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?

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
lamellated calcified structures, usu in giant cells
schaumann bodies
26
star shaped eosinophilic bodies mad eup of compressed intermediate filaments
asteroid bodies
27
what is the prognosis for ppl with sarcoidosis?
65-75% recover (favorable prognosis)
28
occupational disease, moldy hay, involves primarily alveoli
hypersensitivity pneumonitis
29
inhalation of what sort of Ag induces hypersensitivity pneumonitis?
spores of thermophilic bacteria, true fungi, animal proteins, bacterial products
30
acute presentation of hypersensitivity pneumonia
severe dyspnea, cough, high fever, chills within 4-6 hrs, resolves spontaeously
31
chronic presentation of hypersensitivity pneumonia
prolonged exposure to small amts of Ag; insidious onset of dyspnea, cough, fatigue, respiratory failure
32
what type of hypersensitivity rxn is acute hypersensitivity pneumonitis?
type III
33
what type of hypersensitivity rxn is chronic hypersensitivity pneumonitis?
type IV
34
when hypersensitivity pneumonitis is caused by the spores of thermophilic actinomyces in hay?
farmers lung
35
silo filler's disease is due to?
NO2 gas
36
DIP (desquamative interstitial penumonia) is due to overabundance of___________?
smokers macrophages
37
what is desquamative interstitial penumonia? how to tx?
respiratory bronciolitis; tx with steroids
38
due to accumulation of acellular surfactant; cough up white jelly sputum; will see homogenous granular ppt within alveoli
pulmonary alveolar proteinosis (PAP)
39
how to tx PAP when it progresses?
whole lung lavage