Endocrinology Flashcards

1
Q

What is the most common cause of acromegaly

A

Pituitary macroadenoma

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2
Q

Most common complaints of acromegaly patient

A

headache and sweating

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3
Q

cause of excessive sweating in acromegaly

A

sweat gland hypertrophy

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4
Q

Cause of headache in acromegaly

A

compression of diaphragmatica sella

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5
Q

Clinical features of acromegaly

A

1) Headache
2) Increased sweating
3)Skull growth : prominent supraorbital ridge with large frontal sinuses
4)Enlargement of lips,nose,tongue
5)Prognathism
6)Enlargement of hands and feet (spade like)
7)Hypertension, Cardiomyopathy

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6
Q

1st line investigation for acromegaly?

A

serum IGF-1 level

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7
Q

Diagnostic test of acromegaly?

A

OGTT followed by serial measurements of GH and IGF-1 levels

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8
Q

acromegaly patients should be screened for which malignancy

A

Colonic cancer

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9
Q

acromegaly associated with which endocrine syndrome

A

MEN-1

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10
Q

Treatment of choice in acromegaly

A

trans-sphenoidal surgery

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11
Q

2nd line treatment of acromegaly

A

medical treatment

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12
Q

which medical treatment is used prior to surgery in acromegaly

A

Somatostatin analogues because they shrink tumor size

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13
Q

types of medical management in acromegaly

A

1) Somatostatin analogues-Octreotide,Lanreotide,Pasireotide

2) Dopamine Agonists-Bromocriptine,Cabergoline

3)GH receptor antagonist-Pegvisomant

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14
Q

Mechanism of action of Pegvisomant

A

GH receptor antagonist

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15
Q

Causes of Hypercalcemia:

A

Hypercalcemia with N/High PTH:
1) Primary or tertiary hyperparathyroidism
2) Lithium induced hyperparathyroidism
3) FHH
Hypercalcemia with low PTH:
1) Malignancy ( lungs,breasts,myeloma,kidney,lymphoma,thyroid)
2) Elevated vit D ( D intoxication, sarcoidosis, HIV, other granulomatous diseases)
3)Thyrotoxicosis
4)Paget’s disease with immobilisation
5)Milk Alkali Syndrome
6)Thiazide Diuretics
7)Glucocorticoid Deficiency

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16
Q

Most common cause of Hypercalcemia with N/High parathyroid levels:

A

Primary hyperparathyroidism

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17
Q

Most common cause of hypercalcemia with low PTH level:

A

Malignant hypercalcemia

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18
Q

Hypercalcemia+ high phosphate level+ raised ALP in renal impairment =

A

Tertiary hyperparathyroidsm

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19
Q

Cause of Hypercalcemia in malignancy

A

PTH related peptide

20
Q

How to differentiate between FHH and primary hyperparathyroidism-

A

24 hr urinary calcium levels

21
Q

Causes of hypocalcemia:

A

1) Hypoalbuminemia
2)Alkalosis
3)Vitamin D deficiency
4)Chronic renal disease
5)Hypoparathyroidsm
6)Pseudohypoparathyroidsm
7)Acute Pancreatitis
8)Hypomagnesaemia

22
Q

Most common cause of hypocalcemia:

A

Hypoalbuminemia

23
Q

Which is more specific to detect latent tetany?

A

Trousseau’s sign

24
Q

ECG features of hypocalcemia:

A

-Prolonged QT interval
-Ventricular arrhythmia

25
Q

Hypocalcemia+ hypophosphataemia+ bone pain and fracture=

A

Vitamin D deficiency

26
Q

Management of severe hypocalcemia:

A

-10-20 ml 10% calcium gluconate I/V over 10-20 minutes with cardiac monitoring

27
Q

Most common cause of primary hyperparathyroidsm:

A

Single parathyroid adenoma

28
Q

Hypocalcemia with hypomagnesemia. Which one needs correction first?

A

hypomagnesemia. Because low mg levels cause hypocalcemia.
Rx: 50 mmol (1.23g) I/V magnesium chloride over 24 hours

29
Q

Treatment of choice for primary hyperparathyroidsm:

A

Surgical excision of adenoma

30
Q

Causes of secondary hyperparathyroidism:

A

1)Chronic kidney disease
2)Malabsorption
3)Vitamin D Deficiency (Osteomalacia and rickets)

31
Q

Indication of surgery for primary hyperparathyroidsm:

A

1) Individuals with clear cut symptoms: renal stones, renal impairment,osteoporosis
2)Asymptomatic patients with significant hypercalcemia ( >11.4 mg/dl or corrected level >2.85 mmol/l)

32
Q

Treatment of tertiary hyperparathyroidism-

A

Cinacalcet

33
Q

Mechanism of action of Cinacalcet:

A

Enhances the sensitivity of the calcium sensing receptor which reduces PTH levels

34
Q

2nd line Rx for primary hyperparathyroidsm-

A

Cinacalcet

35
Q

which type of genetic disorder is FHH?

A

Autosomal dominant

36
Q

Pathogenesis of FHH:

A

“Inactivating” mutation in calcium sensing receptor gene

37
Q

Level of Hypercalcemia in FHH?

A

Mild

38
Q

Most common cause of hypoparathyroidsm-

A

Damage to parathyroid glands during surgery

39
Q

Mirror image of FHH:

A

Autosomal dominant Hypoparathyroidsm ( due to activating mutation in calcium sensing receptor gene)

40
Q

Pseudohypoparathyroidsm:

A

Tissue resistance to PTH

41
Q

PTH levels in Pseudohypoparathyroidsm:

A

Markedly elevated

42
Q

In Pseudohypoparathyroidsm mutations occur in which gene?

A

GNAS1

43
Q

A short stature, round face obese patient. Lab shows hypocalcemia and hyperphosphatemia. You notice short 4th metacarpal and metatarsals. Dx?

A

Albright’s hereditary Osteodystrophy / Type 1a Pseudohypoparathyroidsm

44
Q

Pseudohypoparathyroidsm:
mutation involves-

A

Maternal gene

45
Q

pseudopseudohypoparathyroidsm: mutation involves-

A

Paternal gene

46
Q

pseudopseudohypoparathyroidsm

A

Clinical features of AHO but normal serum calcium and PTH levels