Chempath Flashcards
Distinguish between HONK and DKA
Anion gap (ketones in DKA increase anion gap)
Thyroid cancers
- Medullary
- Papillary
- Follicular
- Anaplasitc
Features
- MEN2, Calcitonin, Parafrollicular “C” cells
- Psammoma bodies
- Nodules and mets
- Elderly
Rate limiting haem synthesis
AminoLenvulinic Acid synthase
Deficiency of this –> high urea
Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)
in e.g. Lesch Nyhan Syndrome
Hyperuricaemia, Gout, PRT (Prutt)
Gynaecomastia + wants viagra
Prolactinoma (prolactin will be >6000)
Rounded mass with glands and mucin in Liver
Met from pancreatic adenocarcinoma
Histology of acute fatty liver hep
Ballooned cells, mallory denk bodies, neutrophils
Alcoholic hepatitis with fibrosis histology
Ballooned cells, mallory denk bodies, MEGAMITOCHONDRIA, pericentricular fibrosis
Alpha Fetoprotein raised in?
Hepatocellular Carcinoma, pregnancy, testicular Ca
What type of Br can be seen in urine?
Unconjugated only (e.g. haemolysis)
High Br, high ALP, high GGT
Could be drug induced cholestasis
Corrected calcium
measured + 0.02(40-albumin)
Baby with seizures, low Ca, low PTH
Primary hypoparathyroidism in e.g. Di George
Low mood after renal transplant for longstnading renal disease (high Ca, high PTH)
Tertiary hyperparathyroidism
B12 vs folate deficiency
B12: glossitis, jaundice, dementia, other AI conditions, vegans
Folate: diarrhoea, methotrexate
IBD can cause either (methotrexate->folate, loss of terminal ileum absorption->B12)
Vitamins B1 B2 B3 (Niacin) B6
B1 - Wernicke’s encephalopathy/Korsakov Syndrome/beri beri –> cardio/neuro (RBC transketeolase)
B2 - Riboflavin (glossitis, RBC glutanthione reductase)
B3 Niacin - Pellagra - dementia, diarrhoea, dermatitis
B6 - Pyridoxine (dermatitis, anaemia, neuropathy)
What does Denosumab target?
RANK-L on Osteoclasts (inhibit) for osteoporosis or bony mets
Allopurinol interacts with
Azathioprine
Acute intermittent porphyria Ix
Urine porphobilinogen (and Urine Aminolevulinic Acid)
In guthrie how do you measure
Hypothyroid
CF
MCADD
TSH
Immunoreactive trypsinogen
Acylcarnitine
Normal anion gap
18mM
Primary hyperparathyroidism Vit D levels
Vit D is low as it is consumed
High Ca + haematuria
Renal stone
Band keropathy
Long term hyperCa
Addisons + primary hypothyroidism + diabetes
Schmidt syndrome (AIPS2)
HTN + Adrenal mass (3 causes)
Phaeo, Conns, Cushings
High functioning adrenal (3 causes)
Cushings, Conns, CAH
Low functioning adrenal
Sepsis, haemorrhage, discontinuation of steroids, Addisons
MI Markers
Troponin - rises within 4-6 hours, peaks 12-24 hours, remains high for 3-10 days
CK - rises withing 24 hours (check if double MI)
Myoglobin rises quickly
MEN 1
Pituitary, Pancreas, Parathyroid
MEN 2a
Parathyroid, Phaeo, Thyroid (med)
Men 2b
Phaeo, Thygoid, Ganglioneuroma
Tertiary hyperparathyroidism
Often in people with CKD
Longstanding 2° hyperparathyroidism –> gland hyperplasia –> permanent dysregulated high secretions of TSH –> 1° hyperparathyroidism picture
End result: High PTH, high Calcium, variable PO4 levels
T1DM has low Na, everything else is normal. Diagnosis?
hyperlipidaemia
High K, low Na, urine osmolality >20
CKD/Renin (RAS) cause not aldosterone
Urine osmolality > plasma osmolality
SIADH
Low K, alkalosis, hypotension, hypercalciuria
Bartter Syndrome
DELETE
Low K and acidosis
Renal tubular acidosis
Non-alcoholic fatty liver disease LFTs
High ALT and AST ratio 1:1
High GGT
Normal Br and Alb
Low caeruloplasmin
Wilsons
Vitamin C deficiency affects what thing to cause bleeding gums and poor dentition?
Collagen
Vit E deficiency
Haemolytic anaemia, areflexia, ataxia
Vit B6 deficiency
AKA Pyroxidine
Dermatitis, peripheral neuropathy, sideroblastic anaemia
Can be caused by isoniazid
Fair skin, brittle hair, developmental delay, intellectual disability
Homocystinuria
Glucose-6-phosphate dehydrogenase, hypoglycaemia, big kidneys and liver
von Gierke’s syndrome
Toxic encephalopathy causing poor feeding, hypotonia and seizures
Sweet odour and sweaty feet
Maple Syrup Urine disease
Cherry-red spot and dymorphia
LYsosomal storage disorder (e.g. Fabry’s)
Phenytoin toxicity
ataxia and low BP
Lithium SEs
tremor and thirst
Gentamicin toxicity
Ears and kidneys
Tinnitus - ringing in ear
Gentleman caller ringing
Low vit D, low Ca, high PTH
Osteomalacia (not 2° hyperparathyroidism as vit D is the causative problem)
Chronic renal failute, high Ca, high PTH
3° hyperparathyroid
Thiamine (B1) test
Red cell trasketolase activity
Floppy neonate not feeding
Cataract and conjugated jaundice post milk feed
Galactosaemia
Why do you give Calcium gluconate in hyperkalaemia
As it is cardioprotective and helps prevent fatal dyrhythmia (does not lower K)
CKMB is useful for what in heart medicine
detecting re-infarction as levels rapidly return to normal so would know if was a second one
In an SIADH picture what must you exclude before diagnosing SIADH?
Drugs causing it
- Causes of pseudo-hyponatraemia
2. what will the osmolality be doing?
- High lipids or proteins or a spurious sample
- The osmolality will be normal (low in true hyponatraemia)
It is caused by dilution
High PTH but high PO4 and low Ca
Pseudohyperparathyroidism (Martin-Albright Syndrome)
Generic resistance to PTH
High PTH but Ca and PO4 respond as if low PTH
Anion gap MUDPILES (or KULT)
Metformin *Uraemia *DKA (Ketones) Paraldehyde Iron *Lactic acid Ethanol/methanol Salicylates
- Are KUL
Non* are all the Toxins
Low sodium, all else (K+, CL-?) normal. Glucose before OGTT is 4.9, 2 hours later is 10 ish. Diagnosis?
Impaired Glucose Tolerance
A teenager presents with a history of several weeks of increased thirst (polydipsia), increased urination (polyuria) / High urinary output and weight loss - diagnosis?
Type 1 diabetes mellitus