Difficult Topics 2 Flashcards

1
Q

Non-healing ulcer, with hard, raised everted edges

A

Squamous Cell Carcinoma

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2
Q

Which metastasizes - Squamous Cell or Basal Cell?

A

Squamous Cell Carcinoma

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3
Q

Pearly nodule with rolled telangiectactic edge

A

Basal Cell Carcinoma

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4
Q

Strep throat infection –> tear-drop salmon-pink papules with fine scale, on trunk/limbs

A

Guttate Psoriasis

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5
Q

Psoriasis treatment

A

Dermol 500 cream –> Dovobet (calcipotriol + betamethasone)

Also: UV phototherapy, methotrexate

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6
Q

Seborrheic drematitis treatment

A

Ketoconazole 2% shampoo + olive oil

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7
Q

Single red lesion, with central clearing – what is best investigation?

A

KOH microscopy (tinea caused by dermatophytes)

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8
Q

Several itchy, hypopigmented lesions

A

Pityriasis Versicolor

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9
Q

Sharply-defined skin infections

A

Erysipelas (strep pyogenes)

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10
Q

Differentiate with herpes zoster ophthalmicus and Ramsay-Hunt?

A

Face paralysis in Ramsay-Hunt (shingles affecting facial nerve)

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11
Q

One red lesion with central clearing –> lots more across body

A
Pityriasis Rosea (HHV6/7)
One red lesion is Herald Patch
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12
Q

Rosacea treatment

A

Topical metronidazole

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13
Q

How to remember TB side effects

A

RifamPEEcin
IsoNERVEzid
PyraLIVERmide
EYEthambutol

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14
Q

HIV diagnosis

A

Combined HIV antibody and p24 antigen

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15
Q

Haemolytic Uraemic Syndrome triad

A

MAHA
AKI
Thrombocytopaenia

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16
Q

Cause of diarrhoea in a traveller

A

E. coli (ETEC)

17
Q

Chlamydia treatment

A

Doxycycline (or azithromycin)

18
Q

Gonorrhoeae treatment

A

IM ceftriaxone

19
Q

Haemantics in sideroblastic anaemia

A

Raised iron, raised ferritin

20
Q

Syphilis treatment

A

IM penicillin

21
Q

Pallor, jaundice, hepatosplenomegaly, overgrowth of maxillary bone

A

Beta thalassaemia (increased EPO = increased bone expansion)

22
Q

Where is B12 absorbed?

A

Terminal ileum (so affected by Crohn’s)

23
Q

Thrombotic Thrombocytopenia Purpura pentad

A

HUS + fever + CNS signs

24
Q

Thrombotic Thrombocytopenia Purpura

A

Plasmapheresis and steroids

25
Q

Genetics of sickle cell anaemia

A

Mutation in codon 6 of β-globin gene = glutamate to valine

26
Q

APTT = intrinsic or extrinsic pathway?

A

Intrinsic
 Haemophilia A or B
 vWD (carries factor 8)
 Unfractionated heparin

27
Q

PT = intrinsic or extrinsic pathway

A

Extrinsic
 Warfarin
 Hepatic failure

28
Q

Difference between warfarin compliance and overdose re. APTT and PT

A

Warfarin compliance = ↑PT, normal APTT

Warfarin overdose = ↑PT and ↑APTT

29
Q

Platelet transfusion indication

A

Normal: <10
Surgery: <50
Surgery in critical site: <100

30
Q

FFP vs cryoprecipitate

A
FFP = clotting factors 
Cryoprecipitate = fibrinogen – use when fibrinogen <1g/L (give 10 units)
31
Q

CML treatment

A

Imatinib (TKI)

32
Q

CLL treatment

A

Watch and wait… unless lymphos double every 6 months, B symptoms, bone marrow failure

33
Q

Auer rods

A

AML

34
Q

Sigmoid vs caecal volvulus treatment

A

Sigmoid: flatus tube insertion
Caecal: right hemicolectomy