lung pathology 3 Flashcards

1
Q

what is responsible for 1/6 of all deaths in US?

A

pneumonia

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2
Q

pyogenic bacteria w/ neutrophils in alveoli

A

acute pneumonia

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3
Q

not pyogenic, “atypical pneumonia” often viral or mycoplasmal

A

pneumonitis

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4
Q

what are some predisposing conditions for community acquired acute bacterial pneumonia?

A

age extremes, chronic diseases, immune deficiencies, decr splenic fxn

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5
Q

bacterial pneumonia often follows?

A

viral URI

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6
Q

which lobes are usually affected in bacterial pneumonia?

A

lower lobes or right middle lobe

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7
Q

what type of sputum will you get with bacterial pneumonia?

A

blood tinged sputum

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8
Q

most common cause of lobar pneumonia?

A

streptococcus pneumoniae (pneumococci)

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9
Q

congestion->red hepatization->gray hepatization->resolution assc’d wtih what type of pneumonia?

A

lobar pneumonia morphology

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10
Q

indications for hospitalization of CAP patient?

A
  1. severe dyspnea or hypoxemia
  2. empyema’
  3. CHF or COPD
  4. delirium
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11
Q

lack of alveolar exudate, modestly incr WBC, very little sputum, acute febrile respiratory disease with patchy inflammation in lung

A

primary atypical pneumonia; AKA interstitial pneumonitis

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12
Q

primary atypical pneumonia is largely confined to where?

A

alveolar septa & interstitium

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13
Q

what is the most common cause of primary atypical pneumonia (walking pneumonia)

A

mycoplasma

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14
Q

what is the 2nd most common cause of atypical pneumonia?

A

chlamydia pneumoniae

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15
Q

military, college students, schools, prisons, hospitals - what bug?

A

mycoplasma

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16
Q

coryza?

A

cold

17
Q

pathogenic mechanism of atypical pneumonia

A

organisms attach to respiratory epithelium–>cells necrose–>inflammatory response–>can extend to alveoli & interstitial inflammation

18
Q

thickening of the alveolar wall will be seen in what sort of pneumonia?

A

interstitial (atypical) pneumonia

19
Q

systemic disease that causes classic well formed non-caseating granulomas in many tissues and organs

A

sarcoidosis

20
Q

how to dx sarcoidosis?

A

dx of exclusion

21
Q

nonsmoker, af am female, SE US, young adults - what disease?

A

sarcoidosis

22
Q

if sarcoidosis has an acute onset, what is it?

A

fever, erythema nodosum, polyarthritis, incr IgG, incr Ca, incr ACE

23
Q

interstitial & intraalveolar accumulation of CD4, incr levels of IL2 & IFN gamma, IL8, TNF

A

sarcoidosis

24
Q

what type of bodies can be found in sarcoidosis bodies?

A
  1. schaumann bodies

2. asteroid bodies

25
Q

lamellated calcified structures, usu in giant cells

A

schaumann bodies

26
Q

star shaped eosinophilic bodies mad eup of compressed intermediate filaments

A

asteroid bodies

27
Q

what is the prognosis for ppl with sarcoidosis?

A

65-75% recover (favorable prognosis)

28
Q

occupational disease, moldy hay, involves primarily alveoli

A

hypersensitivity pneumonitis

29
Q

inhalation of what sort of Ag induces hypersensitivity pneumonitis?

A

spores of thermophilic bacteria, true fungi, animal proteins, bacterial products

30
Q

acute presentation of hypersensitivity pneumonia

A

severe dyspnea, cough, high fever, chills within 4-6 hrs, resolves spontaeously

31
Q

chronic presentation of hypersensitivity pneumonia

A

prolonged exposure to small amts of Ag; insidious onset of dyspnea, cough, fatigue, respiratory failure

32
Q

what type of hypersensitivity rxn is acute hypersensitivity pneumonitis?

A

type III

33
Q

what type of hypersensitivity rxn is chronic hypersensitivity pneumonitis?

A

type IV

34
Q

when hypersensitivity pneumonitis is caused by the spores of thermophilic actinomyces in hay?

A

farmers lung

35
Q

silo filler’s disease is due to?

A

NO2 gas

36
Q

DIP (desquamative interstitial penumonia) is due to overabundance of___________?

A

smokers macrophages

37
Q

what is desquamative interstitial penumonia? how to tx?

A

respiratory bronciolitis; tx with steroids

38
Q

due to accumulation of acellular surfactant; cough up white jelly sputum; will see homogenous granular ppt within alveoli

A

pulmonary alveolar proteinosis (PAP)

39
Q

how to tx PAP when it progresses?

A

whole lung lavage