Other Path Flashcards

1
Q

What is the main mechanism behind HSV resistance to antivirals?

A

Thymidine Kinase mutation

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2
Q

What is the main mechanism behind CMV resistance to antivirals?

A

Protein Kinase mutation

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3
Q

Which virus is most commonly implicated in infection post-transplant in paediatric populations?

A

Adenovirus

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4
Q

How is post-transplant adenovirus treated?

A

Brincidofovir

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5
Q

How is RSV infection treated?

A

Ribavarin

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6
Q

Which virus is implicated in post-transplant lymphoproliferative disease?

A

EBV

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7
Q

When would you not give Ganciclovir to treat CMV?

A

Post HCST, use Foscarnet

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8
Q

A patient who has recently been on a cruise in Japan, where they ate lots of raw seafood, presents with diarrhoea. What is the most likely causative organism?

A

Vibrio parahaemolyiticus

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9
Q

Give an example of an antibiotic class that is affected by altered target resistance.

A

Macrolides

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10
Q

Give an example of an antibiotic that is affected by bypass resistance.

A

Trimethoprim

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11
Q

What is a fungal eye infection most commonly found to be?

A

Candida endopthalmitis

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12
Q

How would you treat Candida spp. infections not caused by Candida albicans?

A

Echinocandin

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13
Q

Which Cryptococcus species infects immunocompetent hosts?

A

Cryptococcus gattii

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14
Q

Which Cryptococcus species infects immunosuppressed hosts?

A

Cryptococcus neoformans

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15
Q

A patient with pneumonia has a CXR, which shows a bat wing appearance. What is the most likely causative organism?

A

Pneumocystis jirovecii

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16
Q

How is Hepatitis C treated?

A

Interferon

Ribavarin

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17
Q

How are infected prosthetic joints managed?

A

Removal and debridement before Abx

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18
Q

A patient returns from a city break in Bangkok complaining of a new, sunburn like rash, a retro-orbital headache and myalgia. What is the most likely diagnosis?

A

Dengue Fever

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19
Q

In which infectious disease are ‘Purple eyelids’ a common feature?

A

Chagas Disease

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20
Q

In which infectious disease are ‘Negri Bodies’ seen?

A

Rabies

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21
Q

Name two classes of drug which may be used to treat Benign prostatic Hyperplasia.

A

5-alpha reductase inhibitor

Alpha Blocker

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22
Q

In which disease might there be a mutation affecting Superoxide Dismutase 1?

A

Motor Neurone Disease

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23
Q

How would you manage a Pseudomonas aeruginosa infection?

A

Gentamicin

Ceftazadine

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24
Q

Which disease’s severity would be assessed using the Breslow Score?

A

Melanoma

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25
Q

Which organism is the most common cause of bronchopneumonia?

A

Haemophilus influenzae

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26
Q

Which organism is the most common cause of CNS infections overall?

A

Coxsackie virus

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27
Q

Which organism most commonly causes lung disease in patients with Cystic Fibrosis?

A

Pseudomonas aeruginosa

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28
Q

Which tapeworm species is found in pigs?

A

Taenia solium

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29
Q

Which tapeworm species is found in cows?

A

Taenia saginata

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30
Q

Which type of worm’s life cycle involves migrating from the skin to the bowel, laying eggs, hatching as rhabitiform larvae and maturing into filariform larvae?

A

Strongyloide (Pinworm), type of Nematode (soil-based)

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31
Q

Which type of worm’s life cycle involves being eaten, living in the intestines, forming a cyst and the cyst releasing a tapeworm, which grows and releases more eggs?

A

Cestodes (Tapeworm)

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32
Q

Which type of worm’s life cycle involves cercariae invading the skin after being released by freshwater snails, worms developing in the liver, migrating to the mesenteric venules/venous plexus of bladder, laying eggs which become miricidia and reinfecting freshwater snails?

A

Trematode (Schistosomiasis)

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33
Q

How would you treat strongyloide infection?

A

Ivermectin

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34
Q

Which medication is most widely used for parasitic infection?

A

Praziquantel

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35
Q

The centre of a granuloma being diffuse red indicates what?

A

Necrosis

Caseation

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36
Q

At what level must skin damage be to leave a scar?

A

Dermis

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37
Q

Where is the dermis in relation to the basement membrane?

A

Sits below it

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38
Q

Which virus is associated with Nasopharyngeal Carcinoma?

A

EBV

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39
Q

Which toxins are associated with Hepatocellular Carcinoma?

A

Aflatoxins

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40
Q

What is the role of stellate cells in the liver?

A

Vitamin A stores

Activate to myofibroblasts to lay down collagen

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41
Q

What does ‘Grade’ mean with regards to Chronic Hepatits?

A

Severity of inflammation

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42
Q

What does ‘Stage’ mean with regards to Chronic Hepatitis?

A

Severity of Fibrosis

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43
Q

What is the most common form of carcinoma that arises from CIN changes?

A

Squamous Cell Carcinoma

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44
Q

In which breast cancer are large, pleomorphic cells seen?

A

Invasive Ductal

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45
Q

In which breast cancer are Indian Files seen?

A

Invasive Lobular

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46
Q

In which breast cancer are Elongated Tubules seen?

A

Invasive Tubular

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47
Q

In which breast cancer are Empty Spaces seen?

A

Invasive Mucinous

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48
Q

What is the most important prognostic factor for Breast Cancer?

A

Spread to axillary lymph nodes

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49
Q

Which stain is used to distinguish Squamous Cell Carcinomas from Adenocarcinomas?

A

P40

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50
Q

In which condition would you see ‘Soap Bubble Osteolysis’ on x-ray, with ‘Chinese Letters and Shepherd’s Crook’ Signs?

A

Fibrous Dysplasia

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51
Q

In which syndrome would you see polyostotic fibrous dysplasia and rough border Cafe au Lait spots?

A

McCune Albright Syndrome

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52
Q

Which benign bone tumour typically affects teenage boys and occurs at the end of long bones?

A

Osteochondroma

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53
Q

Which benign bone tumour occurs in hands and feet and shows ‘popcorn calcification’ on x ray?

A

Enchondroma

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54
Q

Which benign bone tumour mainly affects young women and occurs at the epiphyses of long bones? On histology, there are osteoclasts on a background of spindle/ovoid cells.

A

Giant Cell tumour

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55
Q

What is the most common bone sarcoma?

A

Osteosarcoma

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56
Q

Which malignant bone tumour shows ‘Codman’s Triangle and a sunburst appearance’ on x-ray and malignant mesenchymal cells on histology?

A

Osteosarcoma

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57
Q

Which malignant bone tumour produces cartilage, and on histology shows ‘Malignant chondrocytes with or without chondroid matrix’?

A

Chondrosarcoma

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58
Q

Which malignant bone tumour shows ‘onion skinning of the periosteum’ on x-ray, and ‘sheets of small round cells’ on histology?

A

Ewing’s Sarcoma

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59
Q

Which tumour is associated with t(11;22)(q24;q12)?

A

Ewing’s Sarcoma

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60
Q

How are cytopathological samples of Breast cancers graded?

A

C1-5

1: Inadequate
2: benign
3: Atypia, probably benign
4: Atypia, probably malignant
5: malignant

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61
Q

Which disease shows proteinaceous material and neutrophils on cytology, and duct distension with proteinaceous material and ‘foamy macrophages’ on histology?

A

Duct Ectasia

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62
Q

Which breast disease shows neutrophils on cytology, and is usually caused by Staphylococcus aureus?

A

Acute Mastitis

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63
Q

Which breast disease shows ‘fat cells surrounded by macrophages’ on cytology?

A

Fat Necrosis

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64
Q

Which breast disease shows ‘dilated, calcified ducts’ on histology.

A

Fibrocystic Disease

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65
Q

Which breast disease shows ‘glandular and stromal cells’ on histology, and presents as a mobile, well circumscribed lump?

A

Fibroadenoma

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66
Q

Which breast condition shows ‘overlapping cells’ on histology, and is benign? It is sometimes described as having a ‘leaf-like’ appearance.

A

Phyllode’s Tumour

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67
Q

Which benign breast tumour may present with bloody nipple discharge?

A

Central Intraductal Papilloma

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68
Q

Which breast condition shows:

Cytology: Clusters of cells

Histology: Dilated ducts, polypoid mass in the middle
?

A

Intraductal Papilloma

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69
Q

Which breast condition may show ‘a central stellate area’ and a ‘proliferation of ducts and acini’ on histology?

A

Radial Scar

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70
Q

List 3 types of proliferative breast disease.

A

Usual Epithelial Hyperplasia
Flat Epithelial Atypia/Ductal Carcinoma
In situ lobular neoplasia

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71
Q

Which breast condition shows ‘cribiform, punched out;’ appearance on histology, with compact lumens, calcification and overlapping cells?

A

Low grade Ductal carcinoma in situ

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72
Q

Which breast condition shows a ‘central lumen of necrotic tissue’ with large cells, pleiomorphic cells which occlude a duct, and few lumens?

A

High grade ductal carcinoma in situ

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73
Q

Which breast cancer shows ‘pleiomorphic cells with large nuclei’ on histology and is E-cadherin +ve?

A

Invasive Ductal Carcinoma

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74
Q

Which breast cancer shows a ‘linear, Indian File pattern’ on histology, with a monomorphic appearance?

A

Invasive Lobular Carcinoma

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75
Q

Which breast cancer shows ‘elongated tubules invading the stroma’ on histology?

A

Invasive tubular carcinoma

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76
Q

Which breast cancer shows ‘empty spaces with lots of mucin’ on histology?

A

Invasive mucinous carcinoma

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77
Q

Which breast cancer shows ‘sheets of markedly atypical cells, with prominent lymphocytic infiltrates and central necrosis’ on histology?

A

Basal-Like Carcinoma

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78
Q

Which gene mutation is a poor prognostic indicator for breast cancer?

A

Her2

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79
Q

Which gene mutation is a good prognostic indicator for breast cancer?

A

ER/PR

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80
Q

In which thyroid condition might you see calcifications (psammoma bodies) and clear nuclei (Orphan’s Annie Eyes)?

A

Papillary Thyroid Cancer

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81
Q

In which thyroid condition might you see amyloid deposition with Congo Red staining, and why?

A

Medullary Carcinoma

Calcitonin breaks down to Amyloid

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82
Q

What effect does PTH have?

A

1-alpha Hydroxylase activation
Osteoclast activation
Renal calcium resorption
Renal potassium excretion

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83
Q

What is secreted in the Zona Glomerulosa?

A

Aldosterone

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84
Q

What is secreted in the Zona Fasciculata?

A

Glucocorticoids

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85
Q

What is secreted in the Zona Reticularis?

A

Androgens & Glucocorticoids

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86
Q

What is secreted in the Zona Medulla?

A

Noradrenaline

Adrenaline

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87
Q

What is Waterhouse Friederichson Syndrome?

A

Haemorrhage into adrenals due to septic DIC = acute adrenal insufficiency

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88
Q

Non-infective endocarditis caused by SLE?

A

Libman-Sacks Endocarditis

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89
Q

Which vasculitis characteristically shows a ‘rosary beads’ appearance on angiogram due to multiple aneurysms?

A

Polyarteritis Nodosa

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90
Q

What is c-ANCA directed against?

A

Proteinase 3

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91
Q

What is p-ANCA directed against?

A

Myeloperoxidase

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92
Q

Which vasculitis shows ‘narrowing of the lumen and lymphocytic infiltration of the tunica media’ on biopsy?

A

Temporal Arteritis

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93
Q

Which staging system is used for Cervical Cancer?

A

FIGO

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94
Q

Name one mutation that is associated with Type I endometrial carcinoma.

A

PTEN

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95
Q

Which mutation is associated with serous endometrial carcinoma?

A

p53

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96
Q

Which cancer is most strongly associated with endometriosis?

A

Ovarian clear cell carcinoma

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97
Q

How does an artheroma form?

A

Endothelial Injury -> LDL Aggregation

Monocyte Adhesion

Monocyte migration into intima

Platelet Adhesion

Lipid Accumulation

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98
Q

What does MI histology show in the first 6 hours?

A

Normal

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99
Q

What does MI histology show between 6-24 hours?

A

Coagulative Necrosis
Loss of Nuclei
Striations

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100
Q

What does MI histology show 1-4 days?

A

Infiltration of neutrophils & macrophages

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101
Q

What does MI histology show 5-10 days?

A

Macrophages

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102
Q

What does MI histology show 10-14 days?

A

Granulation, Angiogenesis, Collagen Synthesis

Myofibroblasts, Macrophages, Angioblasts

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103
Q

What is the most common cause of aortic stenosis?

A

Calcification

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104
Q

Which disease in children shows ‘effacement of foot processes’ on electron microscopy?

A

Minimal Change Disease

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105
Q

Which renal disease shows ‘partially scarred glomeruli’ and ‘thickened GBM’?

A

Focal Segmental Glomerulosclerosis

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106
Q

Which renal disease shows immune deposits on the outside of the glomerular basement membrane and thickening of the BM?

A

Membranous Glomerulonephritis

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107
Q

Which antibody is associated with membranous glomerulonephritis?

A

Anti-phospholipase A2 type M receptor

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108
Q

How is Alport’s Syndrome inherited, and what does the mutation affect?

A

X-linked dominant

alpha 5 subunit of type iv collagen

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109
Q

In which renal condition might you see ‘shrunken kidneys with granular cortices’ and ‘fibrinoid necrosis’?

A

Hypertensive Nephropathy

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110
Q

Poisoning with which chemical may predispose to Calcium Oxalate crystal formation?

A

Ethylene Glycol

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111
Q

In which syndrome might you see Renal Oncocytomas?

A

Birt-Hogg-Dube Syndrome

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112
Q

Which benign renal tumour is epithelial in origin and composed of papules and tubules?

A

Papillary Adenoma

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113
Q

Which benign renal tumour is epithelial in origin and composed of oncocytic cells?

A

Renal Oncocytoma

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114
Q

Which benign renal tumour is mesenchymal in origin and composed of thick walled blood vessels, smooth muscle and fat?

A

Angiomyolipoma

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115
Q

Which malignant renal tumour appears grossly as a ‘golden yellow tumour’ with ‘haemorrhagic areas’?

A

Clear Cell Carcinoma

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116
Q

Which malignant renal tumour is associated with long-term dialysis and appears as a ‘fragile, friable, brown tumour’?

A

Papillary Renal Cell Carcinoma

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117
Q

Which malignant kidney tumour appears as a well circumscribed solid brown tumour?

A

Chromophobe Renal Cell Carcinoma

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118
Q

Which renal tumour appears as ‘small, round, blue cells’ on histology?

A

Nephroblastoma

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119
Q

How is prognosis for Prostatic Adenocarcinoma calculated?

A

Gleason Score

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120
Q

What might it indicate if a lung lobe isn’t black on autopsy?

A

Pneumonia

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121
Q

When would you refer a death to the coroner?

A
Unknown COD
Sudden death (<24h in hospital)
Suspicious
Self-Neglect/Suicide
Related to detainment/Medical care
Related to job
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122
Q

Which antibody is implicated in Bullous Pemphigoid?

A

Anti-Hemidesmosome, attacking basememnt membrane

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123
Q

Where is the site of disease in Pemphigus Vulgaris?

A

Dermal-epidermal junction

IgG attacks between keratin layers

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124
Q

In which IgG mediated skin condition might the outer layer of the stratum shear off?

A

Pemphigus follaceous

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125
Q

Which skin condition is characterised pathologically by thickened epidermis, parakeratosis layers, disappeared stratum granulosum and Munro’s microabscesses?

A

Psoriasis

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126
Q

How does Lichen Planus present:

a) on the wrists/arms
b) in the mouth?

A

a) Purplish/red rash

b) White Lines (Wickham Striae)

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127
Q

In which condition might you see ‘horn cysts’, which are areas where the epidermis entraps keratin?

A

Seborrhoeic Dermatitis

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128
Q

What occurs in the immediate phase of asthma?

A

Mast cell degranulation and effects

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129
Q

What occurs in the late phase of asthma?

A

Tissue damage, mucous production, muscle hypertrophy

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130
Q

In which lung condition might you find ‘iron-laden macrophages’ on histology?

A

Pulmonary Oedema

From the heart

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131
Q

What are the stages of lobar pneumonia?

A

Congestion
Red Hepatisation
Grey Hepatisation
Resolution

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132
Q

What is the key feature of grey hepatisation in pneumonia?

A

Intra-alveolar neutrophils

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133
Q

What are the stages of fracture repair?

A

Haematoma
Fibrocartilaginous callus
Mineralisation of callus
Remodelling

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134
Q

In which bone disease might you see ‘Langerhans-type Giant Cells with horseshoe nuclei’?

A

TB

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135
Q

In which condition might you see a proliferative synovitis, with pannus formation and grimley sokoloff cells on histology?

A

Rheumatoid Arthritis

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136
Q

Which cells are present in MALTomas related to H Pylori?

A

B Cells

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137
Q

Which cells are present in Duodenal Lymphomas?

A

T Cells

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138
Q

What is the most common genetic predisposition to brain tumours?

A

Neurofibromatosis

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139
Q

What is the most common paediatric brain cancer?

A

Pilocytic Astrocytoma

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140
Q

Which brain tumour is cerebellar and well circumscribed on MRI, and shows hairy piloid cells and rosenthal fibres on histology?

A

Pilocytic Astrocytoma

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141
Q

Which mutation is associated with Pilocytic Astrocytoma?

A

BRAF mutation

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142
Q

What is the most common primary brain cancer in adults?

A

Glioblastoma Multiforme

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143
Q

How do astrocytomas progress?

A

Become Glioblastomas

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144
Q

Which brain cancers are associated with IDH1/2 mutations?

A

Diffuse Astrocytoma

Oligodendroglioma

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145
Q

Which brain cancer displays ‘round cells with clear cytoplasm’ (fried egg appearance)

A

Oligodendroglioma

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146
Q

Which brain cancer shows ‘small blue round cells’ and ‘Horner-Wright Rosettes’?

A

Medulloblastoma

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147
Q

How is tau spread staged in Alzheimer’s?

A

Braak Staging

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148
Q

Which three enzymes are involved in oxidative killing by granulocytes?

A

NADPH Oxidase
Superoxide Dismutase
Myeloperoxidase

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149
Q

Which antigen is found on all T Cells?

A

CD3

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150
Q

Which T Cells play a key role in germinal centre reactions and Plasma Cell class switching?

A

T Follicular Helper Cells

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151
Q

Which T Cells express FoxP3 and CD25?

A

T Regulatory

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152
Q

Which T Cells express CD4 and secrete IFN-y and IL-2

A

T Helper 1

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153
Q

Which chemokines help direct dendritic cells to lymph nodes?

A

CCL19 CCL21

ligands for CCR7

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154
Q

Which agent used in FMF binds to tubulin in neutrophils?

A

Colchicine

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155
Q

Which HLA is seen in Goodpasture’s Syndrome?

A

HLA DR15

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156
Q

Which cytokine plays a key role in development of TH2 cell responses (and hence allergic responses)?

A

IL-4

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157
Q

Which cell type does Azathioprine target?

A

T

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158
Q

Which cell type does Cyclophosphamide target?

A

B

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159
Q

Which cell type does mycophenolate motefil target?

A

T

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160
Q

Which enzyme’s activity must be checked before starting Azathioprine?

A

TPMT

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161
Q

Name a JAK inhibitor.

A

Tofacitinab

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162
Q

What does Secukinumab target?

A

IL-17

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163
Q

What does Guselkumab target?

A

IL-23

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164
Q

What does Ustekinumab target?

A

IL12 IL23

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165
Q

What does Abatacept target?

A

CTLA4-Ig fusion gene

RA if Anti-tnf alpha ineffective

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166
Q

What is the max number of HLA mismatches between a parent and child?

A

3

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167
Q

What is the max number of mismatches between siblings?

A

3

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168
Q

What are the 3 phases of antibody mediated transplant rejection?

A

1: exposure to antigen
2: B Cell proliferation and maturation
3: Effector = antibodies bind to graft epithelium

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169
Q

What are the phases of T cell-mediated graft rejection?

A

1: Activate alloreactive T Cells
2: Normal T Cell functions vs graft
Effector: T cells tether graft endothelium and attack tubular epithelium.

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170
Q

What are the histological features of T-cell mediated graft rejection?

A

Lymphocytic interstitial infiltration
Ruptured tubular basement membrane
Tubulitis
Macrophages

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171
Q

What are the cardinal features of antibody-mediated rejection?

A

Capillaritis

Inflammatory cells in the capillaries

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172
Q

What is there a deficiency of in Leukocyte Adhesion Deficiency?

A

CD18

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173
Q

Which immunodeficiency may be implicated in a child presenting with recurrent, severe viral infections?

A

NK Deficiency

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174
Q
A patient has:
Low/Absent T
Low/Absent NK
Normal/High B
Low Ig
What is the likely cause?
A

X-linked SCID

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175
Q
A patient has:
Low/Absent T
Low/Absent NK
Low/Absent B
Low Ig
Normal Neutrophils
What is the likely cause?
A

ADA Deficiency

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176
Q
A patient has:
Low CD4
Normal CD8
Normal B
Low IgG/IgA
What is the likely cuase?
A

Bare Lymphocyte Syndrome II

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177
Q

How might you differentiate between IDA and Beta Thalassaemia trait on blood film?

A

Basophilic Stippling = BT

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178
Q

How is anaphylaxis managed?

A
ABC
Mask O2
IM Adrenaline
IV Antihistamine
Nebulised Bronchodilators
IV Corticosteroids
IV Fluids
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179
Q

What does normal levels of C3/4, but absent CH50/AP50 represent?

A

Deficiency in common pathway

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180
Q

Which Staph is coagulase positive?

A

Staph aureus

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181
Q

Which Staph is coagulase negative?

A

epidermidis

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182
Q

Which bacteria are gram positive bacilli?

A
ABCDL
Actinomyces
Bacillus
Clostridium
Diptheria
Listeria
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183
Q

Which bacteria are gram negative cocci?

A

Neisseria spp

Moraxella

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184
Q

Which bacteria are gram negative cocobacilli?

A
Haemophilus
Bordatella
Pseudomonas
Chlamydia
Brucella
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185
Q

Which antibiotics are considered broad-spectrum?

A
'These meds can cover'
Tazocin
Meropenem
Co-amoxicvlax
Ciprofloxacin
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186
Q

Which pneumonia cause shows ‘glossy colonies’ on agar?

A

Haemophilus influenzae

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187
Q

Which cause of pneumonia is cold agglutinin +ve?

A

Mycoplasma pneumoniae

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188
Q

Trophozoite with 4 nuclei, flask-shaped ulcer?

A

Entamoeba Histolytica

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189
Q

Trophozoite with 2 nuclei, pear-shaped ulcer?

A

Giardia Lamblia

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190
Q

What is the mechanism of action of aciclovir and ribavarin?

A

Nucleoside Analogue

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191
Q

Which disease is transmitted by the Tsetse Fly?

A

Trypanasoma

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192
Q

Which disease is transmitted by the Sand Fly?

A

Lesihmania

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193
Q

Which mutation is associated with MAHA and TTP?

A

ADAMTS13 = VWF cleaving protease deficiency

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194
Q

What are the three main causes of MAHA?

A

Adenocarcinoma
HUS
TTP

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195
Q

What effect does Protein C have?

A

Anti-thrombotic

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196
Q

What is the mechanism of action of warfarin?

A

Vitamin K epoxide reductase inhibitor

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197
Q

How is warfarin monitored?

A

INR

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198
Q

How is LMWH monitored in patients with renal failure/extremes of weight?

A

Anti-Xa assay

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199
Q

In which order do factors drop after commencing warfarin?

A

7, C, 9, 10, 2

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200
Q

Which type of patient might benefit most from long term anticoagulation after a DVT?

A

M>F

Idiopathic

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201
Q

Which factor falls in pregnancy?

A

S

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202
Q

Rank B-Cell NHLs from most to least aggressive.

A
Burkitt's
Mantle
Diffuse large B Cell
Marginal Zone
Small Lymphocytic 
Follicular
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203
Q

Which diagnostic markers are used for Hodgkin’s Lymphoma?

A

CD30

CD15

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204
Q

Which cancer is likely to be present if B Cells expressing CD5 but not CD19 are found in the peripheral blood?

A

CLL

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205
Q

When would you treat CLL?

A

Progressive disease
Massive splenomegaly
Massive Lymphadenopathy
B Symptoms

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206
Q

What might cause psuedopolycythaemia?

A

Alcohol
Obesity
Diuretics

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207
Q

What might cause a polycythaemia with an appropriately high EPO?

A

Altitude

Hypoxic Lung Disease

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208
Q

What might cause a polycythaemia with an inappropriately high EPO?

A

Renal Disease

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209
Q

Which pharmacological agent might be used in the treatment of polycythaemia vera?

A

Hydroxycarbimide

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210
Q

A patient presents with an isolated mild thrombocythaemia. They regularly suffer from headaches, What is the most likely diagnosis?

A

Essential thrombocythaemia

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211
Q

A man with CML is found to have between 10-19% blasts on blood film. Which stage of disease is he said to be in?

A

Accelerated Phase

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212
Q

A man with CML is found to have over 20% blasts on blood film. Which stage of disease is he said to be in?

A

Blast Crisis

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213
Q

In which group of conditions might you see ringed sideroblasts and bi-lobed neutrophils?

A

Myelodysplastic Syndromes

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214
Q

How might you treat myelodysplastic syndromes?

A

Allogenic Stem cell Transplant

Chemo

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215
Q

How do people with myelodysplastic syndrome die?

A

Third each
Infection
Bleeding
Acute Leukaemia

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216
Q

What is the most common cause of Aplastic Anaemia?

A

Idiopathic

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217
Q

What might cause congenital Aplastic Anaemia?

A

Fanconi Anaemia

Dyskeratosis Congenita

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218
Q

What is aplastic anaemia?

A

Failure of pleuipotent stem cells -> Pancytopaenia

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219
Q

What does the bone marrow look like in aplastic anaemia?

A

Hypocellular

Fatty

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220
Q

What shortens in dyskeratosis congenita?

A

Telomere

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221
Q

When is a red cell transplant indicated?

A

If >30% blood lost
Hb below 70 peri-operatively
Symptomatically

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222
Q

When might you transfuse washed cells?

A

If patients have severe allergic reactions to blood products

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223
Q

What does blood irradiation do?

A

Destroys donor lymphocytes to prevent GvHD in immunosuppressed people

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224
Q

When is fresh frozen plasma indicated?

A

Massive blood loss (>150ml/min)
DIC with bleeding
Liver disease with PT 1.5x normal

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225
Q

A patient develops chills, rigors and fever of 37.8 degrees during a blood transfusion. Your consultant says a reaction has taken place due to the release of cytokines by white cells in blood storage. Which reaction has taken place?

A

Febrile non-haemolytic transfusion reaction

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226
Q

A patient develops a mild itchy rash and a wheeze during a fresh frozen plasma transfusion. What is the likely diagnosis?

A

Allergic reaction

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227
Q

A patient develops pulmonary oedema shortly after undergoing a blood transfusion. What is the most likely diagnosis?

A

Transfusion-associated circulatory overload

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228
Q

A patient develops SOB, low sats and tachycardia 4 hours after undergoing a transfusion. CXR shows pulmonary infiltrates. What is the most likely diagnosis?

A

Transfusion-associated acute lung injury

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229
Q

A patient who regularly undergoes blood transfusions for Beta-Thalassaemia becomes jaundiced and anaemic 2 days after their most recent treatment. They also notice dark urine. What is the most likely diagnosis?

A

Delayed Haemolytic Transfusion Reaction

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230
Q

What is the mechanism behind delayed haemolytic transfusion reactions?

A

Develop new antibodies vs RBCs (Alloimunisation)

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231
Q

What is the prognosis of GVHD?

A

Mostly fatal

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232
Q

What is used as a marker of stem cells?

A

CD34

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233
Q

How does chronic GVHD present?

A

Similarly to Sjogren’s

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234
Q

What disease causes HbSC?

A

Sickle Cell/Haemoglobin C disease, which causes milder sickling than HbSS

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235
Q

Which disease might cause anaemia via a glycolytic pathway enzyme deficiency?

A

Pyruvate Kinase Deficiency

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236
Q

In which leukaemia might you see an abundance of promyelocytes with auer rods on blood film?

A

Acute Promyelocytic Leukaemia

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237
Q

How would you conclusively distinguish between acute leukaemias?

A

Immunophenotyping

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238
Q

What is the normal range for potassium?

A

3.5-5.5 mmol/L

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239
Q

What is the normal range for sodium?

A

135-145 mmol/L

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240
Q

What is the normal range for haemoglobin in men?

A

130-180 g/L

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241
Q

What is the normal range for haemoglobin in women?

A

115-160 g/L

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242
Q

What is the normal range for calcium?

A

2.2-2.6 mmol/L

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243
Q

A patient presents with metabolic acidosis, an isolated hypokalaemia and renal stones. What is the likely diagnosis?

A

Type 1 Renal Tubular Acidosis

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244
Q

Which drug, used in chronic management of gout, increases the fractional excretion of uric acid?

A

Probenecid

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245
Q

What causes a raised anion gap metabolic acidosis?

A
GOLDMARK
Glycols
Oxoproline
L-lactate
D-lactate
Methanol
Aspirin
Renal Failure
Ketoacidosis
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246
Q

What condition describes inadequate function of the proximal renal tubules of the kidney and is associated with glucosuria, hypophosphataemia and hyperuricosuria?

A

Fanconi Syndrome

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247
Q

Which enzyme converts Cholesterol into Cholesterol ester?

A

ACAT

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248
Q

Which agent is best at reducing LDL levels in the blood?

A

Evolocumab

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249
Q

What may cause a gout attack in the knee?

A

Saturnine Gout - Lead Poisoning

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250
Q

Which condition might cause hypocholesterolaemia and orange tonsils in children?

A

Tangier Disease

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251
Q

How might you distinguish between true and pseudo hyponatraemias?

A

Serum osmolality - should be low

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252
Q

Which sign, often seen in hypocalcaemia, involves tapping the facial nerve and visualising ipsilateral contraction of the facial muscles?

A

Chvostek’s Sign

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253
Q

What might cause an unexplained metabolic acidosis with both a raised anion gap and osmolar gap?

A

Glycol, Ethanol, Mannitol, Methanol Poisoning

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254
Q

Which enzyme is the rate limiting step in de novo purine synthesis?

A

PAT

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255
Q

Which autosomal recessive disorder leads to an increase in blood plant sterols?

A

Phytosterolaemia

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256
Q

What might cause a normal anion gap metabolic acidosis?

A

Addisons
Bicarbonate Loss
NaCl infusion
Drugs

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257
Q

What might cause a false lymphocytosis to show on FBC?

A

Presence of reticulocytes

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258
Q

What might cause p-wave flattening, hyperacute t waves and a broad QRS in a patient undergoing chemotherapy?

A

Hyperkalaemia due to tumour lysis syndrome

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259
Q

Does haemophilia affect the bleeding time?

A

No

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260
Q

Which blood film finding is caused by paraproteinaemia in MM?

A

Rouleaux formation

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261
Q

What complication are patients with essential thrombocytosis at risk of?

A

Stroke

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262
Q

Which syndrome is characterised by neutropenia, pancreatic dysfunction and short stature?

A

Shwachmann Diamond Syndrome

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263
Q

Which bone marrow failure syndrome is characterised by an isolated failure of red cell production, presenting as a macrocytic anaemia and low reticulocytes?

A

Diamond-Blackfan Syndrome

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264
Q

What is the most sensitive marker for iron deficiency anaemia?

A

Low Serum Ferritin

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265
Q

Which anticoagulant would you use in a patient with DVT and renal failure?

A

Warfarin

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266
Q

Which medication may be used as prophylaxis for tumour lysis syndrome?

A

Rasburicase

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267
Q

Which drug can be used to treat M3 AML (Acute promyeloytic leukaemia)?

A

All Trans Retinoic Acid

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268
Q

Which condition causes progressively falling platelet counts in a patient started on heparin (enoxaparin)?

A

Heparin induced Thrombocytopaenia

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269
Q

Why does tumour lysis syndrome cause hypocalcaemia?

A

Released phosphate binds free calcium in the serum

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270
Q

In which cell type are auer rods seen?

A

Neutrophil

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271
Q

Which oncogene is found in Burkitt’s, and is formed by a t(8;14) mutation?

A

C-MYC

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272
Q

Which lobe is most commonly affected in HSV encephalitis?

A

Temporal

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273
Q

Which cancer shows ‘oat-shaped cells’ on biopsy?

A

Small cell lung cancer

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274
Q

How many stages of CKD are there?

A

5

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275
Q

What do delta cells of the pancreas secrete?

A

Somatostatin

276
Q

What is Von Hippel Lindau Syndrome?

A
Brain Haemangiomas
Renal Cysts
Neuroendocrine tumours
Clear Cell Tumours
Phaeochromocytomas
277
Q

A patient with a recent history of head trauma causing LOC experiences a lucid interval followed by deterioration. Which pathology is this most likely to represent?

A

Extradural Haemorrhage

278
Q

Which syndrome is characterised by nephritic syndrome, cataracts and sensironeural deafness?

A

Alport’s

279
Q

What is the first line chemotherapy for prostate cancer?

A

Docetaxel

280
Q

What condition may be present if ‘waxy casts’ are found in urine?

A

CKD

281
Q

Kimmelstiel Wilson nodules found in a renal biopsy are associated with what underlying disease?

A

Diabetes

282
Q

A renal biopsy reads “Thickened basement membrane with spike and dome appearance due to electron dense deposits in the subepithelial layer”. What is the most likely diagnosis?

A

Membranous Glomerulonephritis

283
Q

Name the first line treatments for Wilson’s Disease.

A

Zinc

Trientine

284
Q

In which gross anatomical section of the pancreas does pancreatic cancer typically occur?

A

Head

285
Q

What are the most common cancers in the UK in men/women?

A

Men:

Prostate (most common in men)
Lung
Bowel
Head and Neck

Women:

Breast (most common cancer overall)
Lung
Bowel
Uterus

286
Q

The ECG leads V1 and V2 represent which specific region of the heart?

A

Septal

287
Q

What might cause AST to be over 3x higher than ALT?

A

Alcoholic Hepatits

288
Q

What might cause ALT to be in the thousands?

A

Paracetamol/Toxins
Viruses
Ischaemia

289
Q

What might cause a mildly elevated ALT?

A

Fatty Liver

290
Q

Which medication might cause hepatic adenomas?

A

COCP

291
Q

Which condition is associated with the presence of fatty casts in urine?

A

Nephrotic Syndrome

292
Q

Which protein is defective in Polycystic Kidney Disease?

A

Polycystein-1

293
Q

What is the name of the criteria used to diagnose rheumatic fever?

A

Jones’

294
Q

What is the triad seen in carcinoid syndrome?

A

Bronchoconstriction
Flushing
Diarrhoea

295
Q

The ECG leads II, III and aVF represent which region of the heart?

A

Inferior

296
Q

An immune response directed against myelin basic protein and proteo-lipoprotein results in what autoimmune condition?

A

Multiple Sclerosis

297
Q

Which cause of nephrotic syndrome doesn’t respond to high dose steroids?

A

Membranous Glomerulonephritis

298
Q

What condition is the presence of granular (“muddy brown”) casts in the urine associated with?

A

Acute Tubular Necrosis

299
Q

What condition is the presence of epithelial casts in urine associated with?

A

Acute Tubular Necrosis

300
Q

What is the diagnostic criteria for common variable immunodeficiency?

A

Decrease in IgG and one of IgA/M

Lack of antibody response to antigens or immunisation

301
Q

What protein is defective in X linked Severe Combined Immunodeficiency?

A

Common gamma chain of IL2 receptor

302
Q

Which autoantibody is associated with ITP?

A

Anti-glycoprotein IIb

303
Q

What gene is defective in Bruton’s agammagobulinaemia?

A

BTK

304
Q

Which cytokine is predominantly responsible for T cell proliferation and survival?

A

IL-2

305
Q

CD14 is typically a marker of what type of immune cell?

A

Monocytes/Macrophages

306
Q

What is the likely cause of a rapidly progressive glomerulonephritis and nosebleeds/haemoptysis?

A

Granulomatosis with Polyangiitis

307
Q

Which organisms are people with chronic granulomatous disease susceptible to?

A
Catalase positive 
E Coli
Staph a
Listeria
Klebsiella
Candida
308
Q

Which stain is used for Pneumocystis?

A

Silver/Periodic acid-Schiff

309
Q

Which stains are used for Candida?

A

Periodic Acid Schiff or Methenamine Silver

310
Q

Which stains are used for Aspergillus?

A

Methenamine Silver

PAS

311
Q

What might Q Fever progress to?

A

Atypical Pneumonia
ARDS
Endocarditis

312
Q

How is Lyme Disease treated?

A

Doxycycline

313
Q

How is Leishmaniasis treated?

A

Amphotericin B

314
Q

Antibiotics - what does ceph- indicate?

A

Cephalosporin

315
Q

ABx - what does -floxacin indicate?

A

Quinolone

316
Q

Which malaria species causes fevers every 3 days?

A

Plasmodium malariae

317
Q

Which organism causes Q Fever?

A

Coxiella Burnetti

318
Q

Which antibiotic is used to treat BV?

A

Metronidazole

319
Q

Which species causes Lyme Disease?

A

Borellia Burgdoreffi

320
Q

Rash after fish bite organism?

A

Mycoplasma marinum

321
Q

What is the gold standard investigation for Leishmaniasis?

A

Splenic Aspirate

322
Q

The presence of galactomannan in the serum of a septic patient suggests the presence of what organism?

A

Aspergillus

323
Q

Which organism causes Chancroid?

A

Haemophilus ducreyi

324
Q

What can you mix toenails with to test for Tinea/Trichophytum presence?

A

Potassium Hydroxide

325
Q

A sexually active homosexual man received treatment two hours ago for genital primary syphilis. He was given a single of dose of IM benzylpenicillin. He presents to the emergency department reporting he has become unwell, with a fever, headache and muscle aches. He is concerned he is having an allergic reaction. He is pyrexial at 38C and his blood pressure is 98/76.

What syndrome is he suffering from?

A

Jarisch Herxeimer Syndrome

326
Q

What type of Hypersensitivity is Mixed Essential Cryoglobulinaemia, and which disease is it associated with?

A

Hepatitis C

III

327
Q

What is Evan’s Syndrome?

A

Type II HS

Autoimmune Haemolytic Anaemia + ITP

328
Q

Which antigen is targeted in Autoimune Thrombocytopaenic Purpura?

A

Glycoprotein IIb/IIIa on Platelets

329
Q

Which antigen is targeted in Pemphigus Vulgaris?

A

Epidermal Cadherin

330
Q

Which syndrome causes Hepatic Jaundice and is caused by a mutation in the UGT1A1 gene?

A

Criggler-Najjar Syndrome

331
Q

What is Turcot Syndrome?

A

Gliobastoma Multiforme
Medulloblastoma
Pineoblastoma

332
Q

What is Li-Fraumeni Syndrome?

A

Astrocytoma, PNET, Sarcomas, Breast Cancer, Leukaemia

333
Q

Which condition is associated with optic gliomas, neurofibromas and astrocytomas?

A

Neurofibromatosis Type I

334
Q

Which condition is associated with vestibular schwannomas, meningiomas, ependyomas and astrocytomas?

A

Neurofibromatosis Type II

335
Q

Which condition is associated with Giant Cell Astrocytomas, Cortical Tubers, Superendymal Nodules and calcifications on CT?

A

Tubular Sclerosis

336
Q

Which syndrome presents with parkinsonism, dystonia, apraxia and ‘alien limbs’ phenomenon?

A

Corticobasal Syndrome

337
Q

Which Parkinson Plus Syndrome presents with early autonomic dysfunction?

A

Multiple System Atrophy

338
Q

Which Parkinson Plus syndrome is associated with early falls, axial rigidity, akinesia, dysarthria and dysphagia?

A

Progressive Supranuclear Palsy

339
Q

Which chromosome is Frontotemporal Dementia associated with?

A

17

340
Q

Which condition describes behavioural changes associated with spherical inclusion bodies found in the cytoplasm on autopsy?

A

Pick’s Disease

341
Q

What is Aphasia?

A

Language disorder

342
Q

What is Apraxia?

A

Loss of ability to carry out learned purposeful tasks

343
Q

What is Agnosia?

A

Loss of ability to recognise objects/people etc

344
Q

Which tumour is ventricular, and associated with hydrocephalus?

A

Ependyoma

345
Q

Which brain tumour is indolent, and common in children?

A

Pilocytic Astrocytoma

346
Q

Which brain tumour is soft, gelatinous and calcified?

A

Oligodendroma

347
Q

Which cause of pneumonia is associated with birds?

A

Chlamydia psittaci

348
Q

How do you distinguish between GBS and Botulism?

A

Descending paralysis in botulism

349
Q

Which bacteria is caught through reheated meats, causes diarrhoea and cramps and may cause gas gangrene?

A

Clostridium perfringens

350
Q

Which bacteria commonly causes infantile diarrhoea?

A

EPEC

351
Q

Which lysosomal disorder occurs due to a defect in Hexoaminidase A, and leads to lipid accumulation, nervous damage and death at a young age?

A

Tay-Sachs Disease

352
Q

Which disorder occurs due to a buildup in Gal-1-phosphate, and leads to cataracts, hypoglycaemia, and neonatal conjugated jaundice?

A

Galactossaemia

353
Q

Which group of disorders (and name 1 example) cause hypoglycaemia, lactic acidosis, hepatomegaly and developmental delay?

A

Glycogen Storage Disorders

Von Gierke’s

354
Q

Name two examples of aminoacidopathies, which present with mental retardation, blue eyes and fair hair/skin.

A

Phenylketonuria

Maple Syrup Disease

355
Q

How does the classical pathway work?

A

C1 binds to antibody-antigen complex

356
Q

How does the mannose binding pathway work?

A

MBL binds to microbial cell surface carbohydrates, which stimulates C2/4 of the classical pathway

357
Q

How does the alternate pathway work?

A

C3 binds straight to the bacterial cell wall

358
Q

Complement: Normal C3, C4, CH50, low AP50?

A

Factor B Deficiency

359
Q

Complement: Normal C3/C4, Low CH50, normal AP50?

A

C2/C1q deficiency

360
Q

Complement: Normal C3/C4, Low CH50/AP50?

A

C9 Deficiency

361
Q

Complement: Low C3/C4, Low CH50, Normal AP50?

A

SLE

362
Q

Monogenic Autoinflammatory?

A

FMF

TRAPS

363
Q

Polygenic Autoinflammatory?

A

IBD
Osteoarthritis
GCA
Takasayu’s

364
Q

Mixed Pattern Diseases?

A

Ankylosing Spondylitis
Psoriatic Arthritis
Behcet’s Syndrome

365
Q

Polygenic Autoimmune Diseases?

A
RA
MG
PA
Graves'
SLE
PBC
Vasculitides
Goodpasture's
366
Q

Monogenic Auto-immune Disease?

A

APS-1
APECED
IPEX
ALPS

367
Q

What do you do to assess allergies if a patient cannot stop anti-histamines or has a history of anaphylaxis?

A

RAST testing

368
Q

What are component resolved diagnostics?

A

Assessment of individual allergen, eg. peanuts have 5 allergens in, this would assess just one of the compounds

369
Q

Which antibody is implicated in Autoimmune Haemolytic Anaemia?

A

Anti-Rh Blood group Antigen

370
Q

Why doesn’t vaccination work properly in the elderly?

A

Immune Senescence

Nutrition

371
Q

Which cells may have potential to be utilised as cancer vaccines?

A

Dendritic Cells

372
Q

For which diseases might you use Interferon Alpha?

A

Hep B/C

CML

373
Q

For which disease might you use Interferon Beta?

A

Behcet’s

374
Q

How does cyclophosphamide work?

A

Alkylates guanine in B cells, preventing replication. Used for vasculitides.

375
Q

How does Azathioprine work?

A

Antimetabolite T>B cells. Prevents cell replication

376
Q

How does Methotrexate work?

A

Anti-folate = anti-proliferation.

377
Q

How does Mycophenolate Motefil work?

A

Anti Metabolite T>B

Used in transplantation prophylaxis

378
Q

How do Tacrolimus/Cyclosporin work?

A

Calcineurin Inhibition = no cell signalling.
T
Rejection prophylaxis

379
Q

What does Sirolimus target?

A

IL-2

Transplant

380
Q

What does Basiliximab target?

A

CD-25

Transplant

381
Q

What does Natalizumab target?

A

Anti-alpha4 integrin

MS

382
Q

What does Tocilizumab Target?

A

IL-6

383
Q

How does transplantation affect the risk of MI?

A

20x increase

384
Q

How does transplantation affect the risk of viral associated cancers?

A

100x increase

385
Q

How does transplantation affect the risk of skin cancer?

A

20x increase

386
Q

What do T Helper 1 cells do?

A

Help CD8/Macrophages

387
Q

What do T Helper 2 cells do?

A

Humoral Response

388
Q

What do T Helper 17 cells do?

A

Help Neutrophils

389
Q

Give an example of a passive vaccination.

A

Varicella Zoster Immunoglobulin

390
Q

Which immunohisto stain targets lymphoid cells?

A

CD45

391
Q

Which immunohisto stain targets epithelial cells?

A

Cytokeratin

392
Q

Which cells form the fibrous cap in the process of artherosclerosis?

A

Vascular smooth muscle

393
Q

Which condition shows ‘myocyte loss with fibrofatty replacement typically affecting the right ventricle’?

A

Arrhythmogenic Right Ventricular Cardiomyopathy

394
Q

Why does Rheumatic Fever occur?

A

Antigenic Mimicry

395
Q

What are Jones’ major Criteria for Rheumatic Fever?

A
Carditis
Arthritis
Sydenham's Chorea
Erythema Marginatum
Subcutaneous Nodules
396
Q

A middle-aged woman presents with shortness of breath and chest pains. O/E she has a mid systolic click with a late systolic murmur. What is the most likely diagnosis?

A

Mitral Valve Prolapse

397
Q

What is the most common cause of Aortic Stenosis?

A

Calcification

398
Q

What is the most common cause of Mitral Stenosis?

A

Rheumatic Fever

399
Q

In which condition might you see ‘Smiling Face’ cells with ‘fish mouths’?

A

Hereditary Stomatocytosis

400
Q

Which type of anaemia is commonly seen in Sideroblastic Anaemia?

A

Microcytic

401
Q

What causes anaemia of chronic disease?

A

Cytokine driven inhibition of red cell production, with increased ferritin.

402
Q

What causes anaemia of chronic disease in renal failure?

A

EPO Deficiency

403
Q

When is TIBC raised?

A

Pregnancy

Iron Deficiency Anaemia

404
Q

How is transferrin saturation calculated, and what can it indicate?

A

Iron/TIBC

<20% may indicate IDA

405
Q

What does the combination of pancytopaenia and splenomegaly imply?

A

Myelofibrosis

406
Q

Which leukaemia most commonly causes pancytopaenias?

A

Hairy Cell

407
Q

What is the key feature of extravascular haemolytic anaemia?

A

Splenomegaly

408
Q

Which complication commonly occurs in Hereditary Spherocytosis?

A

Gallstones

409
Q

Name one serious complication of Hereditary Elliptocytosis.

A

Hydrops Foetalis

410
Q

What can precipitate an acute G6PD attack, presenting with jaundice, anaemia and heinz bodies and bite cells on blood film?

A

Drugs

Broad Beans

411
Q

In which condition are target cells commonly seen?

A

Sickle Cell Disease

412
Q

How are the types of vWD characterised?

A

1: Low
2: Dysfunctional
3: Absent

413
Q

What is Factor V Leiden?

A

Resistance to Protein C = Thrombosis

414
Q

What would be the target INR for a patient after their first DVT/PE?

A

2.5

415
Q

What would be the target INR for a patient after recurrent DVTs?

A

3.5

416
Q

What do you do if a patient on warfarin presents with an INR of 6?

A

Withhold doses until below 5

417
Q

Which blood components decrease in pregnancy?

A
Hb
HCT
Plt
Factor XI
Protein S
418
Q

How does Binet Staging work?

A
A = <3 lymph nodes
B = >3 lymph nodes
C = Anaemia/Thrombocytopaenia
419
Q

Which type of Burkitt’s lymphoma affects the jaw?

A

Endemic

420
Q

Which disease is associated with Mycosis Fungoides?

A

Cutaneous T-Cell Lymphoma

421
Q

How would you treat Essential Thrombocytopaenia?

A

Anagrelide

422
Q

How would you distinguish Circulatory Overload from Acute Lung Injury (Post transplant)?

A

Signs of Cardiac Failure (Raised JVP/PCWP) in acute lung injury

423
Q

A patient presents with skin depigmentation, nodules, trophic ulcers and nerve thickening. What is the likely diagnosis?

A

Hanson’s Disease

Mycobacterium leprae

424
Q

An immunocompromised patient presents with disseminated TB. What is the most likely diagnosis?

A

Mycobacterium Avium Intracellulare Complex

425
Q

A man from Australia presents with painless nodules which are beginning to ulcer, scar and contract. What is the most likely diagnosis?

A

Mycobacterium ulcerans

426
Q

Name a gram negative cocci that can cause typical Pneumonia.

A

Moraxella cattarrhalis

427
Q

Which bacteria are included in the HACEK group?

A
Haemophilus
Acinetobacter
Cardiobacterium
Eikinella
Kingella
428
Q

What is the most likely cause of secretory diarrhoea in an under 6 year old?

A

Rotavirus

429
Q

How many copies of an organism must be present in urine to diagnose a UTI?

A

> 10^4/ml

430
Q

What is the most common cause of infection in a prosthetic joint?

A

Coagulase negative Staph ie. epidermidis

431
Q

How would a brain abscess present?

A

Signs of SOL

Swinging fevers

432
Q

How is Chlamydia diagnosed?

A

NAAT from urethral swab

433
Q

What is Lympho-Granuloma Venereum?

A

Chlamydia infecting lymph nodes

434
Q

What can cause painful inguinal buboes and genital elephantosis?

A

Lympho-Granuloma Venereum

435
Q

What is the role of Haemagglutinin in Influenza?

A

Viral Entry

436
Q

What is the role of Neuraminidase in Influenza?

A

Cleaves sialic acid for exit of infected cells

437
Q

What is the third line treatment for CMV?

A

Cidofovir

438
Q

Which antivirals can be used for Hep C?

A

N33/4 Protease Inhibitors

439
Q

Which virus causes Measles?

A

Morbillivirus

440
Q

A man who drank some untreated milk presents with an undulant fever that peaks in the evening. What is the most likely diagnosis?

A

Brucellosis

441
Q

A patient presents with a fever and conjunctival haemorrhages a day after going swimming in a river. What is the most likely diagnosis?

A

Leptospirosis

L.interrogans

442
Q

A man presents with painless round black lesions with a rim of oedema, and a mediastinal haemorrhage. What is the most likely diagnosis?

A

Anthrax

443
Q

Which type of drug is Amphotericin?

A

Polyene

444
Q

Which gene is mostly implicated in CJD?

A

129 codon MM

445
Q

What are the different types of Renal Tubular Acidosis?

A
1 = Can't excrete H+
2 = Can't reabsorb bicarbonate
4 = Resistant to aldosterone
446
Q

What are the key features of hypokalaemia?

A

Muscle Weakness
Cardiac Arrhythmias
Polyuria
Polydipsia

447
Q

What can cause a sine wave on ECG?

A

Severe Hyperkalaemia

448
Q

Why is ALP normal in Myeloma?

A

Plasma Cells suppress osteoblasts

449
Q

When is Urobilinogen raised?

A

Pre-Hepatic Jaundice

450
Q

Which porphyria presents with urine colour change (Port Wine) with abdominal pain?

A

Acute Intermittent Porphyria

451
Q

Which porphyria presents with both neurovisceral and cutaneous lesions?

A

Variegate

HCP

452
Q

What is the deficiency causing Acute Intermittent Porphyria?

A

HMB Synthase

453
Q

What do skin lesions look like in porphyrias?

A

Blisters on the back of hands that worsen in the sun.

454
Q

What size does a tumour have to be to be considered a macroprolactinoma?

A

> 10mm

455
Q

What is the mainstay of management for Acromegaly?

A

Transphenoidal Surgery

456
Q

Which Thyroid Disease might display ‘Hurthle Cells’?

A

Hashimoto’s Thyroiditis

457
Q

What is the most likely diagnosis if a patient has a ‘stony hard thyroid’?

A

Riedel’s Thyroiditis

458
Q

Which tumours are seen in MEN1?

A

Pituitary Adenoma
Parathyroid Hyperplasia
Pancreatic Neuroendocrine Tumours

459
Q

Which tumours are seen in MEN2a?

A

Parathyroid Hyperplasia
Phaeochromocytoma
Medullary Thyroid Carcinoma

460
Q

Which tumours are seen in MEN2b?

A

Phaeochromocytoma
Medullary Thyroid Carcinoma
Neuromas
‘Marfinoid’

461
Q

A patient with AF presents with confusion and states they are ‘seeing yellow’. What is the likely diagnosis?

A

Digoxin Toxicity

462
Q

What is the most common radiolucent cause of nephrolithiasis?

A

Uric Acid

463
Q

What is the most specific enzyme for Acute Pancreatitis?

A

Lipase

464
Q

Which enzyme is raised in Duchenne’s?

A

Creatine Kinase

465
Q

How long does Troponin remain raised for after an MI?

A

Up to 10 days

466
Q

Which vitamins are commonly deficient in patients with malabsorption syndromes?

A

Fat soluble (ADEK)

467
Q

What causes Farmer’s Lung?

A

Saccharopolyspora rectivirgula

468
Q

What causes Pigeon fancier’s lung?

A

Proteins in excreta/feathers

469
Q

What is the most common cause of IDA in developing countries?

A

Hookworm

470
Q

What is hereditary Pyropikilocytosis?

A

AR condition where erythrocytes are abnormally sensitive to lysis by heat

471
Q

What does Hyxroxycarbimide do?

A

Used in SCD/Myeloproliferative disorders to increase foetal haemoglobin levels

472
Q

In which scenario is transfusion a better treatment for iron deficiency than oral iron?

A

Sepsis and severe infection, as oral iron won’t absorb well.

473
Q

How is Pyridoxine (B6) used as a medication?

A

It promotes RBC production, can be used in disorders with ineffective erythropoiesis such as Sideroblastic Anaemia

474
Q

What would you see on iron studies of a pregnant lady?

A

High Iron
High TIBC
Normal Ferritin

475
Q

Which investigation is most likely to provide a definitive diagnosis in a patient with pancytopaenia?

A

Bone Marrow Biopsy

476
Q

How is B12 deficiency treated?

A

Hydroxocobalamin

477
Q

When must folic acid replacement not be given?

A

If the cause of the deficiency is unknown, as this may exacerbate the neuropathy of B12 deficiency

478
Q

Which enzyme might be raised in Haemolytic Anaemias?

A

Lactate Dehydrogenase

479
Q

When might haptoglobin be low, and why?

A

Intravascular Haemolytic Anaemia, since it binds free haemoglobin

480
Q

Which enzyme deficiencies might cause a Haemolytic Anaemia?

A

Glucose-6-Phosphate Dehydrogenase Deficiency

Pyruvate Kinase Deficiency

481
Q

How is G6PD Deficiency inherited?

A

X-Linked

482
Q

When would you investigate G6PD Deficiency?

A

2-3m after a crisis with an enzyme assay

483
Q

How is Pyruvate Kinase Deficiency inherited?

A

Autosomal Recessive

484
Q

How is Sickle Cell Disease inherited?

A

Autosomal Recessive

485
Q

How is HbA made up?

A

2x Alpha

2x Beta

486
Q

How is HbA2 made up?

A

2x Alpha

2x Gamma

487
Q

How is HbF made up?

A

2x Alpha

2x Delta

488
Q

in which condition might you see a classical ‘hairs on end’ skull X-Ray?

A

Beta-Thalassaemia

489
Q

What is Paroxysmal Cold Haemoglobulinaemia?

A

Hb in the urine caused by a viral infection. Donath-Landsteiner Antibodies stick to Abs in the cold, and complement attacks RBCs as you warm up, leading to haemolysis.

490
Q

How are warm autoimmune haemolytic anaemia and cold agglutinin disease distinguished?

A

Warm: IgG, Spherocytes
Cold: Raynaud’s, IgM

491
Q

How is TTP treated?

A

Emergency plasma exchange

492
Q

What is the pentad of TTP?

A
MAHA
Fever
Renal Impairment
Neurological Abnormalities
Thrombocytopaenia
493
Q

What is paroxysmal nocturnal haemoglobulinuria?

A

Chronic intravascular haemolysis at night due to complement-mediated lysis. Cause morninghaematuria and thrombosis

494
Q

How do you diagnose Paroxysmal Nocturnal haemoglobulinuria?

A

Ham’s Test

495
Q

What is the difference between Acute and Chronic ITP?

A
Acute = Children, self limiting
Chronic = Adults, long-term
496
Q

Which factor is low in vWD?

A

Factor 8

497
Q

Why might you continue LMWH when starting warfarin?

A

Warfarin is initially procoagulant due to Protein C/S deficiency

498
Q

What does Heparin potentiate?

A

Antithrombin III

499
Q

When is Vitamin K indicated?

A

INR over 5 and bleeding

INR over 8 and not bleeding

500
Q

When is prothrombin complex concentrate indicated?

A

Major bleeding

Intracranial haemorrhage

501
Q

When should Anti-D be given to Rh-ve mothers?

A

28 weeks
Sensitising Events
At delivery if baby is Rh+ve

502
Q

In which CML phase are there <5% blasts?

A

Chronic

503
Q

What is the difference between CLL and SLL?

A
SLL = LNs
CLL = BM
504
Q

Which NHLs are B Cell Lymphomas?

A
Burkitt's 
Mantle Cell
MALT
DLBC
Follicular
505
Q

In which lymphoma might you see a ‘nodular/follicular appearance’?

A

Follicular

506
Q

In which lymphoma might you see ‘angular/clefted nuclei’?

A

Mantle Cell

507
Q

Which T Cell lymphoma is most aggressive?

A

Anaplastic

508
Q

Which agent can be used in the management of T Cell Lymphomas/

A

Alemtuzumab

509
Q

What is smouldering myeloma?

A

> 10% clonal plasma cells, but no CRAB symptoms

510
Q

How are AML and myelodysplastic syndromes distinguished?

A

<20% blasts in Myelodysplastic syndromes

511
Q

What are Pelger-Huet Cells?

A

Right shifted hyposegmented neutrophils seen in MDS

512
Q

What is Dyskeratosis Congenita?

A

X-Linked Aplastic Anaemia

Triad of skin pigmentation, nail dystrophy and oral leukoplakia

513
Q

What causes Psuedopolycythaemia?

A

Normal Hb, reduced plasma volume, often due to burns, dehydration and diarrhoea

514
Q

Which conditions are associated with Massive Splenomegaly?

A

Myelofibrosis

CML

515
Q

What is Essential Thrombocytosis?

A

MPD where megakaryocytes dominate the bone marroow

516
Q

What might increase the risk of a patient experiencing anaphylaxis due to a transfusion?

A

IgA Deficiency

517
Q

What mediates ABO incompatiblity?

A

IgM

518
Q

What is a Gohn Focus?

A

Primary latent TB lesion

519
Q

What does BCG stand for?

A

Bacille-Calmette-Guerin

520
Q

Name a gram negative rod that causes typical pneumonia.

A

Klebsiella pneumoniae

521
Q

Name a gram +ve diplococci that causes pneumonia

A

Streptococcus pneumoniae

522
Q

Name a gram -ve cocco-bacilli that causes typical pneumonia.

A

Haemophilus influenzae

523
Q

Name a gram +ve cocci that grows in ‘grape-bunch clusters’ that causes pneumonia.

A

Staphylococcus aureus

524
Q

What is the CURB 65 score?

A
Pneumonia Severity
Confusion
Urea >7
RR >30
BP <90/60
>65yo
525
Q

What is more likely to be seen in subacute than acute IE?

A

Signs O/E such as Osler’s Nodes, Roth spots, janeway lesions and splinter haemorrhages

526
Q

What are the major criteria of the Duke’s Score?

A

New Murmur

2x blood cultures

527
Q

What might cause cellulitis in shellfish handlers?

A

Vibrio vulnificus

528
Q

Which antibiotics most commonly cause pseudomembranous colitis?

A

Ciprofloxacin
Cephalosporins
Clindamycin

529
Q

What is secondary syphylis?

A

Rash and genital warts 1-6m after infection

530
Q

What is tertiary syphylis?

A

2-3y after infection
Granulomas
Dementia
Cardiac Disease

531
Q

How is syphylis investigated?

A

Dark-ground microscopy

532
Q

What causes beefy red ulcers and donovan bodies?

A

Donovanosis (Granuloma Inguinale)

533
Q

Which condition is associated with a whiff test and clue cells?

A

BV

534
Q

What causes Molluscum Contagiousm?

A

Poxvirus

535
Q

Which antibiotic classes target Cell Walls?

A

Beta Lactams

Glycopeptides

536
Q

Which antibiotic classes target protein synthesis?

A
Aminoglycosides
Tetracyclines
Macrolides
Chloramphenicol
Oxazolidinones
537
Q

Which antibiotic classes target DNA synthesis?

A

Fluoroquinolones

Nitroimidazoles

538
Q

Which antibiotics target RNSA Synthesis?

A

Rifamycin

539
Q

Which antibiotics are cell membrane toxins?

A

Polymyxin

Cyclic Lipopeptides

540
Q

Which Antibiotics target folate metabolism?

A

Sulfonamides

Diaminopyrimidines

541
Q

What are the BEAT mechanisms of antibiotic resistance?

A
Bypass antibiotic-sensitive step (MRSA)
Enzyme-mediated inactivation (Beta Lactamase)
Accumulation impairment (Tetracycline)
Target Modification (Quinolone)
542
Q

What causes Kaposi’s Sarcoma?

A

HHV8

543
Q

Which viruses aren’t dsDNA viruses?

A

Hepatitis
MMR
Parvovirus B19

544
Q

Which hepatitis is always a coinfection?

A

Hep D

with B

545
Q

Which Hepatitis is usually a self-limiting, mild infeciton, but may cause severe disease in pregnancy?

A

Hepatitis A

546
Q

Which virus, when caught antenatally, may lead to severe congenital microcephaly and skull deformities?

A

Zika

547
Q

Which antibodies are positive in Hep B vaccination?

A

Anti-HBs

548
Q

Which antibodies are present in previous Hep B infection?

A

Anti-HBs

Anti-HBc

549
Q

Which antibodies are present in chronic Hep B infection?

A

HBsAg

Anti-HBc

550
Q

How is Dengue spread?

A

Flavivirus by Aedes Mosquito

551
Q

Which disease might cause dry gangrene, swollen lymph nodes and is spread by fleas?

A

Plague (Yersinia Pestis)

552
Q

Which disease causes disfiguirng dermal disease in a malnourished child?

A

Visceral Lesihamania (Kala Azar)

553
Q

What does a high Osmolar gap imply?

A

Unmeasured solutes in the serum (toxins etc)

554
Q

What does ALP stand for?

A

Alkaline Phosphatase

555
Q

What does AST stand for?

A

Aspartate Aminotransferase

556
Q

What does ALT stand for?

A

Alanine Aminotransferase

557
Q

Which LFT result is characteristic of Alcoholic Liver Disease?

A

2:1 AST:ALT

558
Q

Which LFT result is characteristic of Viral hepatitis?

A

1:1 AST:ALT

559
Q

Which LFT result is characteristic of Chronic Liver Disease?

A

ALT>AST

560
Q

What might cause a urea 10x higher than usual?

A

Upper GI Bleed

AKI (urea secreted renally)

561
Q

When are pale stools/dark urine seen?

A

Post-hepatic jaundice

562
Q

What stimulates ACTH release?

A

CRH

563
Q

Which hormones are given in a combined pituitary test?

A
Insulin
TRH
LHRH
Normal = Adequate increase in related hormones. 
Abnormal = Hypopituitarism
564
Q

In which condition might you have a raised Aldosterone:Renin ratio?

A

Conn’s

565
Q

What is activated vitamin D called?

A

Calcitriol

566
Q

What are the types of activated vitamin D used as medication?

A

Ergocalciferol (Plants, C2)

Cholecalciferol (Animals, C3)

567
Q

Which form of Vitamin D is stored and measured?

A

25-hydroxy-cholecalciferol
Inactive
Liver

568
Q

When might ALP be pathologically less than 5x higher than normal?

A

Bone Tumours

569
Q

PPV vs Sensitivity

A
PPV = probability it's a true positive
Sensitivity = Probability someone with the disease will.test positive
570
Q

NPV vs Specificty

A
NNV = Probability it's a true negative
Specificity = Probability someone without the disease will correctly test negative
571
Q

Normal GFR?

A

120ml/hr

572
Q

What is Wiskott-Aldrich Syndrome?

A

Eczema
High IgA/IgE
Low IgM
WAS gene mutation

573
Q

What does IPEX (FoxP3) stand for?

A

Immune dysregulation, polyendocrinopathy, enteropathy

574
Q

What does APS 1 (AIRE) stand for?

A

Auto-immune polyendocrine syndrome type 1

575
Q

What does APECED (AIRE) stand for?

A

Auto-immune polyendocrinopathy candidiasis ectodermal dystrophy syndrome

576
Q

What does ALPS (FAS) stand for?

A

Auto-Immune Lymphoproliferative Syndrome

577
Q

What happens in APECED/APS1?

A

Abnormality in T Cell tolerance = multiple autoimmune diseases

578
Q

What happens in ALPS?

A

Abnormality in lymphocyte apoptosis = High WCC and lymphomas

579
Q

What happens in IPEX?

A

Abnormality in T Regulatory Cells leads to diarrhoea, dermatitis and dementia

580
Q

Name two genetic polymorphisms associated with polygenic auto-immune diseases.

A
PTPN22 = RA, SLE, T1DM
CTLA4 = SLE/T1DM/Autoimmune Thyroiditis
581
Q

Which HLA is associated with Pernicious Anaemia and Hashimoto’s Thyroiditis?

A

DR5

582
Q

Which HLA is associated with Haemochromatosis?

A

A3

583
Q

What is serum sickness?

A

Reaction to proteins in penicillin

T3HS

584
Q

Which hypersensitivity type is Chronic urticaria?

A

Type 2

585
Q

Which antibody is associated with mixed connective tissue diseases?

A

Anti-U1RNP (speckled pattern)

586
Q

What does Anti-jo1 target?

A

t-RNA synthetase

587
Q

What is direct transplant recognition?

A

Donor APC presents antigen to recipient T Cells

588
Q

What is indirect transplant recognition?

A

Recipient APCs present antigens to recipient t Cells

589
Q

What would a typical HAART regimen be?

A

2x NRTI + PI

590
Q

What is injected in the mantoux test?

A

Tuberculin

591
Q

What size induration indicates a positive mantoux test?

A

10mm

592
Q

How many Duke’s minor criteria are needed for diagnosis?

A

5

or 3 if one major

593
Q

Which histological pattern is required for diagnosis of Cryptogenic Fibrosing Alveolitis/Idiopathic Pulmonary Fibrosis?

A

Usual Interstitial Pneumonia (sub-plural honeycomb change in periphery)

594
Q

What is Extrinsic Allergic Alveolitis?

A

Inhaled organic antigens leading to immune-mediated alveolar inflammation
Polypoid Plugs of loose connective tissue

595
Q

What are found in both Juvenile Polyposis and Peutz-Jegher’s Synrome?

A

Hamartomatous Polyps of the Bowel (Non-neoplastic)

596
Q

What is Gardner’s Syndrome?

A

Familial Adenomatous Polyps (APC AD) with extra-GI features (Dental caries, osteomas)

597
Q

What is Lynch Syndrome/HNPCC?

A

Carcinomas in right colon, associated with gynae cancers

598
Q

What stimulates pancreatic exocrine function?

A

Secretin

CCK

599
Q

What is metabolic syndrome?

A
Hyperglycaemia
HTN
Obesity
Dyslipidaemia 
Microalbuminaemia
600
Q

What is Acinar Cell Carcinoma?

A

Cancer of exocrine cells of pancreas

Positive for lipase, trypsin and chymotrypsin

601
Q

What are the zones of a liver lobule?

A
1 = periportal hepatocytes
2 = mid
3 = Perivenular Hepatocytes (liver enzymes)
602
Q

When might you see spotty necrosis?

A

Acute Hepatitis

603
Q

When might you see ‘Piecemeal Necrosis’?

A

Chronic hepatitis

604
Q

What is the critical histological stage linking chronic hepatitis to cirrhosis?

A

Bridging from portal vein to central vein

605
Q

Describe the histopathology of a cirrhotic liver.

A

Hepatocyte Necrosis
Fibrosis
Nodules of regenerating Hepatocytes
Disturbance of vascular architecture

606
Q

How is prognosis calculated in cirrhosis?

A

Modified Child’s Pugh Score

607
Q

What are the factors assessed in the Modified Child Pugh Score?

A
Albumin
Bilirubin
Clotting
Distension 
Encepalopathy
608
Q

How is cirrhosis classified?

A
Micronodular = <3mm = Alcohol/Bile
Macronodular = >3mm = Viral/Wilson's/A1At
609
Q

Which form of NAFLD sis benign and shows mild fatty infiltration?

A

Simple Steatosis

610
Q

Which form of NAFLD shows Steatosis and Hepatitis?

A

NASH

611
Q

Which antibodies are associated with Autoimmune Hepatitis?

A

ANA/Anti-SM

Anti-LKM

612
Q

Which biliary disease shows ‘Onion-Skinning fibrosis’?

A

PSC

613
Q

How is HCC monitored?

A

Alpha-fetoprotein

614
Q

Which stain is used for Alpha-1-antitrypsin deficiency?

A

Periodic Acid Schiff

615
Q

Which procedure may be used to treat Benign Prostatic Hyperplasia?

A

TURP

616
Q

Which testicular tumours don’t arise from Germ Cells?

A
Sertoli cell (Sex Cord)
Leydig Cell (Stroma)
617
Q

Which Renal Cancers have:

a) Nests of epithelium
b) Papillary/Tubulopapillary growth
c) Sheets of large cells with distinct border?

A

a) Clear Cell
b) Papillary
c) Chromophobe

618
Q

Which tumour of the bladder has frond-like growths projecting from the bladder wall which are lined by epithelium?

A

Non-Invasive Papillary Transitional cell carcinoma

619
Q

Which bladder cancer has the most invasive behaviour?

A

Invasive Urothelial Transitional Cell carcinoma

620
Q

What is benign familial haematuria?

A

Thin basement membrane disease = TypeIV collagen, asymptomatic haematuria

621
Q

What does loss of podocyte foot processes indicate?

A

Nephrotic Syndrome

622
Q

What causes Nephrotic Syndrome?

A
Primary = FSGS, MG, MCD
Secondary = Diabetes, Amyloidosis
623
Q

What causes Nephritic Syndrome?

A
Post-Strep
IgA Nephropathy
Rapidly Progressive (Crescentic)
Alport's Syndrome
Thin basement Membrane Disease
624
Q

What might cause Rapidly Progressive Glomerulonephriritis?

A

Goodpastures
Immune complex (SLE, Alport’s)
ANCA (Polyangiitis)

625
Q

Which cause of nephritic syndome shows linear deposition of IgG in the glomerular basement membrane?

A

Goodpasture’s

626
Q

Which cause of nephritic syndromes shows ‘granular IgG deposition’?

A

Immune-Complex mediated

627
Q

which cause of nephritic syndrome shows ‘a lack of immune complex deposition’?

A

Polyangitides

628
Q

What might cause asymptomatic haematuria?

A

Thin basement membrane disease
IgA Nephropathy
Alport Syndrome

629
Q

Which IG is deposited in post-strep glomerulonephritis?

A

IgG

630
Q

A man presents with a fever, rash, haematuria and proteinuira/ He is found to have an eosinophila, and a renal biopsy shows inflammatory infiltrate with tubular injury and granulomas. He recently started a course of NSAIDs. What is the most likely diagnosis?

A

Acute Interstitial Nephritis

631
Q

What is the triad of HUS?

A

MAHA
Thrombocytopaenia
Renal Failure

632
Q

Why might you get a murmur in Polycystic Kidney Disease?

A

Mitral Valve Prolapse

633
Q

In which condition might you see ‘wire-loop capillaries’ and ‘lumpy bumpy granular deposition in the GBM’ on a renal biopsy?

A

Lupus Nephritis

634
Q

In which cancers might you see Psammoma Bodies?

A

Papillary Thyroid

Serous Cystadenoma

635
Q

Which cell type is seen in serous cystadenomas?

A

Columnar Epithelium

636
Q

Which morphology is seen in endometroid ovarian cancer?

A

Tubular Glands

637
Q

Which cancer has a ‘hobnail appearance’?

A

Clear Cell Ovarian

638
Q

Which ovarian cancers secrete B-HCG?

A

Choriocarcinoma

639
Q

Which tumour is associated with Meig’s Syndrome?

A

Fibroma

640
Q

Which ovarian cancer produces Oestrogen?

A

Granulosa-Theca Cell tumour

641
Q

Which ovarian cancer secretes androgens?

A

Sertoli-Leydig Cell

642
Q

How is FIGO staging done?

A
1 = Ovaries
2= Pelvis
3 = Abdomen
4 = Distant
643
Q

How does CIN staging work?

A
1 = lower 1/3 epithelium
2 = Lower 2/3
3 = Full thickness
644
Q

How is Lobular carcinoma in situ identified?

A

Incidentally on Biopsy

645
Q

What are the forms of breast carcinoma in situ?

A

Lobular

Ductal (microcalcification of mammogram)

646
Q

On breast biopsy, you see ducts filled with atypical epithelial cells. What is the likely diagnosis?

A

Carcinoma in situ

647
Q

Which medication targets HER2 in breast cancer?

A

Herceptin

648
Q

Which medication targets ER in breast cancer?

A

Tamoxifen

649
Q

Which breast cancer is associated with BRCA?

A

Basal-Like carcinoma

650
Q

Which territory is most likely occluded if a stroke presents with contralateral leg paresis?

A

ACA

651
Q

Which territory is most likely occluded if a stroke presents with contralateral weakness of face and arm?

A

MCA

652
Q

Which territory is most likely occluded if a stroke presents with contralateral hemianopia/quadrantanopia?

A

PCA

653
Q

Which territory is most likely occluded if a stroke presents with ipsilateral ataxia and horner’s?

A

PICA

654
Q

How does Lewy Body Dementia (ASyn) present?

A

Parkinsonism, fluctuations in cognitive ability and hallucinations

655
Q

What is the main component of Lewy Bodies?

A

Alpha-Synuclein

656
Q

Which proteins are targeted in Multiple Sclerosis?

A

Myelin Basic protein

Proteo-Lipid protein

657
Q

XR features of osteoporosis?

A

None

658
Q

Crystal colours to polarised parallel light?

A
Gout = Yellow
Pseudogout = Blue
659
Q

In which condition are ‘Brown Tumours’ seen?

A

Primary Hyperparathyroidism

660
Q

What causes osteomyelitis in SCD patients?

A

Salmonella spp

661
Q

What causes osteomyelitis in children?

A

Haemophilus influenzae

Group B strep

662
Q

How does osteomyelitis present?

A

Fever, malaise, pain, swelling and tenderness

663
Q

In which condition might you see Heberden’s Nodes and Bouchard’s Nodes?

A

Osteoarthritis

664
Q

What are the x-ray features of Osteoarthritis?

A
LOSS
Loss of joint space
Osteophytes
Subchondral Sclerosis
Subchondral Cysts
665
Q

Which joints are spared in Rheumatoid Arthritis?

A

Distal Interphalanegal Joints

666
Q

Which skin condition has ‘saw-toothing of rete ridges’ on histology?

A

Lichen Planus

667
Q

Which skin condition is IgA mediated?

A

Dermatitis Herpetiformis

668
Q

Which skin condition has a ‘Buckshot Appearance’ on histology?

A

melanoma

669
Q

What is Bowen’s Disease?

A

Flat, red, scaly patches on sun-exposed areas

670
Q

How does Actinic Keratosis look on histology?

A
SPAIN 
Solar elastosis
Parakeratosis
Atypia
Inflammation
Not full thickness
671
Q

What does Bowen’s Disease progress to?

A

Squamous Cell Carcinoma

672
Q

Which skin lesions have a ‘waxy, stuck on appearance’?

A

Seborrhoeic Keratosis

673
Q

A patient presents with sheets of skin detachment, with a positive Nikolsky sign. They recently started a new anti-convulsant. What is the most likely diagnosis?

A

Stevens-Johnson Syndrome

674
Q

How does Pityriasis Rosea present?

A

Salmon pink rash (herald patch) followed by oval macules in a Christmas Tree formation

675
Q

Which disease is associated with a ‘Corkscrew Appearance’ on angiogram?

A

Buerger’s Disease

676
Q

What is the triad of Granulomatosis with Polyangiitis?

A

Saddle Nose
Haemoptysis
Glomerulonephritis

677
Q

Which vasculitis presents with an absent pulse?

A

Takasayu’s Arteritis

678
Q

What can cause AA amyloidosis?

A

RA (and other autoimmune)
TB
Renal Cell carcinoma

679
Q

Which enzyme might be raised in Sarcoidosis?

A

ACE

680
Q

Which blood group is universal for fresh frozen plasma?

A

AB

681
Q

Which tumour is associated with pseudomyxoma peritonei?

A

Mucinous cystadenoma

682
Q

How does ALUM work?

A

Promotes B Cell differentiation

683
Q

Which component of COVID does the vaccine target?

A

Spike Protein

684
Q

Which IL-6 Inhibitor can be used in hypoxic COVID?

A

Tocilizumab

685
Q

What is zanamivir used for?

A

Hepatitis A

686
Q

Which broad spectrum antibiotic is typically given in penicillin-allergic patients?

A

Clarithromycin