Endo Flashcards

1
Q

T1DM blood glucose targets

A

5-7 mmol/l on waking and
4-7 mmol/l before meals at other times of the day

recommend testing at least 4 times a day, including before each meal and before bed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

MEtformin in T1?

A

NICE recommend considering adding metformin if the BMI >= 25 kg/m²

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is De Quarvain’s thyroiditis? Treatment/ management?

A

Subacute thyroiditis (also known as De Quervain’s thyroiditis and subacute granulomatous thyroiditis) is thought to occur following viral infection and typically presents with hyperthyroidism.

There are typically 4 phases;
phase 1 (lasts 3-6 weeks): hyperthyroidism, painful goitre, raised ESR
phase 2 (1-3 weeks): euthyroid
phase 3 (weeks - months): hypothyroidism
phase 4: thyroid structure and function goes back to normal

Investigations
globally reduced uptake on iodine-131 scan

Management
usually self-limiting - most patients do not require treatment
thyroid pain may respond to aspirin or other NSAIDs
in more severe cases steroids are used, particularly if hypothyroidism develops

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Hypopit causes

A
Hypothalamus
		Kallmann syndrome
			Rare genetic, failure to start or complete puberty - anosmia or hyposmia - GnRH deficiency
		Infection
			Meningitis
		Tumour
		Inflammation
	Pituitary stalk
		Mass lesion e.g. craniopharyngioma
		Meningioma
		Carotid artery aneurysm
		Trauma
		Surgery
	Pituitary
		Autoimmune hypophysitis
		Irradiation
		Tumour
		Ischaemia
			DIC
				Snake bite in India assoc with kidney failure
			Sheehan's syndrome - necrosis after postpartum haemorrhage
Pituitary apoplexy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Hypopit features GH

A
Central obesity
		Atyherosclerosis
		Dry wrinkly skin
		Osteoposois
		Hypoglycaemia
		Decreased strength
		Tiredness 
Decreased CO
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

hypopit features LH/FSH

A
Decreased muscle bulk
			Hypogonadism
				Less hair
				Less ejaculate
				Small testes
			Decreased libido
			Low mood
			Tiredness
		Female
			Low libido
			Amen/oligomenorrhea
			Dyspareunia
			Decreased breast tissue atrophy
Osteoporosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

hypopit features not GH and LF/FSH

A
Corticotroph
		Addisons without pigmentation
	Prolactin
		None usually, decreased breast milk production
	Thiotrophs
		Hypothyroidism
	If tumour
		May secrete one of the hormones 
Mass effect - bitemporal hemi and mass effect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Hypopit diagnosis

A

Static (one may be high)
TSH - t4
GH - insluin like growth factor (IGH-1) better marker though (GHRH)
Cortisol
LH/FSH - testosterone/ oestradiol (GnRH)
Prolactin - may be high due to loss of dopamine
U&E - cortisol, Na low from dilution
Low Hb from thyroid normochromic normocytic
Dynamic
ITT - Give insulin - release cortisol, glucose should be induced below2.2 and patient should be symptomatic when cortisol and GH are measured
Short Synacthen - Should supress ACTH and increase glucose?
Arginine and growth hormone-releasing test - should stimulate growth hormone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Hypopit treatment

A
Endo referral - treatment of underlying cause
	Replacement
		Gonadotrophs
			Male
				Testogel
				IM injection
				(buccal monoadhesive tablets)
			Female
				OCP contains enough for maintainence
				Patch or oral 
				Testoesterone - may help
			Gonadotrop therapy to induce fertility in both
		Glucocorticoids
			Hydrocortisone 15mg oral
		Thyrotrophs
			Thyroxine
		Somatotrophs
			Growth hormone - somatotrophin better as less fat gain/ muscle loss
Lactotrophs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Pit adenomas classification

A

Chromophobe (no colour on staining) - 70%, very common e.g. microadenomas (<1cm) which are common. Most likely to be ‘non functioning’ i.e. no hormones secreted so revealed by mass effect or hypopit. Some can secrete
Acidophil 15% Rarer local pressure effect. PRL or GH
Basocphil 15% Rarer local pressure effect. ACHT
** 99% of functioning secrete ACTH, PRL, GH. 30% are non functioning

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Pit adenomas symptoms

A
Hypopituitarism
	Cushings/ Acromegaly/ Prolactinoma
	Mass effect
		Headache
		Visual disturbance
			Bitemporalhemianopia - optic chiasm
			CN III,IV, VI (all muscles of eye) - If infiltrated into cavernous sinus
		Hypothalmic disturbance
			Sleep control
			Temperature control
Diabetes Insipidous (rarely pit cause)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Pit adenoma diangosis

A
Static
		TSH
		Cortisol
		LH/FSH
		GH/ IGF-1
		Prolactin
		ADH
	Dynamic
		Water suppression test - 
			Stage 1 - no drink for 8 hours, measure weight and urine osmolality
			Stage 2 - Give Desmopressin (like ADH) if nephrogenic there will be no response (if nephrogenic give hydrochlorothiazide or amiloride)
		Short acting Synacthen test
		OGTT
	Imaging
MRI - look at mass effect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Pit adenoma treatment

A
Hormone replacement
	Treat Cushings, Acromegal
	If prolactinoma
		Dopamine - cabergoline
	Other
		Transphenoidal resection
		Transfrontal resection if adenoma is supra-stela extension (stellar=saddle)
Radiotherapy (stereotactic) - if recurrent
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Complications of pit adenoma

A

Post op recurrence - need monitoring.
Post op hormone deficiency
Pituitary apopexy
Bleeding in large adenoma, can be life threatening due to sudden hypopituitarism. - headache, menigism, similar to subachacnoid
Urgent steroids and fluid balance and surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Hyperthyroidism causes

A
Autoimmune - 
		Grave's disease 
	Toxic multinodular goitre
		Second most common
		Elderly caused by iodine deficiency
		(Surgery if compressive e.g. dysphagia or dyspnoea)
		(radioactive iodine give
	Toxic adenoma
		Solitary nodule
		(Hot on isiotope scan - malig is white)
	Exogenous Levothyroxine, idoine exess e.g. food contam or contrast medium 
	Ectopic thyroid tissue
	NSAIDs
	Post viral (painful goitre)
	Postpartum
	TB
Amiodarone, lithium (hypo more common)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Symptoms of hyperthyroid

A
General
		Heat intolerance
		Agitation
		Sleep disturbance
		Weight loss
		Hair loss
		Osteoporosis
		Tremor
	GI
		Diarrhoea
		Increased appetite (some may get paradoxical weight gain)
		Sweats
	Cardiac
		Palpations
	GU
		Oligomen/ infert
	Psych
		Psychosis
		Chorea
		Labile emotions
	Opthalmology
		Eye discomfort
		Grittiness
		Tears Photophobia
		Diploria
Less acuity/ colour (more likely if less protrusion as more compression)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Signs of hyperthyroidism

A
Tachycardia
	HBP
	Arrythmia
	Anaemia 
	Lig lad/ retraction
	Goitre/ nodules/ bruit
	Graves
		Pretibial myxoedema - swelling above lateral malleoli
		Exomphalmos
Thyroid acropachy - clubbing, periosteal reaction in limb bones, painful finger and toe swelling
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Complications of hyperthy

A
AF
	HF
	Osteoporosis
	Thyroid storm
	Opthalmology
Gynacomastia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Diagnosis of hyperthyroidism

A
Blood
		Haem
			FBC - normocytic anamia
				In graves can get neutropenia
			Bio chem
			Immunology
				TPO - anti thyroid peroxidase (more hashimoto)
				Antithyroglobulin antibody
				TSH receptor antibody (more graves)
			Special
				T4/T3 (normal or high)
				TSH (low)
		Imagine
Isotope scan - for cause - nuclear scintigraphy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Treatment hyper

A

Rapid contorl of symptoms with propanolol
Carbimazole
Titration with T4 levels
Blockade - high dose and then Thyroxine
Risk of agranularcytosis e.g. temp, sore throat/ mouth ulcers
Radioactive iodine
Most become hypothyroid
Surgical resection - total thyroidectomy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Raised TSH and normal T4

A

subclinical hypothyroidism or treated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

If everything low thyroid

A

sick euthyroid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Use of isotope scan in thyroid

A

Ionie and tachnetiu, pertechnetate
Detect goitre, ectopic thyroid tissue or thyroid mets
Isotope scan - malignant parts tend to have no ‘hot’ nodules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Use of US thyroid

A

Cystic from malignant/ benign nodules - can do with fine needle aspiration

US not enough, also need fNAC and hemithyroidectomy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Hypothyroid causes

A
Autoimmune
		1 -Hashimoto
		2 - Primary atrophic thyroiditis 
	Less common
		Iodine deficiency
		Thyroid resection
		Drugs - amioderone lithium
	Secondary
Hypopituitarism/ pituitary adenoma
26
Q

Symptoms of hypothyroidism

A
Tiredness
	Constipation
	Hair loss
	Lethargy
	Depression
	Weight gain
	Cold intolerance
	Menorrhagia
	Dementia
Myalgia
27
Q

Signs of hypothyroid

A
BRADY
	Reflexes - slow
	Ataxia - cerebella
	Dry thin hair/skin - 
	Yawn - tiredness/coma
	Cold hands
	Ascites - non pitting oedema (hands, lids,feet)
	Round/ puffy fac/ obese
	Defeated demenour
	Immobile - contipation
CCF
28
Q

Complications of hypo

A
Preggers
		PPH
		Eclampsia
		Anaemia
		Prematurity
	Myxiedema coma
High assoc with CCF and dementia untreated0.
29
Q

Diagnosis hypothyroids

A
TSH, T4, T3
	TPO or TGB
	Isotope scan
	Cholesterol and TG raised
Macrocytosis - rarely anaemia
30
Q

Treatment hypothyroidism

A

Oral levothyroixine - Aim to Keep TSH normal, small increase has log effects on TSH - tell patients
Elderly - start low due to risk of Angina/MI
Excess thyroxine can cause osteoporosis and AF so monitor

31
Q

Addisons Causes

A
Primary (loss of cortico and mineralo)
		80% autoimmune adrenalitis (may also affect thyroid or panc)
		TB
		Mets
		HIV
		SLE
		Antiphospholipid syndrome
	Low ACTH
		Rare
		Hypopituitarism
		Pituitary adenoma
		Iatrogenic: Steroid withdrawal, adrenectomy (kidney)
In above mineralo is normally fine
32
Q

Addisons sympoms and signs

A
Symptoms
	Pigmentation - high ACTHTiredness/ lethargy/ coma
	Low BP
	Hypoglycaemia - dizziness/ confusion
	Weakness
	Weight loss/ anorexia - muscle loss
	Amennorrhea/ ED
	Hair loss
	Myalgia/ arthraligua
	Depression/ psychosis
	GI abdo pain and vomiting (high K)
Signs
	Low BP - postural too
	Tachy
	Low BM
Pigmentation
33
Q

AD Diagnosis

A

Low Na and high K due to loss of mineralocorticoid
Hypercalcaemia
Hypoglcaemia
Metabolic acidosis (loss of aldosterone and less Na resorbition in DCT)
ACTH 9am
Short synacthen test
Should result in increased cortisol within 30mins (Check before too)
Pos = low cortisol - to do with rise. Why not just adrenal
If not do long test between secondary and privary. Higher dose and look more than 1 hr. Secondary = normal response but lower
Autoantibodies (21 hydroylase adrenal antibodies), if not then TB, mets, HIV, SLE
Plasma renin & aldosterone
AXR/ CXR if thinking TB

34
Q

AD treatment

A

teroid replacement
Hydrocortisone 20mgish e.g. 10/5/5 at diff times
Late can cause insomnia
Fludrocortisone

Patient info
	Steroid card
	Double in febrile or illness or stress
	Increase with strenous activity
	Teach IM in case of vomiting
Follow up yearly - risk of associated pernicious anaemia
35
Q

hyperaldosteronism causes

A

2/3 - Aldosterone secreting adrenal adenoma/ Conn’s (30-50years)
1/3 - bilateral adrenal hyperplasia (idiopathic)
Others
Adrenal carcinoma
Glucocorticoid remediable aldosteronism (GRA) (hyperresponsive to ACTH (normally only angiotensin II)
ACTH regulated aldosterone
Secondary hyperaldosteronism
Renal artery stenosis/ diuretic, CCF, Hepatic failure
High renin (low perfusion)
High aldosterone
Bartter’s syndrome
Leaky loop of henley
Polydipsia
Polyuria
(volume depletion = high renin)
Genetic Aut recessive
Failure to thrive in chuildren, poly uria and polydipsia
Treatment - K replacement, NSAIDs ACEi

36
Q

hyperaldosteronism symptoms

A

Hypertension (may be normal), Parasthesia, weakness, cramps polyuria/polydipsia (high Na),

37
Q

Hyperaldosteronism diag

A
High Na
	Low K (normal in 20%)
	U &amp;Es
	Adrenal vein sampling - catheter to look if hormone production is bilateral or not
	Check Renin aldosterone levels
GRA - genetic testing
38
Q

Hyperaldosteronism treatment

A

Conn’s- surgery/ spirono pre op
Adrenal hyperplasia - spirono or amiloride
GRA
Steroids should fix - can remain with high BP so give spirono

39
Q

MEN symptoms

A

MEN1
Parathy
Pancreas
Pituitary

MEN2a
Thyroid medulla
Parathyroid
Pheo

MEN 2b
	Thyroid
	Pheo
	Marfans
Mucosal neuroma
40
Q

Hyperparathyroidism causes

A

• Primary - Solitary adenoma =80%, 20% bilateal hyperplasia, PT cacer
• Secondary - Hypocalcaemia e.g. renal failure, Lit Vit D intake
• Tertiary - prolonged hypocalcaemia leading to autologous PTH secretion and a raised Ca
Malignant hyperpara - PTHrP by SCC, breast and RCC (low PTH in assays)

41
Q

Hyperparathyroidism symp

A

• Stones, thrones, abdominal groans, bones, psychiatric overtones
• Stones = renal calculi
• Thrones = polyuria (polydipsia) and constipation
• Groans = Abdominal pain
• Painful bones = pain, pathological fractures, osteoporosis
Psychiatric = lethargy, depression, psychosis, delerium, ataxia

42
Q

Sings of Hyperpara

A

• Dehydration (paradoxical to polyuria)

HBP!!

43
Q

Investigation of hyperpara

A

• Serum Ca and PTH
• PO4 (usually low as PTH increases excretion)
• Increased ALP from bone activity
• Us and Es
• Osteitis fibrosa cystica shows as suboeriosteal erosions, cysts or tumours of phalagnes and acro osteolysis, may be operpper pot
• DEXA
US and MIBI (isotope) to localise adenoma

44
Q

Treatment of hyperpara

A
• Medical
		○ Mild
			§ Fluid
			§ Ca
			§ Vit D
			§ Avoid thiazides
	• Surgical removal of adenoma - indicated if high Ca or complications
Cinacalcet can sensitise PTH secretion to Ca and decrease it
45
Q

Symptoms of hypoparathyroid

A

Hypocalcaemia
Tetany/ chorea/ spasm

	SPASMODIC Other autoimmune features
46
Q

Investigation

A

High PO4
Low Ca
Normal ALP

47
Q

treatment hypopara

A

Ca supp and calcitriol or synthetic PTH

48
Q

Hypocalcaemia causes

A
High PO4
			Renal failure
			Hypo parathyroid
			Rhabdo
			hypomagnesaemia
		Normal PO4 or low
			Pancreatitis
			Vit D deficiency
			Osteomalacia
			Over hydration
Resp alk (less ionised Ca due to increase pH)
49
Q

Hypocalcaemia symptoms and signs

A
Symptoms
		Spasm
		Periorbital parasthesiae
		Anxiety/ irritation
		Seizure
		Muscle tone increased
			Constipation
			Dysphagia
			Dyspnoea
		Orientation impaired
		Dermatitis (atopic)
		Impetigo herpeticum (emergency)
		Chvostek sign
		Cardiomyopathy (long QT)Chorea
		Catact (chronic)
Signs - Chvostek's - tap on parotid and facial nerve twitches
Trousseau's sign - inflate cuff and wrist and fingers flex
50
Q

Emergency presentation symptoms of hypercalcaemia

A

Usually but also
Confusion
Pyrexia
Cardiac arrest (dec QT)

51
Q

Causes of gonad failure in men

A
Primary
		Teticular failure from
			Local trauma
			Torsion
			Chemo/irradiation
			Post-orcitis e.g. mumps, HIV, leptrsoy
			Renal failure
			Cirrhosis
			Alcohol excess (toxic to Leydig)
			Klinefelters
				Delayed sexual development 
				Small testes 
				Gynaecomastia
Androgen insensitivity syndrome (look female)
	Secondary
		Hypopit
		Prolactinoma
		Kallman's syndrome (isolated (GNRH hormone)
		Age
52
Q

Describe Klinefelter’s syndrome

A

Klinefelter’s syndrome is associated with karyotype 47, XXY

Features
	• often taller than average
	• lack of secondary sexual characteristics
	• small, firm testes
	• infertile
	• gynaecomastia - increased incidence of breast cancer
	• elevated gonadotrophin levels
Diagnosis is by chromosomal analysis
53
Q

Describe Turner’s syndrome

A

Turner’s syndrome is a chromosomal disorder affecting around 1 in 2,500 females. It is caused by either the presence of only one sex chromosome (X) or a deletion of the short arm of one of the X chromosomes. Turner’s syndrome is denoted as 45,XO or 45,X

Features
• short stature
• shield chest, widely spaced nipples
• webbed neck
• bicuspid aortic valve (15%), coarctation of the aorta (5-10%)
• primary amenorrhoea
• cystic hygroma (often diagnosed prenatally)
• high-arched palate
• short fourth metacarpal
• multiple pigmented naevi
• lymphoedema in neonates (especially feet)
There is also an increased incidence of autoimmune disease (especially autoimmune thyroiditis) and Crohn’s disease

From

54
Q

Describe MODY

A
MODY - mat onset dm of young
	Genetic production of insulin impaired
	Similar to T2DM
	Prog to comp such as DKA
	Hepatic nuclear factor 1 alpha
	Give sulfonylureas as very sensitive
	<25ywars
Fx of early onset present
55
Q

Describe LADA

A
Latent Autoimmune DM of adulthood - LADA
	Assoc with graves
	Weight loss, poly dip, poly urea
	Don’t require insulin in early stages
	Similar to T1
Islet failure not resistance
56
Q

Causes of hypoglycaemia

A
DM
	EXPLAIN
		EXogenous drugs - body builders, alcohol binge with no food, ACEi
		Pit insufficiency
		Liver failure
		Addisons
		Islet cell tumours
Non-pancreatic neoplasms e.g. fibrosarcoma
57
Q

Insulinoma diagnosis and treatment

A
Whipple's triad
		Symptoms with fasting or exercise
		Recorded hypoglycaemia with symptoms
		Symptoms relieved by glucose
	May be with MEN1
	CT/MRI and hypoglycaemia and insulin on prolonged fast
	Treatment
Excision
58
Q

Acromegaly cause

A

In acromegaly there is excess growth hormone secondary to a pituitary adenoma in over 95% of cases. A minority of cases are caused by ectopic GHRH or GH production by tumours e.g. pancreatic

59
Q

Acrogmegaly features and comp;lications

A

• coarse facial appearance, spade-like hands, increase in shoe size
• large tongue, prognathism, interdental spaces
• excessive sweating and oily skin
• features of pituitary tumour: hypopituitarism, headaches, bitemporal hemianopia
• raised prolactin in 1/3 of cases → galactorrhoea
• 6% of patients have MEN-1
Complications
• hypertension
• diabetes (>10%)
• cardiomyopathy
colorectal cancer

60
Q

investigations acromegaly

A

OGTT with serym GH or IGF-1

Pit MRI

61
Q

Treatment

A

Transphenoidal surgery first line
Somatostatin (inhibirs GH realease) analogue as adjunct e.g. octreotide
Dopamine agonist (bromocriptine)
Pegvisomant (GH receptor antagonist)