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66 Cards in this Set

  • Front
  • Back
95% of emphysema is ___, which is characteristic of ___.
centriacinar
smokers
centriacinar emphysema is in ___ lobes because ___
upper lobes
worse perfused -> less A1AT
panacinar emphysema is associated with ___. it occurs in ___ because ___.
A1AT deficiency
lower lobes
better perfused -> more inflammation
normal A1AT phenotype is ___. phenotype most common in A1AT deficiency is ___.
PiMM
PiZZ
all pts with PiZZ phenotype have ___, but only 10% get ___, due to ___.
A1AT accumulated in ER
liver disease
dysfunctional degradation/autophagocytosis
in neonates, A1AT deficiency presents with ___ (2). in adolescents it presents with ___ (2).
hepatitis
cholestatic jaundice
hepatitis
cirrhosis
PiZZ pts have 2-3% risk of ___
HCC
paraseptal emphysema occurs near ___ and at ___. in young adults it can cause ___
pleura
lobular margins
spontaneous pneumothorax
airspace enlargement with fibrosis is aka ___ (2). it presents with ___.
irregular emphysema
scar emphysema
nothing-asymptomatic
smoking causes neutrophils to release ___ (2).
ROS
neutrophil elastase
smoking causes release of ___ (3 cytokines)
LTB4
IL-8
TNF
tissue damage from ___ (2) causes macrophages to release ___ (2)
ROS
neutrophil elastase
MQ elastase
MMPs
clinical symptoms of emphysema begin when ___ of tissue has been damaged
1/3
smoking inactivates ___, e.g. ___
anti-elastase
A1AT
T/F: emphysema patients are poorly oxygenated
false: well oxygenated (pink)
4 histopath changes in chronic bronchitis
mucus gland enlargement
goblet cell hyperplasia
squamous metaplasia
narrowing of bronchioles
reid index is ___
ratio of thickness of mucous gland layer to thickness of wall from BM to cartilage
normal reid index is ___
0.4
T/F: chronic bronchitis pts are poorly oxygenated
true (blue)
6 kinds of mediators involved in asthma
AA metabolites
ACh
HA
PAF
cytokines
chemokines
4 AA metabolites in asthma
LTC4
LTD4
LTE4
PGD2
3 cytokines in asthma
IL-1
IL-6
TNF
asprin-sensitive asthma is associated with ___ (2)
rhinitis
nasal polyps
mucous plugs contain ___ (2)
Curchmann spirals
Charcot-Leyden crystals
Curschmann spirals are made of ___
shed epithelium
4 kinds of causes of bronchiectasis
postinfectious
immune-mediated
congenital
obstructive
postinfectious bronchiectasis is mainly after ___
necrotizing pneumonia
4 congenital conditions causing bronchiectasis
CF
Kartagener
intralobar sequestration
immunodeficiency
4 immune conditions causing bronchiectasis
GVHD
IBD
RA
SLE
bronchiectasis presents with ___ (4)
cough
fever
lots o sputum
hemoptysis
3 complications of bronchiectasis
cor pulmonale
brain abcess
amyloidosis
bronchiectasis involves one/both of upper/lower lobes, unless it's caused by ___
both
lower
obstruction
idiopathic pulmonary fibrosis is characterized by repeated cycles of ___
alveolitis
IPF is driven by ___ (molecule)
TGFb
IPF mainly affects ___ lobes
lower
microscopic presentation of IPF is called
usual interstitial pneumonia (UIP)
histopath of UIP has ___ heterogeneity and ___ (4)
temporal
type 2 pneumocyte hyperplasia
honeycomb fibrosis
fibroblastic foci
inflammation
fibrosis in IPF is highlighted with ___ stain
masson trichrome
CV complication of IPF
pulmonary HTN
age range for IPF is ___. for nonspecific interstitial pneumonia (NSIP) it's ___.
40-70
46-55
in contrast to IPF, NSIP has ___ fibrosis and no ___.
diffuse
temporal heterogeneity
BOOP is ___. it is aka ___.
bronchiolitis obliterans with organizing pneumonia
cryptogenic organizing pneumonia (COP)
BOOP is always ___.
idiopathic
___ in alveoli is characteristic of BOOP
fibrin
sarcoidosis is more common in men/women
sarcoidosis is more common in whites/blacks
women
blacks
sarcoidosis has a dx by ___, specifically ___.
exclusion
exclusion of TB
cytokines involved in granuloma formation
MIP-1alpha
IL-8
TNF
PPD rxn in sarcoidosis
anergy
sarcoidosis has ___ ___gammaglobulinemia
polyclonal
hyper
sarcoidosis is associated with HLA ___ (2)
A1
B8
sarcoidosis may be triggered by ___ (2)
mycobacteria
Rickettsia
7 extrapulmonary sites of sarcoidosis granulomas
spleen
liver
BM
skin
eye
salivary glands
muscle
2 characteristic histopath findings in sarcoidosis
asteroid bodies
Schaumann bodies
2 smoking-related interstitial diseases
desquamative interstitial pneumonia (DIP)
respiratory bronchiolitis-associated ILD (RB-ILD)
DIP usually presents at age ___ with ___ (2)
40
dyspnea
dry cough
DIP and RB-ILD has good/bad prognosis after ___ (2)
good
steroids
smoking cessation
DIP histopath finding
MQs in alveoli
DIP and RB-ILD both have ___ male/female ratio
2/1
___ prevents progression to fibrosis in hypersensitivity pneumonitis
removal of allergen
2 drugs associated with hypersensitivity pneumonitis
MTX
nitrofurantoin
2 drugs associated with bronchospasm
aspirin
beta-blockers
2 drugs associated with pneumonitis and fibrosis
bleomycin
amiodarone
T/F: ARDS responds to O2 therapy
false
2 phases of ARDS
acute
organizing
acute phase of ARDS is characterized by ___ (3)
congestion
inflammation
fibrin (hyaline membrane)
organizing phase of ARDS is characterized by ___ (2)
thickened alveolar septa
type 2 pneumocyte hyperplasia