Endocrinology Flashcards
(41 cards)
characteristic cutaneous signs of thyrotoxicosis
hair loss
pretibial myxoedema
onycholysis
bulging eyes (exophthalmos/proptosis)
characteristic cutaneous signs of hyothyroidism
hair loss
eyebrow loss outer part
cold, pale skin
characteristic face
characteristic cutaneous signs of cushing’s syndrome
central obesity wasted limbs ('lemon on sticks') moon face buffalo hump supraclavicular fat pads striae
characteristic cutaneous signs of addisons disease
hyperpigmentation (face, neck, palmar creases, mouth)
characteristic cutaneous signs of acromegaly
acral (distal) and soft tissue overgrowth
big jaws (macrognathia), hands and feet
skin is thick
facial features are coarse
characteristic cutaneous signs of hyperandrogenism (females)
hirsutism
temporal balding
acne
characteristic cutaneous signs of hypopituitarism
pale or yellow tinged thinned skin
fine wrinkling around eyes and mouth
characteristic cutaneous signs of pseudohypoparathyroidism
short stature
short neck
short 4th and 5th metacarpals
characteristic cutaneous signs of hypoparathyroidism
dry, scale, puffy skin
brittle nails
coarse hair
microvascular complications of hyperglycaemia
retinopathy
nephropathy
neuropathy
macrovascular complications of hyperglycaemia
stroke
renovascular disease
limb ischaemia
heart disease
symptoms of hyperglycaemia (DM)
polyuria polydipsia unexplained weight loss visual blurring genital thrush lethargy
diagnosis of DM if symptomatic
fasting BM ≥7 OR
random BM ≥11.1
(only one reading required if symptomatic)
HbA1c ≥48 (6.5%)
diagnosis of DM if asymptomatic
fasting BM ≥7 OR
random BM ≥11.1 OR
OGTT 2h value ≥11.1
(need 2 readings if asymptomatic)
HbA1c ≥48 (6.5%)
what is type 1 DM
Insulin deficiency from AUTOIMMUNE DESTRUCTION of insulin-secreting pancreatic beta-cells
Patients must have insulin, and are prone to ketoacidosis and weight loss
what is LADA
o Latent autoimmune diabetes of adults (LADA) is a form of type 1 DM, with slower progression to insulin dependence in later life.
usually have glutamic acid decarboxylase autoantibodies (GADA).
what is type 2 DM
Reduced insulin secretion ± increased insulin resistance
Associated with obesity, lack of exercise, calorie and alcohol excess
≥80% concordance in identical twins, indicating STRONGER GENETIC INFLUENCE THAN IN TYPE 1 DM.
o Typically progresses from a preliminary phase of impaired glucose tolerance or impaired fasting glucose.
what is MODY
Maturity onset diabetes of the young (MODY) is a rare autosomal dominant form of type 2 DM affecting young people with a positive family history.
what is impaired glucose tolerance
known as pre-diabetes.
- Fasting plasma glucose <7mmol/l and OGTT 2h glucose ≥7.8mmol/l but ≤11.1mmol/l
OGTT is not used routinely now – this has been replaced by HbA1c which indicates that a HbA1c of 42-47 (6-6.4%) indicates pre-diabetes and therefore a high risk of diabetes.
what is impaired fasting glucose
- Fasting plasma glucose between 6.1 and 6.9 mmol/L and;
- A blood glucose of <7.8 mmol/L after a 2h OGTT
which factors increase your risk of IGT or IFT
overweight/obese FHx of diabetes sedentary lifestyle hypertension high cholesterol gestational diabetes
secondary causes of DM
steroids, anti-HIV drugs, atypical antipsychotics, thiazides
Pancreatic - pancreatitis, surgery (>90% pancreas removed), trauma, pancreatic destruction (haemochromatosis, CF), pancreatic cancer.
cushing's disease acromegaly phaeochromocytoma hyperthyroidism pregnancy
complications of gestational diabetes
miscarriage pre-eclampsia macrosomia shoulder dystocia pre-term labour congenital malformations worsening of diabetic complications e.g. retinopathy, nephropathy.
who is at risk of gestational diabetes
age >25y FHx positive weight gain non-caucasian HIV positive previous gestational DM