interactive haem, endo, renal and rheum cases Flashcards

1
Q

what macrolide is given for atypical pneumonia

A

clarithromycin or erythromycin

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2
Q

atypical pneumonia organisms

A

mycoplasma pneumoniae, chlamydia pneumoniae, legionella pneumophila

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3
Q

how is microcytic anaemia diagnosis confirmed

A

coeliac screen and confirm diagnosis on duodenal biopsy which shows villous atrophy

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4
Q

how is microcytic anaemia investigated

A

ogd and colonoscopy depending on upper/lower gi symptoms

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5
Q

causes of bloody diarrhoea

A

infection - infective colitis
inflammation - ulcerative/crohns colitis (young)
ischaemia - ischaemic colitis (older)
malignancy (more likely to be constipation), diverticulitis

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6
Q

what is caput medusa

A

direction of flow in the veins below the umbilicus is towards the legs

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7
Q

what can portal hypertension cause

A

encephalopathy, ascites, spontaneous bacterial peritonitis, variceal bleed

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8
Q

what signs indicate haemolytic uraemic syndrome (HUS)

A
low haemoglobin and high bilirubin (due to haemolysis).
high urea and creatinine (uraemia). 
low platelets
diarrhoea
schistocytes - red cell fragments
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9
Q

how to recognise immediate transfusion reaction due to haemolysis

A

fever, rigor, increase pulse rate, decreased bp, chest pain, dark urine (conjugated bilirubin)

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10
Q

what three things can microangiopathic haemolytic anaemia be caused by

A

DIC (disseminaed intravascular coagulation), HUS (haemolytic uraemic syndrome), TTP (thrombotic thrombocytopenic purpura)

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11
Q

what are the signs of DIC

A

low platelets and fibronogen (used to make clots)
high PT/APTT (due to low clotting factors n platelets)
high D-dimer/fibrin degradation products (due to increased fibrinolysis

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12
Q

what are the signs of TTP (thrombotic thrombocytopenic purpura)

A

HUS + fever + neurological manifestations (headaches)

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13
Q

causes of hereditary haemolytic anaemia

A
  • Defects of RBC membrane production (hereditary spherocytosis)
  • Haemoglobinopathy (sickle-cell disease, thalassaemia)
  • Defective RBC metabolism (G6PD deficiency, PK deficiency)
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14
Q

causes of acquired haemolytic anaemia

A

autoimmune
drugs
infection
maha (microangiopathic haemolytic anaemia)

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15
Q

anaemia signs and symptoms

A

fatigue, breathlessness on walking, pallor, conjunctival pallor, koilonychia, tachycardia, soft systolic murmur- flow murmur

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16
Q

what can polycythaemia be secondary to

A

chronic hypoxia in chronic lung disease, high altititude, renal cell tumours secreting EPO

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17
Q

what blood markers increase in bacterial and viral infections

A

bacterial - neutrophils

viral - lymphocytes

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18
Q

what are the features of hypovolaemia

A

postural hypotension, tachycardia, reduced skin turgor, dry mucous membranes

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19
Q

if the pt is hypovalaemia, what are the causes of their hyponatraemia

A

diarrhoea, vomiting, diuretics and salt losing nephropathy

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20
Q

if the pt. is euvolaemic, what is the cause of their hyponatraemia

A

hypothyroidism, adrenal insufficiency, SIADH

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21
Q

ix of hypovolaemia

A

low urine sodium

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22
Q

ix of euvolaemia

A

tfts - hypothyroidism
short syncacthen trst - adrenal insufficiency
plasma and urine osmolality

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23
Q

if the pt is hypervolaemia, what is the cause of their hyponatraemia

A

cardiac failure
cirrhosis
nephrotic syndrome

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24
Q

ix of hypervolaemia

A

fluid oveloaded, low urine sodium

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25
how does hypokalaemia present
weakness arrhythmia polyuria
26
what are the ddx of hypokalaemia
vomiting diuretics primary hyperaldosteronism - bilateral hyperplasia or conns tumour
27
what are almost all cases of hyponatraemia due to
too much ADH
28
what are some rarer causes of hyponatraemia
excess water intake sodium free irrigation solutions(e.g glycine solution used in TURP --> post op - pt may wake up confused due to low na as they have absorbed the irrigation fluid)
29
causes of siadh
cns pathology - haemotoma, stroke, tumour lung pathology - pneumonia, cancer drugs - ssri, ppi, opiates tumours
30
causes of onycholysis
trauma, thyrotoxicosis, fungal infection, psoriasis
31
sweating, weight loss n onycholysis diagnosis
thyrotoxicosis
32
case: abdo pain, vomiting, t1dm, cbg:20, venous ph:7.20. What is the most appropriate next step
capillary ketone (DKA)
33
microvascular complications of diabetes
microvascular, retinopathy, nephropathy (foot ulcers)
34
macrovascular complications of diabetes
mi,stroke,pvd
35
metabolic complications of diabetes
dka, hhs, hypoglycaemia
36
distinguishing bt small bowel and large bowel on axr
small bowel - valvulae conniventes (folds go all the way across the lumen) large bowel - haustra (semi-lunar folds; dont go all the way across lumen)
37
what are digoxin and metoprolol used for
to rate control for chronic persistent af/>48hr
38
how to rate control <48h af
dc cardioversion
39
how to rate control <48h af
dc cardioversion
40
what is troussseaus sign caused by
low calcium, thrombophlebitis migrans (sign of malignancy - pancreatic or gastric cancer)
41
what is virchows node
a lymph node in left supraclavicular fossa
42
what is caput medusae caused by
porto-systemic shunting in portal hypertension
43
what is troisiers sign
the finding of a hard left supraclavicular node (sign of intra-abdominal malignancy - gastric)
44
when does grey turners sign occur
in pancreatitis, aortic rupture and ectopic pregnancy
45
what is microangiopathic haemolytic anaemia
fibrin deposition in vessels which fragment the blood cells as they pass -i.e haemolysis in small vessels due to clots
46
what is haemolytic uraemic syndrome
endothelial damage triggers thrombosis, platelet consumption and fibrin strand deposition, mainly in renal vasculature
47
case: confused, cough no postural hypotension, low na, high urine osmolality What test do u request next
CXR
48
what are the signs of hypervolaemia
raised jvp and oedema
49
above what urine osmolality is ADH inappropriate
100
50
what is nail pitting caused by
psoriasis, connective tissue disorders, sarcoidosis
51
what is koilnycha caused by
iron deficiency anaemia
52
what is leukonychia caused by
low albumin
53
what are beau's lines and what causes them
arrested nail growth because of severe illness, chemo
54
how are fool ulcers ix n tx
swabs taken, eradicate infection, reduce weight bearing, look at vascular supply
55
global st elevation ddx
pericarditis
56
case: loin pain, normal crp and blood in urine. | What ix do u request
non contrast CT (KUB) - to visualise stones
57
what is primary hyperparathyroidism
high pth drives high calcium, tumour secreting pth
58
what is secondary hyperparathyroidism
pth is high because of low calcium. vit d deficiency or renal failure
59
when u see hypercalcaemia what is the next test to look at
pth
60
causes of hypercalcaemia if pth is high
hyperparathyroidism
61
causes of hypercalcaemia if pth is low
malignancy, inflammatory
62
what are the sources of alkaline phosphatase
liver n bone
63
when is alp increased
in obstructive liver disease and bone disease (malignancy, fracture, pagets disease i.e inc bone turnover)
64
signs n symptoms of bone metastases
backache, high calcium and high alp
65
what cells make alp
osteoblasts
66
why is alp normal in myeloma
plasma cells suppress osteoblasts and activate osteoclasts
67
multiple myeloma acronym
``` CRAB calcium is up renal impairment anaemia bone pain n osteoporosis ```
68
case: young woman w a smooth mobile 1cm lump. what is the most likely ddx
fibroadenoma
69
causes of cavitating lung lesions
infection - tb, staph, klebsiella (alcoholics) inflammation (rhematoid arthritis) infarction - pe malignancy
70
ankle oedema causes
heart failure or low albumin (nephrotic syndrome)
71
case: ankle oedema, normal u+es, normal alt, ast, alp, low albumin, normal echo/ What test dy do next
urinalysis
72
what is nephrotic syndromw
increased permeability of the glomerular basement membrane to protein. proteinura >3g/day. hypoalbuminaemia oedema
73
nephritic syndrome signs
haematuria, hypertension, proteinuria (oedema)
74
what is hereditary haemorrhagic telangiacstasia
autosomal dominant. abnormal blood vessels in skin, mucous membranes, lungs, liver, brain nose bleeds n gi bleeds
75
how to manage hyperglycaemia
``` diet n exercise metformin if overweight sulphonylureas if not overweight insulin sensitisers insulin glp1 analogues gliptins (dpp4 inhibitor ```
76
signs n symptoms of addisons disease/ adrenal insufficiency
low na, high k, short synacthen test | pigmentation and postural hypotension
77
signs of prolactinoma
high prolactin --> low lh n fsh --> low testosterone
78
signsof acromegaly
tumour secreting prolactin and growth hormone (high prolactin n gh) high growth hormone --> high igf -1 production in the liver failure of gh suppression in ogtt
79
signs of premature ovarian failure
low oestrogen and high lh and fsh (due to reduced negative feedback)
80
signs of hypothyoridism
low t3/t4 and high tsh | high prolactin as its stimulated by high levels of trh
81
what is toxic multinodular goitre
when nodules start making excess thyroxine
82
what is conns syndrome (primary hyperaldosteronism)
high na low k - metabolic alkalosis hypertension treat w spironolacctone
83
6 endocrine causes of hypertension
phaeochromocytoma, cushings, conns, acromegaly, renal artery stenosis, co-arctation of the aorta