Endo Flashcards

1
Q

Pregnant patient - TFTs

A

TSH can be mildly suppressed in up to 13% of pregnancy in first trim. T3 and T4 can slightly increased too due to HCG stimulation

T-binding globulin has twofold increase due to reduced hepatic clearance and increased synthesis due to oestrogen

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

Best management for hirtuism in PCOS

A

weight loss
5% weight loss has 40% improvement of hirtuism

Crypterone acetate& ethinyloestradiol or COCP can be used

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

Patient collapses. Raised c peptide, hypoglycemic

A

Could be sulphonylurea abuse, esp if family member has T2DM
Could be insulinoma, but rare
Could be Addisonian crisis - low BP, hyperkal hyponat

Insulin abuse would have suppressed c peptide

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

Management of prolactinoma

A

Cabergoline, very effective, unlikely to need surgery

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

Management for acromegaly

A

Treat with Somatostatin Analogues (Octreotide) then transphenoidal surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Patient with hyperthyroidism on amiodarone due to paroxysmal VT. On Doppler USS blood flow is increased

Management

A

Start carbimazole 40mg OD

Amiodarone should ideally be stopped but given the VT this is difficult

USS with increased blood flow is Type 1 amiodarone hyperthy, treat with carbimazole
decreased blood flow is Type 2, corticosteroids

Type 2 is usually with no underlying disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Thyrotoxicosis in pregnancy…management

A

propylthiouracil in first trim, then carbimazole

If painful goitre, raised ESR could be subacute so NSAIDs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Bartter Vs gittelman

A

Bartter is usually in childhood with failure to thrive

Also has elevated urinary calcium excretion

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

77 with Colles wrist fracture. Management

A

Start alendronate in patients >= 75 years following a fragility fracture, without waiting for a DEXA scan

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Cause of adrenal insufficiency in developing world

A

TB is most common cause

Remember can get transient low T4 , but corrects with steroid replacement

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

Management of patient that presents with hypoglycemia. BG of T2DM, on metformin and gliclazide

Not responsive to 10% dextrose

What is management

A

Octreotide in sulphonylurea OD
- blocks insulin secretion

(aka Sandostatin - synthetic somatostatin)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Most likely cause of Low TSH levels in hospitalised patients

A

Sick thyroid syndrome 3x more likely than hyperthyroidism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Management of gestational diabetes

A

Fasting >=5.6
2hr glucose >= 7.8

Fasting glucose 5.6 - 7 then diet,+/- Metformin after 1-2/52

6-6.9 with complications -macrosomia or hydramnios, then offer insulin

Fasting >7 then start insulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Management of subclinical hypothyroidism

A

Treat if TSH above 10 (if younger than 70)

TSH 4-10 then treat if symptomatic

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

Hyponatremia with normal osmolarity

A

Pseudohyponatraemia

… serum Na is measured as a ratio of Na to plasma volume. If the patients plasma has high amounts of proteins or lipids, the plasma volume will be increased resulting in a measured hyponatraemia. This is not a true hyponatraemia as the actual ratio of sodium to plasma fluid will be normal.

So look out for hyperproteinaemia (e.g. TPN, IVIG) and hyperlipidaemia (in particular hypertriglyceridemia)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Management for patient with familial hypercholesterolemia

A

First line: high dose statins.

Second line: Ezetimibe (inhibits the intestinal absorption of cholesterol)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Calcium in adrenal Insufficiency

A

hypercalcemia—
combination of increased calcium input into the extracellular space and reduced calcium removal by the kidney

hyponatraemia in 85–90%
hyperkalaemia in 60–65%,
“hypercalcaemia is a rare occurrence”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

familial benign hypocalciuric hypercalcaemia Vs primary hyperparathyroidism

A

Both may have high calcium with high or (inappropriately) normal PTH

But FHH has low urinary calcium
High calcium should lead to high urinary calcium

FHH is auto dom asymp hypercal - defect in the calcium-sensing receptor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is familial benign hypocalciuric hypercalcaemia

A

FHH is auto dom asymp hypercal - defect in the calcium-sensing receptor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

macroadenoma with high prolactin management

A

If prolactin extremely high (>6000) then prolactinoma, so treat with bromocriptine or cabergoline (dopamine-R agonist)

In macroadenoma, other may be reduced and prolactin can be raised ( 600–3000 mU/L) secondary to pit stalk blockage w prevention of dopamine reaching the pituitary
Mx Trans-sphenoidal surgery

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

Management of insulinoma

A

CT scan - 10% are malignant 10% are multiple
50% are MEN1
Refer to surgery
Diazoxide and somatostatin are tx options if not surgery

22
Q

52y w galactorrhoea. Generally fatigued. Prolactin 440, what is next test?

A

Pregnancy, TFTs (hypothy common cause)

MRI if these ruled out

23
Q

Management of hyperparathyroidism

A

Total parathyroidectomy

Conservative if calcium less than 0.25 above AND under 50y AND not symptomatic (fragility#, renal stones) AND eGFR over 60

Can use calcimemetics like cinacalcet

24
Q

Hypokal differentials

A

CCL (Cushing’s Conn’s liddle) hypertension
Gitelman gentleman (older but still only 20s), decreased Ca urine
Bart has a Cat (bart is also child)
Liddle you get when you’re little

25
Diagnosis of growth hormone deficiency
First line: IGF-1 may be raised (but N in 30-40%) If unsure: oral glucose tolerance test (OGTT) with serial GH measurements (normally would get suppressed to <2 in hypergly) Contraindicated w IHD or seizures so use arginine-GHRH simulation test
26
Management of acute thyrotoxicosis
IV propranolol Propylthiouracil or Methimazole Lugol's iodine Dexamethasone (blocks T4 to T3 conversion Stop aspirin as it can worsen storm by displacing T4 from thyroid binding globulin
27
Markers of severe DKA
``` pH <7 Blood ketones >6 Bicarb <5 Anon gap >16 K <3.5 on admission Tachy or Bradycardia Sys BP <90 O2<92 GCS<12 ```
28
Myxedema coma management
Combo of levo and liothyronine Fluid resus Not great evidence for T3 because of lack of RCT but T3 has faster onset
29
Pregnant woman with history of Graves
thyrotrophin (TSH) receptor stimulating antibodies should be checked at 30-36 weeks gestation - helps to determine the risk of neonatal thyroid problems
30
Management of papillary thyroid cancer
Thyroidectomy and radio iodide therapy
31
Progression of Subacute (De Quervain's) thyroiditis
4 phases 1) lasts 3-6/52, hyperthy, painful goitre, raised ESR, decreased uptake 2) 1-3/52 euthy 3) weeks-months hypothy 4) goes back to normal
32
Incidental 3mm thyroid mass found on CT. Asymptomatic
non-palpable nodule found on imaging that are < 1cm don't need biopsy, managed in primary care
33
Signs of congenital adrenal deficiency pneumonic
2 1 def- Low mineralocorticoids - Increased androgens (normal BP - virilizing) 1 7 def- Increased mineralocoticoids- Low androgens (HTN - non virilizing) 1 1 def- Increased mineralocorticoids- Increased androgens (HTN - virilizing)
34
Electrolytes suggestive of laxative abuse
Hypokal with reduced k urinary excretion | Kidneys trying to hold on to it May have calluses on hand from vomiting
35
CK and thyroid disease
CK is modestly elevated (<10x upper limit) in up to 90% of untreated hypothy, and up to 79% complain of muscle symptoms Polymyositis unlikely if <1000
36
Pt has hx of phaeochromocytoma and presents w thyroid swelling. What is the most appropriate next test to confirm the diagnosis?
Calcitonin levels - as could be MEN 2a or b, with a Medullary thyroid cancer parafollicular (C) cells, which secrete calcitonin)
37
classic hx of pseudo-cushings
``` severe psychotic depression or alcohol use mildly raised 24-h urinary free cortisol (unlike 3x upper limit in Cushing's) low dose (1mg) dex ... cortisol 55 nmol/L (<50) ```
38
interpretation of raised dehydroepiandrosterone sulphate in PCOS investigations
DHEA is produced by adrenal cortex | If raised it points to an adrenal rather than an ovarian source, making ovarian tumour unlikely
39
urinary sodium in vol depletion
low urinary sodium (appropriate response to volume depletion)
40
hyperthyroid in pregnancy
propylthiouracil in first trimester then carbimazole
41
post-partum thyroiditis
``` usually hyper (don't treat, maybe propanolol then hypothy (can treat) then euthyroid ```
42
``` severe psychotic depression mildly raised 24-h urinary free cortisol low dose (1mg) dex ... cortisol 55 nmol/L (<50) ```
classic hx of pseudo-cushings often due to alcohol excess or severe depression
43
cause of amenorrhoea in low BMI
hypothalamic amenorrhoea
44
The history of T1DM and coeliac, with a new likely diagnosis of Hashimotos..... probable diagnosis and what test?
Very suggestive of Autoimmune polyendocrinopathy syndrome type 2, which Addisons is strongly linked to treating for Hashmitos which could result in an Addisonian crisis short synacthen test
45
low calcium, high phosphate, high PTH
could be secondary hyperparathyroidism in context of CKD - CKD leads to high phosphate, and low Vit D... causing osteomalacia ``` or pseudohypoparathyroidism, where there is receptor insensitivity to PTH due to G-protein mutation... audo dom short fourth and fifth metacarpals cognitive impairment obesity round face ```
46
pseudohypoparathyroidism types
1a Has a characteristic phenotypic appearance (Albright's hereditary osteodystrophy) Type 1b and 2 no phenotype but has biochem but 2 has normal cAMP response to PTH stimulation
47
pt w low Ca, Mg, and PTH
Magnesium deficiency causes hypocalcaemia Without sufficient levels of magnesium, PTH cannot function properly e.g. due to PPI
48
Secondary hyperparathyroidism vs vit d deficiency/osteomalacia
both low calcium high PTH vit d def usually has low Phosphate too, whereas that's high in secondary hyperpara (CKD leads to low Vit D and high phosphate -reduced excretion) Vit D def /Osteomalacia has raised ALP
49
Low Calcium, Raised ALP
could be osteomalacia - check Vit D esp if phenytoin, Coeliacs, cirrhosis, Type 2 RTA (hypokal)
50
hx of weight loss | Low TSH and T4. Management?
In approximately 5% of patients with clinical and biochemical hyperthyroidism, T3 may be elevated prior to T4. This is known as T3 toxicosis. If TSH and T4 T3 are low then its subclinical thyrotoxicosis
51
Management of secondary hyperparathyroidism
Reduce phosphate in diet - reduction in foods like chocolate, nuts, shellfish and cola Next step is a phosphate binder like Sevelamer or Lanthanum carbonate Vit D replacement alfacalcidol Can have parathyroidectomy
52
Common consequences of acromegaly
T2DM Hypertension LVH, doesn't improve after treatment 33% have sleep apnoea, but tends to improve after treatment 30% have premalig colononic polyps, and 5% develop cancer colonoscopic screening, starting at the age of 40 years