Lec 15 ARDS Path Flashcards

1
Q

Histologically what do you see with acute lung injury / ARDS?

A

mostly = see diffuse alveolar damage

less common = diffuse alveolar hemorrhage, acute eosinophilic pneumonia

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2
Q

What is acute interstitial pneumonia?

A

idiopathic diffuse alveolar damage

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3
Q

What are some common causes of ARDS?

A
  • fulminant infection
  • post trauma
  • drug overdose
  • sepsis
  • aspirations
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4
Q

What is pathogenesis of diffuse alveolar damage?

A
  • not well understood

injury related to vascular endothelium and alveoli results in excess vascular fluid and protein leakage [early]

later –> cellular necrosis, epithelial hyperplasia, inflammation, fibrosis

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5
Q

What is pathology of DAD?

A
  • acute diffuse alveolar damage + necrosis of type I pneumoncytes
  • exudation of protein rich fluid into alveolai that organizes into hyaline membranes

recovery = hyperplasia of type II pneumocytes and interstitial fibrosis

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6
Q

What are the 3 overlapping phases of DAD?

A
  • exudative phase [days 1-7]
  • proliferative/organizing [7-12]
  • fibrotic phase [> 21 days]
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7
Q

What are gross features of lungs in ARDS?

A
  • wet
  • boggy
  • airless
  • heavy
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8
Q

What do you see in exudative phase of DAD [1st wk after injury]?

A
  • interstitial and alveolar edema
  • fibrin exudate
  • hyaline membranes [days 3-7]
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9
Q

What is simple eosinophilic pneumonia? What usually causes it?

A
  • mild self limited pulmonary infiltrates + peripheral blood eosinophilia

usually due to ascaris

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10
Q

What do you see in tropical eosinophilic pneumonia? What usually cause it?

A

high fever, wheezing, peripheral blood eosinophilia

usually 2ndary to filarial infection

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11
Q

What do you see in chronic eosinophilic pneumonia?

A

subacute illness; fever dyspnea peripheral blood eosinophilia

patchy infiltrates that resolve + reappear in same location

pt usually has asthma history

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12
Q

Who get chronic eosinophilic pneumonia? What causes it?

A
  • seen in patients with asthma history

can be idiopathic or due to drug toxicity, L-tryptophan ingestion, fungus, parasites

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13
Q

What do you see in acute eosinophilic pneumonia?

A
  • acute onset respiratory failure + severe hypoxemia

often have no peripheral blood eosinophilia; usually no history of asthma

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14
Q

What do you see clinically/histologically in eosinophilic pneumonia?

A
  • intra-alveolar fibrin, macrophages, abundant eosinophils, eosinophil microabscesses

+/- organizing pneumonia

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15
Q

Eosinophilic pneumonia is sensitive to what treatment?

A

sensitive to steroids

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16
Q

How do people with acute eosinophilic pneumonia represent?

A

may present with respiratory failure = clinically have ARDS

17
Q

What do you see histologically in acute eosinophilic pneumonia?

A

hyaline membranes like those in DAD but plus eosinophils

18
Q

What are histo features of classic/chronic EP?

A

intra-alveolar fibrin and macrophages

organizing pneumonia

19
Q

What is organizing pneumonia?

A

airspace organization = loos connective tissue in alveolar seen as common manifestation of lung injury as lung attempts repair

20
Q

What are some settings where you see organizing pneumonia?

A
  • as primary porcess [OP pattern]
  • as component of another process [HSP, acute pneumonia]
  • secondary reaction adjacent to unrelated process [next to tumor, granuloma, abscess]
21
Q

What is organizing pneumonia pattern?

A

specific pattern of organizing pneumonia centered around small airways

presents in subacute way with SOB and cough

22
Q

What do you see histologically in OP pattern of organizing pneumonia?

A
  • patchy bronchiolocentric organizing pneumonia
  • may have fibroblastic plugs in small airway lumens
  • minimal chronic inflammation in adjacent alveoli
  • interveneing lung is normal
  • no other significant findings
23
Q

What are potential etiologics of OP pattern?

A
  • associated wtih collagen vascular disease, drug reaction
24
Q

What do you call idiopathic OP pattern?

A

cryptogenic organizing pneumonia [COP]