Lung Pathology IV Flashcards

(44 cards)

1
Q

desquamative interstitial pneumonia

A

lots of smokers macrophages in alveoli

NOT desquamative

> 50yo
Male

Tx - steroids and cessation of smoking

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2
Q

respiratory bronchiolitis associated interstitial lung disease

A

pigmented macrophages in bronchioles
-peribronchiolar fibrosis

30+ pack year history

Tx - stop smoking

**not as bad as macros in alveoli

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3
Q

pulmonary langerhans cell histiocytosis

A

eosinophilic granuloma

proliferating dendritic cells
-response to smoking

Tx - stop smoking

express CD1a, S-100, CD207

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4
Q

CD1a

A

seen in pulmonary langerhans cell histiocytosis

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5
Q

pulmonary alveolar proteinosis

A

cough and gelatinous chunky sputum

bilateral, patchy CXR

accumulation of acellular surfactatnt in intra-alveolar and bronchiolar spaces

autoimmune
secondary
congenital - fatal

Tx - pulmonary lavage and GM-CSF therapy or transplant

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6
Q

accumulation of acellular surfactant in intraalveolar bronchiolar spaces

A

pulmonary alveolar proteinosis

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7
Q

ABC3 gene mutation

A

pulmonary alveolar proteinosis

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8
Q

pulmonary embolism

A

SOB, chest pain, swollen leg

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9
Q

saddle embolus

A

massive PE - death

  • massive stress on right heart
  • right side HF

PEA

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10
Q

fever, chest pain, SOB, electromechanical dissociation, sudden death

A

pulmonary embolism

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11
Q

mismatch of V/Q

A

pulmonary embolus

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12
Q

gold standard for PE

A

angiography

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13
Q

other emboli

A

fat - has vacuoles
amniotic fluid - blue lines
air - iatrogenic
nitrogen - divers

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14
Q

amniotic fluid emboli

A

during delivery

  • can lead to DIC
  • many patients die
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15
Q

Fen/Phen

A

interstitial fibrosis of lung

led to pulmonary HTN

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16
Q

bush tea

A

backyard tea

can lead to pulmonary HTN

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17
Q

primary pulmonary arterial HTN

A

80% genetic

idiopathic

mostly females 20-40yo

autosomal dominant

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18
Q

BMPR2 mutation

A

idiopathic primary pulmonary arterial HTN

BMPR2 - inhibits proliferation of vascular smooth m

19
Q

secondary pulmonary HTN

A

normal rxn of arteries to increased pressure

medial hypertrophy

narrows arteries
-further increase P

lead to cor pulmonale

20
Q

atheromas

A

form with pulmonary HTN

21
Q

plexiform

A

severe long standing pulmonary HTN leads to oblitered lumen and revascularization**

22
Q

diffuse alveolar hemorrhage syndrome

A

causes

  • goodpastures
  • idiopathic pulmonary hemosiderosis
  • vasculitis

hemosiderin laden macrophages

23
Q

alpha3 chain of collagen IV

A

anti-BM membrane antibodies

-goodpasture syndrome

24
Q

proliferative rapidly progressive GN and necrotizing hemorrhagic interstitial pneumonitis

25
goodpasture
M young smokers teens-20yo pulmonary and renal symptoms Tx - immunosuppression and plasmapharesis
26
SOB, proteinuria, hematuria, elevated Cr, couging up blood, hemoptysis
goodpasture
27
linear anti-BM deposits
lung and kidney goodpasture
28
idiopathic pulmonary hemosiderosis
rare, children diffuse hemorrhage hemosiderin deposition in macrophages and alveolar walls Tx immunosuppression bloody cough, weight loss, anemic
29
cANCA
PR3 wegeners
30
wegener granulomatosis
necrotizing granulomatous arteritis of lungs wegeners
31
upper resp lesions, vasculitis with granulomas, kidney problems
triad for wegeners
32
pulmonary infectious disease
often viral
33
splenectomy pts
lose ability to mount response to encapsulated pneumococcus**
34
COPD pneumonia
haem influenza | gram - pleomorphic
35
gram - pleomorphic
haem influenza COPD pneumonia
36
splenectomy/sickle cell pneumonia
streptococcus pneumonia | gram + diplococci
37
post viral pneumonia
staph aureus | gram + cocci
38
cystic fibrosis pneumonia
pseudomonas aeruginosa | gram - coccobacilli
39
gram + diplococci
streptococcus pneumonia | splenectomy/sickle cell
40
gram + cocci
staph aureus | post viral pneumonia
41
legionella
macrophage response - not neutrophils
42
debilitaed/malnourished pneumonia
klebsiella pneumoniae | gram - rod
43
cold agglutinins
mycoplasma pneumoniae
44
atypical pneumonias
chlamydia viruses mycoplasma coxiella