General Questions Flashcards
HLA-A3
Haemochromatosis
HLA-B5
Behcet’s Syndrome
HLA-B27
Ankylosing Spondylitis,
Reiter’s syndrome,
acute anterior uveitis
HLA-DQ2/DQ8
Coeliac disease
HLA-DR2
Narcolepsy,
Goodpasture Syndrome
HLA-DR3
Dermatitis Herpetiformis
Sjogren’s syndrome
primary biliary cirrhosis
HLA-DR4
Rheumatoid Arthritis,
T1DM (this is also associated less strongly with HLA-DR3)
Cytotoxic MoA + main SFx: cyclophosphamide
MoA: Alkylating agent vs DNA crosslinks
SFx: haemorrhagic cystitis
Cytotoxic MoA + main SFx: Bleomycin
MoA: DNA degradation
SFx: lung fibrosis
Cytotoxic MoA + main SFx: Doxorubicin
MoA: inhibit DNA synthesis
SFx: cardiomyopathy
Cytotoxic MoA + main SFx: Methotrexate
MoA: DHR folate synthesis inhibitor
SFx: fibrosis (lung + liver); myelosuppression
Cytotoxic MoA + main SFx: 5-FU
MoA: thymidylate synthase inhibitor
SFx: dermatitis/mucositis
Cytotoxic MoA + main SFx: 6-mercaptopurine
MoA: Inhibits purine synthesis
SFx: myelosuppression
Cytotoxic MoA + main SFx: Cytarabine
MoA: inhibits DNA polymerase
SFx: myelosuppresion, ataxia
Cytotoxic MoA + main SFx: Vincristine
MoA: MT formation inhibitor
SFx: peripheral neuropathy
Cytotoxic MoA + main SFx: Docletaxel
MoA: inhibits MT depolymerisation
SFx: neutropenia
Cytotoxic MoA + main SFx: Cisplatin
MoA: DNA crosslinking
SFx: ototoxicity
Cytotoxic MoA + main SFx: Hydroxyurea
MoA: reduces DNA synthesis
SFx: myelosuppression
Normal anion gap
10-18 mmol/L
Raised anion gap causes:
Lactate: shock, hypoxia
Ketones: diabetic ketoacidosis, alcohol
Urate: renal failure
Acid poisoning: salicylates, methanol
First line treatment for ethylene glycol poisoning
Fomepizole = alcohol dehydrogenase inhibitor
Ethanol replaced
Haemodialysis for refractory cases
Which is associated with hypokalemia and hypertension: Bartter’s syndrome or Liddle syndrome?
Liddle syndrome
Bartter and Gitelman’s = hypokalemia without hypertension
Antibiotic vs animal bite
Coamoxiclav
Doxy + metro if pen allergic
Name the pathogen:
cutaneous Leishmaniasis -
mucocutaneous Leishmaniasis -
visceral Leishmaniasis -
Cutaneous = L tropica; L mexicana Mucocutaenous = L braziliensis Visceral = L donovani
Antibiotic treatment in bacterial meningitis for those penicillin or cephalosporin allergic?
Chloramphenicol
Klinefelter’s syndrome
Klinefelter’s syndrome is associated with karyotype 47, XXY
Features: often taller than average lack of secondary sexual characteristics small, firm testes infertile gynaecomastia - increased incidence of breast cancer elevated gonadotrophin levels
T9:22
Chronic myeloid leukaemia - 9 ABL (oncogene - an aberrant tyrosine kinase) + 22 B cell receptor
T15:17
Acute pro-myelocytic leukaemia - 15 Promyelocytic gene + 17 Retinoid acid receptor alpha (Fusion protein binds retinoid acid receptor and promotes transcription).
T8:14
Burkitt’s Lymphoma - 8 c-myc (oncogene) + 14 Ig heavy constant region
T14:18
Follicular Lymphoma - 14 Ig heavy constant region + 18 Bcl2 (anti-apoptotic gene)
T11:14
- Mantle Cell Lymphoma 11 - Cyclin D (oncogene) + 14 Ig heavy constant region
Anti-Hu
associated with small cell lung carcinoma and neuroblastomas
sensory neuropathy - may be painful
cerebellar syndrome
encephalomyelitis
Anti-Yo
associated with ovarian and breast cancer
cerebellar syndrome
Anti-GAD antibody
associated with breast, colorectal and small cell lung carcinoma
stiff person’s syndrome or diffuse hypertonia
Anti-Ri
associated with breast and small cell lung carcinoma
ocular opsoclonus-myoclonus
pH threshold for NIV and invasive ventilation in COPD
NIV = 7.25-7.35
Invasive <7.25
Sarcoidosis: poor prognosis
insidious onset, symptoms > 6 months absence of erythema nodosum extrapulmonary manifestations: e.g. lupus pernio, splenomegaly CXR: stage III-IV features black people
Pathogen most commonly causing IECOPD
Haemophilus influenzae
TIA stratification
ABCD2 score Age >= 60 (1) BP >= 140/90 (1) Clinical features: Speech only (1), unilateral weakness (2) D1: Duration <1hr (1) >1hr (2) D2: DM (1)
Score >=4 = high risk –> aspirin 300mg + specialist r/v in 24h
ECG changes in pericarditis
Widespread ‘saddle-shaped’ ST elevation
PR depression = most specific
Epsilon wave on ECG
Diagnostic for Arrhythmogenic Right Ventricular Cardiomyopathy (ARVD).
Is a positive blip following the QRS complex
Hereditary angioedema
C1-INH deficiency. Uncontrolled release of bradykinin.
Leiner Disease
C5 deficiency. recurrent diarrhoea, wasting and seborrhoeic dermatitis
Metformin Sfx
GI upset - 20%
vitamin B12 malabsorption
Lactic acidosis
If neovascularisation is present in macular degeneration what is the investigation of choice?
Fluorescein angiography
Lesion location: upbeat nystagmus
Cerebellar vermis lesion
Downbeat nystagmus cause
Foramen Magnum lesion: Arnold-Chiari malformation
Cluster headache management
Management
acute: 100% oxygen, subcutaneous or a nasal triptan
prophylaxis: verapamil, prednisolone
NICE recommend seeking specialist advice from a neurologist if a patient develops cluster headaches with respect to neuroimaging
Gitelman syndrome
Gitelman’s syndrome is due to a defect in the thiazide-sensitive Na+ Cl- transporter in the distal convoluted tubule.
Features hypokalaemia hypomagnesaemia hypocalciuria metabolic alkalosis normotension
Homonymous hemianopia: incongruous vs congruous
incongruous defects = optic tract lesion; congruous defects = optic radiation lesion or occipital cortex
Mixed Beta and alpha blockers
Carvedilol; labetalol
Actinic keratoses treatment
topical fluorouracil cream
topical steroids/imiquimod
Trastuzumab SFz
Cardiotoxicity - so do an echo before starting
Leptospirosis treatment
penicllin or doxy
Listeria meningitis treatment
IV ampicillin/amoxicillin + gentamicin
Cephalosporins not adequate
Homocystinuria treatment
vitamin B6 (pyridoxine)
new onset RA Rx
Methotrexate + another DMARD + short-course steroids(+ contraception if child-bearing age)
Leprosy antibiotic treatment
Triple therapy: dapsone + rifampicin + clofazimine
Miller-Fisher syndrome triad
Opthalmoplegia + areflexia + ataxia
Is coal dust inhalation linked to lung cancer?
No
Dabigatran reversal
Praxbind = Idarucizumab