Revision: Lung Conditions Flashcards

1
Q

what is sarcoidosis?

A

Multisystem granulomatous (type IV) disorder to an unknown antigen
non caseating

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

who is sarcoidosis seen in?

A

under 50
Afro-Caribbean
Females
less common in smokers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

signs of sarcoidosis?

A
  • Lymphadenopathy (swollen lymph nodes)
  • Crackles on lung auscultation
  • erythema nodosum (shins)
  • bilateral hilar lymphadenopathy- enlarged lymph nodes in chest
  • arthritis
  • uveitis, parotitis
  • fever
  • hypercalcaemia
  • raised serum ACE
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

erythema nodosum

A

sarcoidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

sarcoidosis management?

A

acute- self-limiting/ NSAIDs/ oral steroids e.g. prednisolone if end organ damaged

chronic-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

sarcoidosis management?

A

acute- self-limiting/ NSAIDs/ oral steroids e.g. prednisolone if end organ damaged

chronic- - Oral steroids if end organ damage e.g. lung, eyes, heart, brain (usually needed) e.g. prednisolone
- May need immunosuppression e.g. METHOTREXATE, azathioprine, anti-TNF therapy (1st to 3rd line)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

most common ILD?

A

idiopathic pulmonary fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

signs of idiopathic pulmonary fibrosis?

A
  • Clubbing
  • Cyanosis
  • Bilateral fine INspiratory crackles
  • bilateral infiltrates on CXR
  • ground glass (early), honeycombing (late stage)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

idiopathic pulmonary fibrosis LFTs?

A

restrictive pattern
reduced FV1/ FVC
normal/ raised DEV1/FVC ratio
ow gas transfer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

idiopathic pulmonary fibrosis investigations?

A

HRCT

CXR
PFTs
Lung biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

idiopathic pulmonary fibrosis management?

A
  • Antifibrotic drugs (nintedanib, pirfenidone) - slow progression
  • Oxygen if hypoxic
  • Lung transplant in young patients
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

which type of hypersensitivity id hypersensitivity pneumonitis?

A

type 3
(IgG)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is an antigen for farmer’s lung?

A

thermophilic bacteria

avian proteins- bird fanciers
fungi - malt workers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

which kind of wheeze is in hypersensitivity pneumonitis?

A

no wheeze

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

management of hypersensitivity pneumonitis?

A

antigen avoidance, oxygen, steroids (oral), antifibrotic therapy to slow progression - pirfenidone, nintendanib

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

exposure to quartz, miners?

A

silicosis

16
Q

what is Caplan’s syndrome?

A

caused by occupational dust inhalation in patients with RA (rheumatoid arthritis)

17
Q

management of chronic progressive fibrosis?

A
  • Bronchodilator, ICS
  • Oxygen if required
  • Pulmonary rehab