Thoracic Infection Flashcards

1
Q

Broad pathologies of the lung

A

In broad terms pathologies of the lung can be divided into two main categories:
Airspace
Interstitial

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2
Q

Locational features which may aid the diagnosis of lung infections

A

Community acquired infections tend to cause diffuse filling of airspaces and as such result in lobar consolidation. Nodular pattern is more commonly seen in TB. Peri-hilar distribution is seen in opportunistic infection.

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3
Q

Features of Opacification vs Consolidation

A

Consolidation: Can see Air Bronchograms

Opacifications: Cannot

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4
Q

Features of PCP on CXR

A

PCP

PCP is a disease which involves the interstitium and airspace and is often complicated by lung cysts. As a consequence, PCP has many patterns of abnormality on the CXR which reflects these changes.

In this case there are various patterns of abnormality. Rings are likely to be due to lung cysts, lines indicate involvement of the interstitium and diffuse opacification(*) in the middle lobe indicates airspace disease.

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5
Q

Features of a loculated empyema

A

PA CXR demonstrates opacification in the mid right hemithorax. The hilum and vascular marking are clearly seen though this abnormality. This indicates that the abnormality lies outside the lung, probably within the pleura.

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6
Q

Features of Viral Pneumonia

A

There is reticular-nodular opacification in the peripheries of
both mid and lower zones, and a confluent area of opacification in the right mid zone.

The reticular-nodular pattern of abnormality is more typical of an interstitial rather than air space process. Viral pneumonia is one of the infections which can cause both an interstitial and air space disease pattern of abnormality.

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7
Q

Teaching Point

A

Distribution and cavitation

Upper lobe changes - think TB

Cavitation - think TB, staph aureus and gram negative infections

Cavitation and immunosuppressed - think aspergillus

Bilateral and perihilar - think PCP

Nodular - think TB

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8
Q

Features of aspergilloma on CXR and CT

A

In the left lung there is an ill defined mass containing a concentric lucency. Appearance is typical of an aspergilloma.

CT demonstrates multiple nodules with ill defined margins, air crescent formation
and a ground glass halo (*). The appearances are typical of an invasive aspergillosis infection.

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9
Q

Features of Bronchopneumonia

A

The pre-employment chest radiograph demonstrates
assymmetry at the apices, nodules throughout the left upper lobe and lingula and loss of clarity of left heart border. These appearances are consistent with a bronchopneumonia while the upper lobe distribution is typical of TB.

The follow-up demonstrates progression in the changes and cavitation at the apex, confirming bronchopneumonic TB.

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10
Q

Causes of air-space disease

A

Fluid - cardiogenic and non-cardiogenic pulmonary oedema, protein

Pus - pneumonia

Blood - vasculitis, infarction

Cells - malignant (lymphoma, alveolar cell carcinoma) and inflammatory (sarcoid, EAA, eosinophilia, radiation, BOOP)

Protein - alveolar proteinosis

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11
Q

Features of Miliary TB

A

This was a 50 year old male, UK born, Asian patient with a 6 month history of malaise and occasional cough. The patient was otherwise well.

The radiograph demonstrates subtle nodules scattered throughout the lungs particularly in the right mid zone. Similar changes were present on a chest radiograph 4 months previously.

The HRCT demonstrates widespread nodules with a random distribution throughout the lung. There is involvement of both the septae/fissures, pleura, bronchovascular bundles and centrilobular structures.

The diagnosis was milary tuberculosis, HIV positive.

The radiograph appearances are non specific. TB was initially considered, however this seemed unlikely in view of the static nature of the nodules. ‘Random distribution’ of nodules seen on the HRCT is typical of haematogenous spread of tuberculosis.

Milary tuberculosis can occasionally present with an indolent course, as in this case, and is a recognised feature of TB in patients who are HIV positive.

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12
Q
A
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