Lecture 9 Interstitial Lung Disease Flashcards

1
Q

Interstitial lung disease (ILD):

____ lung expansion causes _____ lung volumes; ie ____ FVC and TLC. What is the FEV1/FVC ratio?

A

reduced, reduced;
reduced;
greater than 80% (FEV doesn’t decrease as much as FVC)

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2
Q

most common cause of ILD

A

idiopathic pulmonary fibrosis (IPF) aka usual interstitial pneumonia (UIP)

different names for same thing

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3
Q

IPF is (reversible or irreversible); does it respond to treatment? Does stopping smoking help?

A

irreversible; not really, will need lung transplant;

no

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4
Q

IPF is characterized by an insidious ____ ____ that is disabling over time. the cough is (productive or nonproductive). seen in (older or younger patients?

A

exertional dyspnea, non productive; older

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5
Q
classic clinical picture of IPF:
unilateral or bilateral crackles?
Subpleural or pleural?
apices or bases?
characteristic \_\_\_\_\_
\_\_\_\_ abnormality
A
bilateral;
subpleural
bases
honeycombing
reticular
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6
Q

peripheral traction ____ may occur in IPF

A

bronchiectasis

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7
Q

what is the 6MWT?

A

6 minute walk test–monitors IPF progression

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8
Q

2 drugs that have shown promise in treating IPF

A

pirfenidone, nintedanib

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9
Q

nonspecific interstitial pneumonia (NSIP):

seen in ____ patients that smoke. there is tachypnea, crackles, but no ____ ____

A

younger; digital clubbing (as opposed to IPF)

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10
Q

NSIP shows a characteristic _____ finding on CT. It is typically __lateral and located in the ____ of the lungs

A

ground glass;

bi, base

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11
Q

Acute Interstitial Pneumonia (AIP)/Hamman-Rich causes _____ alveolar damage. it mainly affects ____ patients that ____. what is the prognosis?

A

diffuse, younger, smoke;

“bad”

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12
Q

respiratory bronchiolitis associated ILD (RB-ILD) is seen in patients with a history of ____ smoking. Patients are typically ____ and have (lot of symptoms or few symptoms?)

A

heavy, younger, few

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13
Q

RB-ILD is characterized by bibasilar end ____ ______ and diffuse centrilobar ____ opacities

A

inspiratory crepiations;

ground glass

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14
Q

Desquamative interstitial pneumonia is seen predominantly in _____ patients that _____. The course is characterized as _____ cough and dyspnea. What is the prognosis>?

A

younger, smoke;
insidious/subacute;
“better”

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15
Q

lymphocytic interstitial pneumonia (LIP) is characterized by monotonous sheets of ___ clonal lymphocytes. it is associated with what 2 diseases?

A

poly;

AIDS, sjogren’s

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16
Q

besides IPF, do all interstitial pneumonias improve with immunosuppression or smoking cessation?

A

you betcha

17
Q

cryptogenic organizing pneumonia is characterized by bilateral air-space ____ or ground glass opacities. There is bronchial ___ thickening or _____ in abnormal areas. It has a good prognosis with _____.

A

consolidation; wall, dilatation;

steroids

18
Q

acute vs chronic eosinophilic pneumonia:
which has eiosinophilia in the lungs? which has it in the blood?
which is more likely to relapse?

A

both, chronic in the blood;

chronic

19
Q

sarcoidosis causes _____ granulomas. it causes bilateral enlargement of ____ lymph nodes. what classic skin finding is seen with it?

A
non-caseating; hilar (and mediastinal);
erythema nodosum (on shins).

“lymphocytic distribution”

20
Q

other symptoms of sarcoid in include ____, hyper____, and CNS involvement

A

uveitis, calcemia

21
Q

histiocytosis X (langerhans) is a disorder characterized by accumulation of _____ ____ in various organs. causes ____ lesions on X ray with a ____ body in the cytoplasm of cells

A

mononuclear phagocytes;
cystic;
birbeck (X-body)

22
Q

treatment of histiocytosis X:

A

stop smoking

23
Q

classic triad of wegener’s granulomatosis: necrotizing ____, ____, and _____
what kind of anca is seen?

A

vasculitis, granulomas in the lung/upper airway, glomerulonephritis;
c-anca

24
Q

large ____ densities, sometimes causing ____, are seen on CXR in patients with Wegener’s. treatment is what?

A

nodular, cavitations;

corticosteroids, cyclophosphamide

25
Q

hypersensitivity pneumonitis: classically due to exposure of _____. BAL shows lavage fluid _____.

A

bird droppings/birds (allergen)

lymphocytosis

26
Q

lymphangioleimyomatosis (LAM) is seen in ____ women that present with _____ or pneumothorax. what kind of lesions are seen in the lung?

A

young, dyspnea;

cystic

27
Q

4 drugs listed in FA that can cause interstitial lung disease:

A

bleomycin, busulfan, amiodarone, methotrexate

28
Q

what happens to diffusion capacity in patients with ILD?

A

its going down (it decreases)

29
Q

which 2 general conditions can cause interstitial shadowing on a CXR? how do you differentiate between the 2?

A

cardiogenic pulmonary edema responds to lasix;

ILD does not

30
Q

does ILD usually cause pleural effusion?

A

no

31
Q

what condition causes pleural thickening>?

A

asbestosis