Dermatology/Rheumatology Flashcards

(41 cards)

1
Q

Treatment of bowens disease

A

Topical 5 fluoracil

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2
Q

Treatment of rosacea

A

Topical metronidazole (mild symptoms)
Brimonidine gel
Oxytetracycline orally if severe symptoms

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3
Q

What is the most common cardiac manifestation of lupus?

A

Pericarditis

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4
Q

What antibodies are associated with polymyositis?

A

Anti synthetase antibibodies

Anti Jo 1

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5
Q

Causes of osteomalacia

A
Vitamin D deficiency 
Chronic kidney disease 
Anticonvulsant medications 
Inherited 
Liver cirrhosis
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6
Q

Blood results in osteomalacia

A

Low vitamin D
Low calcium
Low phosphate
Raised alkaline phosphatase

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7
Q

Treatment of osteomalacia

A

Vitamin D supplementation

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8
Q

What is the inheritence pattern of hereditary haemorrhagic telangiesctasia?

A

Autosomal dominant

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9
Q

What are the symptoms of pellagra (niacin deficiency)

A

Dermatitis, diarrhoea and dementia

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10
Q

Treatment of pyoderma gangrenosum?

A

Oral steroids

Ciclosporin/Infliximab in some cases

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11
Q

Blood results in pagets disease?

A

Raised ALP. Normal calcium and phosphate

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12
Q

Treatment for pagets disease

A

Bisphosphonates

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13
Q

What is the most common malignancy associated with acanthosis nigricans

A

Gastrointestinal cancer

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14
Q

What is the gold standard diagnostic investigation for polymyositis?

A

Muscle biopsy

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15
Q

First line treatment for chronic plague psoriasis

A

Topical potent corticosteroid and vitamin D analogue

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16
Q

Antibodies for drug induced lupus?

A

Anti histone antibodies

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17
Q

What are the most common causes of drug induced lupus

A

Procinamide

Hydralazine

18
Q

How does denosumab work?

A

Human monoclonal antibody that prevents the development of osteoclasts by inhibiting RANKL.

19
Q

Antibodies in sjogrens syndrome?

A

Rheumatoid factor
ANA
Anti Ro
Anti LA

20
Q

Which way does the lens dislocate in marfans syndrome?

21
Q

Risk factors for pseudogout

A
Haemochromatosis 
Hyperparathyroidism 
Low magnesium 
Low phosphate 
Acromegaly 
Wilsons disease
22
Q

Type of crystals in pseudogout

A

Calcium pyrophosphate

Weakly positive birefringent rhomboid shaped crystals

23
Q

What is sezary syndrome?

A
T cell cutaenous lymphoma 
Symptoms include itching, erythroderma of the palms, soles and face
Atypical T cells
Lymphadenopathy 
Hepatosplenomegaly
24
Q

Antibodies for diffuse cutaneous systemic sclerosis?

A

SCL 70 antibodies

25
Most common cause of death in diffuse cutaneous systemic sclerosis?
Interstitial lung disease and pulmonary hypertension
26
Antibodies for limited cutaneous systemic sclerosis?
Anti centromere
27
Virus associated with polyarteritis nodosa
Hepatitis B
28
What is necrobiosis lipoidica diabeticorum?
Shiny, painless areas of yellow/red skin on the shins or people with diabetes
29
What is the triad of symptoms in bechets syndrome?
Oral ulcers, genital uclers and anterior uveitis
30
What HLA type is associated with bechets syndrome?
HLA B51
31
Antibodies associated with dermatomyositis?
Anti Mi 2
32
Is microscopic polyangitis more associated with pANCA or c ANCA?
pANCA
33
Antibodies associated with SLE?
``` ANA Rheumatoid factor (20%) ANti DsDNA (highly specific) Anti Smith (highly specific) Anti Ro and Anti La ```
34
Drugs which worsen psoriasis?
Beta blockers, lithium, chlroquine, NSAIDS, ACE inhibitors, infliximab
35
What is pagets disease?
A disease of increased bone turnover.
36
Treatment for methotrexate toxicity?
Folinic acid
37
What is the criteria for TNF inhibitors in rheumatoid arthritis?
Inadequate response to at least two DMARDs including methotrexate
38
What is the most definitive diagnostic test for sjogrens syndrome?
Salivary gland biopsy
39
What are the features of stills disease/
``` Arthralgia Elevated ferritin Pink maculopapular rash Pyrexia Lymphadenopathy RF and ANA negative ```
40
Treatment for stills disease?
NSAIDs Steroids (may improve symptoms but don't improve prognosis) If persisting symptoms methotrexate, IL1 or anti TNF can be considered.
41
Treatment for lichen planus?
Potent topical corticosteroids