndrome
Resection of both adrenals = reduced cortisol -ve feedback= pituitary secretes ACTH= increasing ACTH production causes swelling of pituitary pituitary swelling causes sx= headaches, cranial nerves affected
60
What enzyme deficiency causes congenital adrenal hyperplasia
21-hydroxylase deficiency
61
Pathophysiology of CAH
21-hydroxylase deficiency= not enough cortisol produced= increased ACTH released= increased precursors of cortisol= these precursors are used to make testosterone instead in females= leads to hermaphrodite in males= precocious sexual maturation
62
First line investigation for sx of acromegaly
Insulin like growth factor levels