Interstitial Lung Disease CIS I Flashcards

(36 cards)

1
Q

75yo M abnormal CXR, 60py tobacco, myalgias in shoulder and neck, fatigue, sinus infection, hemoptysis, weight loss, T 99F, crackles b/l, b/l lung nodules - cavitated, WBC 10,000

A

most likely diagnosis

-wegners granulomatosis

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2
Q

wegners granulomatosis

A

sinusitis
lung
kidney

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3
Q

DDx for cavitary lung lesions

A

CAVITY

c - carcinoma
a - autoimmune - wegners
v - vascular
i - infection 9 TB, fungal, bacterial
t - trauma
y - young - congenital lesions
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4
Q

61yo M increasing SOB last year, hacking non-prod cough, a-fib, HTN, rheumatoid arthritis, velcro-like crackles, split S2, pitting lower extremity edema, clubbing

FVC 50%, FEV1 50%, FEV1/FVC 98%

A

appropriate next step in management

-stop amiodarone and methotrexate

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5
Q

amiodarine and methotrexate

A

can cause restrictive lung disease

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6
Q

methacholine challenge

A

for asthma

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7
Q

amiodarone lung

A

2-4 months at doses greater than 400mg/day

lipid laden foamy alveolar macrophages

organizing pneumonia - 25% of cases - mimics infectious pneumonia

ARDS - post-surgical

diffuse alveolar damage

solitary lung mass

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8
Q

50yo M increasing SOB with exercise, no fever, hemoptysis, weight loss, dry cough, no smoking, lungs crackle, clubbing, diffuse linear opacities, restrictive PFT, decreased diffusion capacity

A

most likely diagnosis

-idiopathic pulmonary fibrosis

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9
Q

27yo F SOB reently, exercise tolerance dwindled, occasional dry cough, no smoking, O2 90% after exercise, bilateral hilar lymph nodes, restrictive PFT

A

next appropriate step
-obtain transbronchial lymph node biopsy

diagnostic for sarcoidosis**

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10
Q

61yo F 3 day history of SOB, non-prod cough, fever, hemoptysis 3mL maroon, hx of SLE, cerebritis, lupus nephritis

T 100.4
CXR diffuse b/l infiltrates

A

PFT increased DLCO - most likely diagnosis

diffuse alveolar hemorrhage

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11
Q

causes of increased DLCO

A

diffuse alveolar hemorrhage

polycythemia

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12
Q

30yo M syncope, no fever, nonsustained V-tach, positive skin test for anergy, bilateral hilar adenopathy, elevated serum calcium, echo wall abnormality

bx of myocardium

A

upon receiving biopsy results you will

-begin tx for disorder associated with noncaseating granulomas

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13
Q

noncaseating granulomas

A

sarcoidosis

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14
Q

22yo F severe dyspnea on exertion, over last 6 months, O2 desat with exercise, enlarge pulmonary vasculature, V/Q normal, right heart strain, DLCO and PFT normal

A

next test to order for Dx?

right heart cath
-assess cause of pulmonary HTN

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15
Q

30yo M 15py tobacco, URI tx with azithromycin 3 weeks ago, 3 days ago SOB, cough hemoptysis, lips cyanotic, 2 + edema, BUN 60, Cr 4, microscopic hematuria

A

most help confirm dx

C-ANCA

wegners

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16
Q

C-ANCA

17
Q

anti-GM BM antibodies

18
Q

kveim test

19
Q

alpha1 antitrypsin

A

early emphysema

20
Q

goodpastures vs. wegners

A

history of URI - possible sinus involvement

21
Q

37yo AA M raised red lesions on anterior both legs, SOB, dry cough, no fever, never smoked, dry rales b/l, irregular heart rhythm, AV block, hilar adenopathy, noncaseating granulomas, PFT restrictive, elevated Ca and ACE

A

erythema nodosum

-sarcoidosis

Tx plan - high dose systemic corticosteroids

treat a patient that is symptomatic**

22
Q

hilar adenopathy without symptoms

A

sarcoidosis

-tx watchful waiting

23
Q

75yo M severe dyspnea 1 year, 100py tobacco, stone engraver, expiratory crackles b/l, clubbing, eggshell calcifications of hilar lymph nodes

A

most likely dx

-silicosis

24
Q

eggshell calcifications

25
asbestosis CXR
pleural plaques
26
TB CXR
hilar adenopathy upper lung fields
27
50yo F acute dyspnea, dry cough, SOB, malaise, fever, pH 7.3, diffuse alveolar infiltrates - suggest ARDS, CT b/l ground glass with little honeycombing, septal thickening and subpleural distribution of opacities lung bx - diffuse alveolar damage ventilation, steroids, antibiotics, death
acidosis - respiratory ground glass - alveolar filling - more treatable most likely dx -acute interstitial pneumonia
28
38yo M, albuterol, salmeterol, ipratropium, steroid inhaler, steroid taper for aspergillus elevated IgE, hack and cough, purulent blood tinged sputum, cough for years, 60yr tobacco, four teacups of sputum/day, dyspnea over years, crackles and rhonchi
CXR findings in this disease? mucus filled dilated bronchi with parallel linear opacities bronchiectasis allergic pulmonary aspergillosis - can lead to bronchiectasis
29
bronchiectasis with aspergillus
allergic pulmonary aspergillosis
30
49yo M CXR pre-op workup, small nodules left lung field laterally, high res CT, pleural based opacities, pleural plaques, restrictive PFT, decreased DLCO
most important to know -occupational history sounds like asbestosis brake lines, house work, insulation, mining, ship building
31
37yo M - 2-3 weeks dyspnea, hemoptysis, sinusitis, epistaxis UA RBC and WBC CXR - bilateral nodular infiltrates - one is cavitary
positive for C-ANCA likely wegners
32
tuberculosis
fever, chills, night sweats, malaise, weight loss, lymphadenopathy, cavitary lung lesions - upper lobes
33
goodpasture
renal and lung involvement
34
elevated ACE
sarcoidosis | -nonspecific
35
29yo M chronic cough and sputum production, 3 courses of antibiotics per year, recurrent chronic sinusitis and otitis media, grain storage facility, CT thick/dilated peripheral airways in lower lobes
evaluation should include - sweat chloride - CF - serum Ig levels - nasal mucosal Bx - with electron microscopy (for kartageners) - serum protein electrophoresis Dx - cystic fibrosis
36
27yo F cough, fever, night sweats, weight loss, marked eosinos, non-cavitating lung lesions, CXR nonsegmental alveolar infiltrates Tx with albuterol and oral corticosteroids - infiltrates resolve in 2 days - becomes asymptomatic returns 3 weeks with diarrhea and same symptoms
churg strauss syndrome vasculitis with initial asthma symptoms also get GI sx, possible heart disease