Childhood and Worker's Diseases Flashcards

1
Q

what is a pleural effusion

A

abnormal collection of fluid in the pleural space

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2
Q

what are the two most useful tests for diagnosing pleural effusion

A

ultrasound and x-ray

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3
Q

what is the appearance of a pleural effusion on an x-ray and what does it suggest

A

flat line suggest pneumothorax or hydro-pneumothorax
round substances in between lobes suggest fluid
meniscus suggest fluid

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4
Q

what is the name for pleural effusions with protein content less than 30mg

A

Transudate

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5
Q

what is the name for pleural effusions with protein content more than 30mg

A

Exudate

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6
Q

what does a straw coloured pleural aspirate suggest

A

cardiac failure, hypoalbuminaema

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7
Q

what does a blood pleural aspirate suggest

A

trauma, malignancy, infection, infarction

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8
Q

what are the causes of transudate effusions

A

heart failure, meigs syndrome, liver cirrhosis

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9
Q

what are the causes of exudate effusions

A

pneumonia, TB, carcinoma,

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10
Q

what is meigs syndrome

A

a triad of benign ovarian tumour, pleural effusion and ascites

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11
Q

what is the normal pleural pH

A

7.6

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12
Q

what does a pleural pH of less than 7.3 suggest

A

pleural inflammation, empyema, malignancy

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13
Q

what is the treatment plan for pleural effusions

A

depends on underlying cause

but can drain the effusion

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14
Q

what is pleurodesis and what is it used as a treatment for

A

artificial procedure to prevent the lung from collapsing again
pleural effusions

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15
Q

what are the related conditions of asbestos

A

benign pleural plaques
diffuse pleural thickening
pleural effusion

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16
Q

what stage of asbestos exposure is asymptomatic

A

benign pleural plaques

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17
Q

what are the symptoms often caused by acute asbestos pleuritis

A

fever, pain, bloody pleural effusions

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18
Q

what do pleural effusions and diffuse pleural thickening cause in patients

A

restrictive impairment

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19
Q

what is malignant mesothelioma

A

incurable pleural cancer

presents with chest pain and pleural effusion

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20
Q

what are the typical features of pulmonary fibrosis related to asbestosis

A

restrictive defect
asbestos bodies in sputum
asbestos fibre in biopsy

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21
Q

what are the two cancers that patients with asbestosis exposure have increased risk to

A

bronchial adenocarcinoma and mesothelioma

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22
Q

what are the clinical features of asbestosis

A

progressive dyspnoea
clubbing
find, end-inspiratory crackles
pleural plaques

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23
Q

what is sarcoidosis

A

a granulomatous (type 4 hypersensitive) disease

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24
Q

symptoms of chronic sarcoidosis

A

lung infiltrates (alveolitis)
skin infiltrates
hypercalcaemia
peripheral lymphadenopathy

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25
Q

signs of sarcoidosis seen on an x-ray

A

bilateral hilar lymphadenopathy

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26
Q

symptoms of acute sarcoidosis

A
erthyema nodosum (red nodules on the legs)
painful joints and eyes
inflammation of the glands
bilateral hilar lymphadenopathy
fever
dry cough
progressive dyspnoea
chest pain
decreased exercise tolerance
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27
Q

differential for bilateral hilar lymphadenopathy on an x-ray

A

sarcoidosis

TB

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28
Q

signs of sarcoidosis seen on a CT-scan

A

peripheral nodular infiltrate

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29
Q

signs of sarcoidosis seen on a tissue biopsy

A

non-caseating granuloma

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30
Q

signs of sarcoidosis in blood tests

A

raised ACE serum levels
raised calcium levels
raised inflammatory markers

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31
Q

Treatment of acute and chronic sarcoidosis

A

Acute - self limiting, NSAIDs, steroids (if vital organ damage)
Chronic - oral steroids, immunosuppresion

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32
Q

buzzwords for sarcoidosis

A
  • African-Carribean woman
  • Raised Ca2+ and ACE levels
  • Bilateral hilar lymphadenopathy, erythema nodosum, granulomas, fatigue, uveitis and weight loss
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33
Q

buzzwords for pleural effusion

A

stony dull to percuss

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34
Q

what is EAA

A

hypersensitive pneumonitis

type III hypersensitive (immune complex deposition)

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35
Q

what are some causes of EAA

A

Bird-fanciers and Pigeon-fanciers lung
Farmer’s and mushroom workers lung
Malt worker’s lung

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36
Q

acute presentation of EAA

A

dry cough, breathlessness, fever, myalgia, no wheeze, crackles, hypoxia

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37
Q

chronic presentation of EAA

A

increasing dyspnoea, weight loss, clubbing, crackles, dry cough

38
Q

what is common of EAA on x-rays

A

upper zone mottling/consolidation

39
Q

what is the results of pulmonary function test in EAA (what type of defect)

A

restrictive defect
low FEV1 and FEV
high or normal ratio
low gas transfer

40
Q

how to diagnosis EAA

A

history of exposure

presence of IgG antibodies to guilty antigen

41
Q

treatment for EAA

A

remove antigen

steroids if needed

42
Q

4 C’s of idiopathic pulmonary fibrosis (IPF)

A

(dry) cough, clubbing, crepitations, cyanosis

43
Q

secondary causes of IPF

A

RA, systemic sclerosis, asbestos, drugs

44
Q

presentation of IPF

A

progressive breathlessness, dry cough, malaise, weight loss, joint pain (arthralgia)

45
Q

PFT of patient with IPF

A
restrictive defect
decreased FEV1 and FVC
normal or raised ratio
reduced lung volumes
low gas transfer
46
Q

X-ray of patient with IPF

A
  • honeycomb lung

- bilateral lower zone reticulonodular shadowing

47
Q

CT scan of IPF

A
  • ground glass appearance
48
Q

treatment of IPF

A

oxygen, opiates, pallative care

recommended high dose steroids not used

49
Q

buzzwords for IPF

A

Ground-glass appearance on X-ray

Honeycomb lung

50
Q

what are the two types of coal worker pneumoconiosis

A

Simple

Complicated

51
Q

what is simple pneumoconiosis

A

chest x-ray abnormality only
no impaired lung function
associated with COPD

52
Q

treatment of simple and complicated pneumoconiosis

A

avoid coal dust
treat co-exisiting chronic bronchitis
claim compensation

53
Q

what is complicated pneumoconiosis

A

progressive massive fibrosis leading to restrictive pattern with breathlessness
associated with emphysema

54
Q

what does complicated pneumoconiosis eventually go on to cause

A

Cor pulmonale

55
Q

what is Caplan’s syndrome

A

association between rheumatoid arthritis, pneumoconiosis and pulmonary rheumatoid nodules

56
Q

what is silicosis

A

simple pneumoconiosis - chest XR abnormality only

57
Q

what is seen in a chest x-ray of silicosis

A

egg-shell calcification of hilar nodes

diffuse miliary or nodular pattern in the upper zone

58
Q

clinical features of silicosis

A

progressive dyspnoea, increased incidence of TB, restrictive tendency

59
Q

buzzwords for silicosis

A
  • Snow storm appearance on x ray

- egg-shell calcification of hilar nodes on x ray

60
Q

what is the pathology of neonatal respiratory distress syndrome

A

not enough surfactant in the lungs to keep them inflated

61
Q

what is in surfactant and what is its production stimulated by

A

phospholipids, apoproteins

steroids

62
Q

what is the complications of neonatal distress syndrome

A

no breath sounds on 1 side

sudden deterioration

63
Q

what is the x-ray appearance of neonatal distress syndrome

A

distinctive cloudy appearance

64
Q

what is the treatment of neonatal distress syndrome

A

ventilation, artificial surfactant

65
Q

buzzwords for neonatal distress syndrome

A

ground glass appearance on x-ray

66
Q

what is a pneumothorax

A

air in the pleural space

67
Q

what can causes a pneumothorax in infants

A

intermittent postive - pressure ventilation

68
Q

what is the classification of chronic lung disease in infants

A

O2 requirements beyond 36 weeks corrected gestation plus evidence of ILD

69
Q

what is indicative of cystic fibrosis

A

infant with raised immune-reactive trypsin levels on neonatal screening

70
Q

what is CF

A

autosomal recessive

mutations in the CF transmembrane conductance regulator (CFTR) gene on chromosome 7

71
Q

what does the defect in CF cause

A

error in Cl- channel leads to defective Cl secretion and increase sodium absorption across airway epithelium

72
Q

what does CF predispose the lungs to

A

chronic pulmonary infections

bronchiectasis

73
Q

clinical features of CF in neonatal

A

failure to thrive
rectal prolapse
loose stool due to meconium ileus (bowel is sticky causes it to block)

74
Q

clinical features of CF in young adult

A
cough, wheeze, recurrent infections
cor pulmonale
male infertility
nasal polyps
gallstones
75
Q

how is CF diagnoses

A

sweat test - sodium and chloride levels > 60mmol/L

genetics - screen for mutatiosn

76
Q

tests for CF

A

bacteriology - cough swab, sputum culture

spirometry - obstructive defect

77
Q

management of CF

A

physiotherapy, bronchodilators

78
Q

what is Kartagener’s syndrome

A

autosomal recessive disease

defect in the structure and function of sensory and motile cilia

79
Q

presentation of Kartagener’s syndrome

A
  • possible neonatal RDS
  • chronic rhinorrhoea, rhinitis, otitis
  • COPD, recurrent pneumonia, bronchiectasis
  • male infertility, decreased female fertility
80
Q

features of Kartagener’s syndrome

A

dextrocardia

81
Q

what is croup

A

viral laryngotracheobronchitis

i.e. infection of the larynx and trachea

82
Q

signs of croup

A

stridor

barking cough

83
Q

treatment for croup

A

oral steroids

84
Q

what is pertussis

A

“whooping cough”

85
Q

baby from developing country, irritable, no fever, neck rigidity

A

mycobacterium TB

86
Q

what is common causes of bronchiolitis in the young

A

Respiratory Syncytial Virus (RSV)
hMPV
adenovirus

87
Q

symptoms of bronchiolitis in the young

A

tachypnoea, poor feeding, irritating cough,

apnoea in small babies

88
Q

symtoms and features of pneumonia in small children

A

cough, sputum, fever

dullness on percussion, increased vocal fremitus and resonance, bronchial breathing

89
Q

microorganisms causing pneumonia in neonates

A

E.coli, Klebsiella, Staph aureus

90
Q

microorganisms causing pneumonia in infants

A

strep pneumonia, chlamydia,

91
Q

microorganisms causing pneumonia at school age

A

strep pneumonia, Staph aureus, legionella, mycoplasma

92
Q

what type of chest pain is worse on inspiration

A

pleuritic