CPC 3 pleural effusion Flashcards

1
Q

Clinical examination findings suggesting pleural effusion

A
Dull percussion
Decreased vocal fremitus
Decreased breath sounds
Decreased vocal resonance. 
Asymmetrical decreased chest expansion.
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2
Q

Mechanisms for the formation of pleural fluid

A
Increase hydrostatic
pressure
 Decreased oncotic
pressure
 Increased permeability
of pleura
 Increased pulmonary
interstitial fluid
 Movement from other
cavities (peritoneal)
 Vascular rupture into thorax
 Rupture of thoracic duct
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3
Q

Does cardiac failure cause right, left or bilateral pleural effusions?

A

Any of the above, though equal ones are slightly more common.

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4
Q

What are the BTS guidelines for how to manage a pleural effusion?

A

Take a history, clinical examination and CXR. If a transudative causes is likely from the clinical picture, then treat the cause. If not, or if treatment is unsuccessful, refer to a chest physician.

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5
Q

What are Light’s criteria to diagnose exudative pleural fluid?

A

Pleural fluid is an exudate if one or more of the following
criteria are met:
 Pleural fluid protein divided by serum protein is >0.5
 Pleural fluid lactate dehydrogenase (LDH) divided by
serum LDH is >0.6
 Pleural fluid LDH >2/3 the upper limits of laboratory
normal value for serum LDH.

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6
Q

Basic rule of thumb to differentiate an exudative from a transudative pleural fluid.

A

Pleural fluid protein >30 g/l has indicated an exudate and

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7
Q

Common causes of exudative pleural fluid.

A

Parapneumonic effusions,

Malignancy.

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8
Q

Causes of transudative pleural fluid.

A
All the failures: 
LVF
liver failure (cirrhotic disease), hypoalbuminaemia and peritoneal dialysis. 
nephrotic syndrome
hypothyroidism. 

Also:
PE
mitral stenosis
constrictive pericarditis.

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9
Q

If pleural fluid has NT-proBNP level of >1500, what does this mean?

A

Suggests cause of transudative effusion is cardiac failure.

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10
Q

What does a pleural fluid pH

A

Malignant effusion, pleural infection, connective tissue disorder esp rheumatoid arthritis, TB or oesophageal rupture.

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11
Q

If pleural fluid glucose is low what is likely to be the cause?

A

Infection, arthritis or cancer:
complicated parapneumonic
effusions, empyema, rheumatoid pleuritis and pleural effusions
associated with TB, malignancy and oesophageal rupture

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12
Q

Pleural amylase can be useful when?

A

in suspected cases of oesophageal rupture or effusions associated with pancreatic diseases.

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13
Q

Microbiology of community acquired pneumonia

A

Strep spp are more than half.

The rest are Staph aureus, enterobacteriaceae, or anaerobes.

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14
Q

Microbiology of HAP

A

Staph (25% MRSA)
Gram neg aerobes e.g. E. coli, Pseudomonas and Klebsiella.
Anaerobes.

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15
Q

Routes by which bacteria can enter the pleural space.

A

1) Across the pleura from the adjacent lung.
2) Via visceral pleural defects of fistulae e.g. in cancer, necrotising pneumonia etc.
3) Haematogenous spread
4) Penetrating injury
5) Spread from mediastinum e.g. oesophageal rupture.
6) Across the diaphragm.

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16
Q

Neutrophils in pleural fluid suggest what condition?

A

Underlying pneumonia.

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17
Q

Frank pus in pleural fluid suggests what condition?

A

Empyema

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18
Q

What cells in pleural fluid can mimic malignancy?

A

Reactive mesothelial cells.

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19
Q

Eosinophils in pleural fluid suggest what condition?

A

Pneumothorax or haemothorax. Rarely, drug reactions, parasitic infection, pulmonary infection, or Churg-Strauss syndrome.

20
Q

Lymphocytes in pleural fluid suggest what condition?

A

Inflammatory disease such as RA,
Infection, including mycobacterial,
Malignancy,
previous CABG.

21
Q

Usual imaging on presentation of mesothelioma.

A

Nodular or extensive pleural thickening, large unilateral pleural effusion, contraction of affected hemithorax,
invasion of surrounding structures,
focal pleural plaques.

22
Q

CT features of an empyema

A
 Lenticular shape
 Uniform enhancing wall
 Compression of adjacent lung
 Obtuse angle with chest wall
 ‘Split pleura’-separation of pleural layers
 May have air fluid level
23
Q

Pleural tumours other than malignant mesothelioma

A

Mesenchymal including sarcoma

Lymphoma

24
Q

Usual presentation of mesothelioma

A

Chest pain and dyspnoea

Bloody pleural effusion

25
Q

Progress of malignant mesothelioma.

A

 May be locally invasive (similar to lung
cancer)
 Nodules –> plaques –> encase lung
 Metastasises to nodes and distant sites late

26
Q

Tissue diagnosis of mesothelioma requires…

A

Targeted needle biopsy or thoracoscopic biopsy

May need repeated attempt to get confirmation

27
Q

Histological types of mesothelioma

A

 Epithelioid
 Sarcomatoid
 Biphasic
 Desmoplastic

28
Q

Prognosis of mesothelioma.

A

94% die within 2 years of onset of symptoms
 Median survival 10 months
 Prognosis for epithelioid subtype slightly
better than for sarcomatoid or biphasic types

29
Q

Benign lung tumours

A

Hamartoma.

30
Q

Definition of hamartoma.

A

A tumour formed of mature
but disorganised elements normally found at
that site.

31
Q

Key points about a hamartoma.

A
 Circumscribed peripheral ‘coin’ lesion
 Symptomless, incidental
 Composed of cartilage, epithelium and connective
tissue
 No malignant potential
32
Q

Factors predisposing to lung cancer.

A
SMOKING!!!
Urban living
Asbestos
Radon gas
Radiotherapy
33
Q

Basic division of lung cancers

A

Non-small cell
Endocrine
Rarities

34
Q

Types of non-small cell lung cancer.

A

Adenocarcinoma (common in non-smokers)
Squamous cell carcinoma (nearly half all lung cancers),
Large cell undifferentiated

35
Q

Types of lung endocrine tumour

A
Small cell (metastasises early). 
Large cell neuroendocrine
Carcinoid (typical and atypical, NOT related to smoking.)
36
Q

What age do people present with carcinoid lung cancers? Which type has a better prognosis.

A

Mean of 50 yrs.

Typical.

37
Q

Is carcinoid lung cancer common?

A

No, it makes up less than 1% of lung cancers.

38
Q

Complications of carcinoid lung cancers.

A

Bronchial obstruction inc distal collapse, bronchiectasis or pneumonia.
Haemoptysis

39
Q

Key points about small cell lung cancer (endocrine)

A

Approx 16% of lung cancer
 Metastasises early
 Mediastinal lymph nodes often larger than
primary lung tumour

40
Q

Prognosis for small cell lung cancer (endocrine)

A
Chemotherapy is the main treatment
 Only rarely operable
Prognosis is poor
 Approx 3 months untreated
 1-2 years with chemo
41
Q

Key points of squamous cell carcinoma (non-small cell)

A
40-50% lung cancer and falling
 Arises on a main or segmental bronchus
 May cavitate
 Often directly invades hilar lymph nodes but
metastasises late
42
Q

Precursor lesion for squamous cell carcinoma.

A

 squamous metaplasia
 squamous dysplasia
 carcinoma in situ

43
Q

Key points for adenocarcinoma

A
 20-30% of lung cancer and rising proportion
 Female predilection
 Lung cancer in non-smokers often
adenocarcinoma
 May be central or peripheral
44
Q

Precursor lesions for adenocarcinomas

A

 Atypical adenomatous hyperplasia

 Adenocarcinoma in situ (‘lepidic’)

45
Q

Key points of large cell carcinoma

A

Crosses the non-small cell/endocrine divide.
 10-20% lung cancer
 No evidence of squamous or glandular
differentiation
 Variety of subgroups
 Large cell neuroendocrine carcinoma best known
 Usually aggressive tumours

46
Q

Spread of lung cancer: local, lymph and distant

A

Local: any local structure - if symp chain involved, Pancoast’s. Can also spread to recurrent laryngeal nerve or phrenic nerve.
Lymph: Hilum of lung then mediastinal and supraclavicular. Later, neck and abdominal nodes.
Distant: liver, brain, adrenal, bone, kidney, contralateral lung.

47
Q

Staging of tumours

A
T = how big, how much invaded, how far from carina?
N = lymphnodes, ipsi or contra.
M = contralateral lung, malignant pleural effusion, distant.