Endocrinology and Metabolic Medicine Flashcards

(40 cards)

1
Q

What are the hypothalamic releasing and inhibiting factors?

A
Releasing:
GnRH
GHRH
TRH
CRH
Inhibiting:
Somatostatin
Dopamine
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2
Q

Which releasing factors act on the anterior pituitary and what do they cause to be released or downregulated?

A

GnRH - LH and FSH which acts on the gonads to produce androgens
GHRH - GH acts on liver to cause growth via Insulin-like GF
TRH - releases TSH, causing the thyroid to release thyroxine
Somatostatin - down-regulates GH and TSH release
Dopamine - down-regulates prolactin release
CRH - ACTH release causes steroid synthesis in the adrenals

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3
Q

What hormones are released by the posterior pituitary

A

vasopressin - renal tubules

oxytocin - breasts and uterus

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4
Q

Symptoms of over-production in the pituitary

A

Acromegaly - prognathism, interdental separation, large tongue, spade-like hands and feet, tight-fitting rings, or gigantism in children
Prolactin excess - galactorrhoea, gynecomastia
ACTH excess - nelson’s (hyperpigmentation, visual disturbance, headaches, menstrual cycle disturbance) or Cushing’s (weight gain, central fat distribution, abdominal striae, hirsutism, mood changes, gonadal dysfunction)

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5
Q

Local effects of pituitary tumours

A

bitemporal hemianopia
cavernous sinus infiltration - III (ptosis, lateral gaze), IV (diplopia corrected with head tilt) and VI (lateral rectus palsy) cranial nerve palsy
Bony or meninges infiltration - headaches
hypothalamus infiltration - obesity, precocious puberty
ventricular infiltration - hydrocephalus

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6
Q

what is the short synACTHen test?

A

ACTH analogue is given, which should stimulate cortisol secretion
measure plasma cortisol should rise to over 500nmol/L
A negative response suggests primary hypoadrenalism (Addison’s)

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7
Q

What is an insulin tolerance test?

2 CIs

A

measures growth hormone response
can assess pituitary reserve
CI IHD and epilepsy

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8
Q

What is a dexamethasone suppression test?

A

dexamethasone should suppress ACTH and cortisol

failure to suppress suggests cortisol excess - Cushing’s

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9
Q

symptoms of hypopituitarism

A
gonadotrophin deficiency:
loss of libido, erectile dysfunction, amenorrhoea
Hyperprolactinaemia:
galactorrhoea, hypogonadism
GH deficiency:
Short stature in children, no effect in adults
Hypothyroidism and adrenal failure:
TATT, weight gain, slow, depression.
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10
Q

Causes of hypothyroidism (5)

A

Primary:
primary atrophic hypothyroidism (common) - no goitre
Hashimoto’s thyroiditis - immune infiltrate causes goitre
Iodine deficiency - rare in UK due to water supplementation
Iatrogenic - surgery, radioiodine treatment, amiodarone, lithium, iodine
postpartum or De Quervain’s thyroiditis - painful goitre
Secondary: v rare due to hypopituitarism

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11
Q

Causes of hyperthyroidism (6)

A

Graves - common, immune infliltrate causes goitre
toxic multinodular goitre - older, iodine deficient patients. decompressive surgery.
toxic adenoma - solitary overactive nodule
ectopic thyroid tissue - Metastatic thyroid cancer or teratoma
iodine or thyroxine excess
thyroiditis - postpartum, due to amiodarone

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12
Q

ECG changes in myoxoedemic crisis

A

heart block, prolonged QT, ST and T wave changes

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13
Q

adrenal layers and their hormones

A

zona glomerulosa - mineralocorticoids - fluids - Na retention, salivary glands, sweat, colon, BP
Zona fasiculata - glucocorticoids - anti-inflammatory, promote glouconeogenesis, lipolysis and inhbit glucose uptake
Zona reticularis - androgens - secondary to gonads
Adrenal medulla- catecholamines - sympathetic nervous system

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14
Q

Adrenal excess - name and causes (7)

A

cushing’s syndrome
ACTH dependent
-pituitary disease - cushing’s disease
-ectopic ACTH - small call and carcinoid tumours
-ACTH administration
ACTH independent causes
-adrenal adenomas
- adrenal carcinomas
- glucocorticoid administration (MOST COMMON)
Alcohol-induced psuedo-cushing’s syndrome

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15
Q

symptoms of Cushing’s (7)

A
central obesity +/- buffalo hump
plethoric complexion
thin, easily bruising skin
striae on the abdomen, legs, breasts
proximal myopathy
pathological #
hypertension
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16
Q

what is Addison’s disease?

A

adrenal insufficiency due to autoimmune destruction of the adrenal cortex. May also be due to TB, surgical removal of adrenals or malignant infiltration.

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17
Q

Symptoms of Addison’s

A

lethargy, depression, anorexia, weight loss
postural hypotension and salt craving
hyperpigmentation in skin folds
vitiligo and hair loss in women

18
Q

symptoms of Addisonian crisis

A
vomiting
abdominal pain
profound weakness
hypoglycaemia
hypovolaemia
19
Q

management of Addisonian crisis (5)

A
take cortisol and ACTH, calcium and other bloods
give 100mg IB hydrocortisone
give fluids - saline
treat hypoglycaemia 
treat precipitating cause
20
Q

Primary hyperaldosteronism presentation and causes

A

hypertension, hypernatraemia, and hypokalemia
adrenal hyperplasia
adrenal adenoma
adrenal carcinoma (rare)

21
Q

diagnostic criteria for diabetes

A

present once if symptomatic, twice if asymptomatic.
Fasting BM - 6.0 to 7.0 = prediabetse, >7.0= diabetes
HBA1C 41 to 48 = prediabetes, >/=48 = diabetes

22
Q

DKA management

A

Fluids

fixed rate insulin infusion 0.1u/kg/hr and usual long-acting insulin

23
Q

Causes of thyroid storm (4)

A

thyroid or non-thyroidal surgery
trauma
infection
acute iodine load e.g. CT contrast media

24
Q

presentation of thyroid storm (7)

A
fever > 38.5ºC
tachycardia
confusion and agitation
nausea and vomiting
hypertension
heart failure
abnormal liver function/jaundice
25
management of thyroid storm (6)
symptomatic treatment e.g. paracetamol treatment of underlying precipitating event IV propranolol anti-thyroid drugs: e.g. methimazole or propylthiouracil Lugol's iodine dexamethasone - e.g. 4mg IV qds - blocks the conversion of T4 to T3
26
Phaeochromocytoma what is it? associations
``` catecholamine secreting tumour 10% are familial - associated with MEN type II, neurofibromatosis and von Hippel-Lindau syndrome 10% are bilateral 10% are malignant 10% are extra-adrenal ```
27
symptoms of phaeochromocytoma (5)
hypertension | episodic palpitations, anxiety, sweating, headaches
28
diagnostic test for phaeochromocytoma
24hr urinary metanephrines
29
Mx of phaeochromocytoma
surgery is definitive Mx | alpha then beta-blocker to control hypertension until then
30
What is SIADH?
hyponatraemia secondary to excessive water retention
31
causes of SIADH (5 categories)
Brain injury - stroke, SAH, subdural, infection Malignancy- SCLC Infections - TB, pneumonia Drugs - SSRIs, TCAs, carbamazepine, sulfonylureas, vincristine, cyclophosphamide Hypothyroidism
32
Mx of SIADH
slowly replace Na to prevent central pontine myelinolysis Fluid restriction drugs - ADG receptor antagonisits
33
MEN I
Three Ps Parathyroid (95%): hyperparathyroidism due to parathyroid hyperplasia Pituitary (70%) Pancreas (50%): e.g. insulinoma, gastrinoma (leading to recurrent peptic ulceration) Also: adrenal and thyroid Commonly present as hypercalcaemia
34
MEN II
``` Medullary thyroid cancer (70%) 2 P's Parathyroid (60%) Phaeochromocytoma RET Oncogene ```
35
MEN III
Medullary thyroid cancer 1 P Phaeochromocytoma Marfanoid body habitus Neuromas RET Oncogene
36
A second drug should be added in type 2 diabetes mellitus when?
HbA1c is > 58 mmol/mol
37
hypoglycaemia with reduced GCS Mx
give 100ml 20% IV Glucose if there is access
38
What is gastroparesis
GI autonomic neuropathy often due to diabetes erratic blood glucose control, bloating and vomiting management options include metoclopramide, domperidone or erythromycin (prokinetic agents)
39
oral hypoglycaemic choice in T2DM
start with metformin and titrate dose accordingly if not adequeate add a gliptin if obese if not add a sulfonylurea if not (glicazide)
40
ECG changes in hypocalcaemia
Common: Corrected QT interval prolongation Rare: Atrial fibrillation or torsade de pointes