Lung Pathology I Flashcards

(38 cards)

1
Q

aspiration

A

down right lung - straight bronchus

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2
Q

lying down

A

aspiration to left upper lobe

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3
Q

conducting vs. respiratory

A

respiratory - where alveoli gas exchange occurs

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4
Q

size of particles

A

less than 10 microns - alveolar damage

less than 5 microns - real bad damage to alveoli

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5
Q

bronchus

A

cartilage

AND submucosal glands

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6
Q

bronchiole

A

no cartilage

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7
Q

clara cells

A

in bronchioles

dome shaped cells with short microvilli

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8
Q

surfactant

A

type II pneumocytes

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9
Q

pores of kohn

A

intraalveolar macrophages

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10
Q

lobule

A

cluster of terminal bronchioles and all attached acini

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11
Q

acinus

A

resp bronchiole and all attached alveolar ducts and alveolar sacs

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12
Q

canals of lambert

A

openings between bronchi and alveoli

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13
Q

pulmonary hypoplasia

A

lungs don’t develop fully

-oligohydramnios - uterus squeeze fetus

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14
Q

TE fistula

A

most common - blind pouch

bloated belly - trachea connect to esophagus

blind pouch - can cause oligohydramnios during pregnancy

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15
Q

respiratory epithelium midline cyst in mediastinum or hilar location

A

bronchogenic congenital foregut cyst

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16
Q

squamous mucosa midline cyst

A

esophageal congenital foregut cyst

17
Q

intestinal mucosa midline cyst

A

enteric congenital foregut cyst

18
Q

congenital cystic adenomatoid malformation

A

hamartoma lesion with abnormal bronchiolar tissue

adenomatoid - confined to bronchioles

resp difficulty or recurring infection

type I - large good prognosis
type II - smaller , bad, other congen anomalies

19
Q

bronchopulmonary sequestrations

A

area of lung not connected to airways

blood supply - systemic arteries

20
Q

extralobar bronchopulmonary sequestrations

A

no connection to pulmonary circulation or bronchiole tree

21
Q

intralobar bronchopulmonary sequestrations

A

acquired - recurrent infection

-scarring of bronchi - stenotic

22
Q

true nuchal cord

A

neck wrapped with umbilical cord

-see compression strangulation marks

23
Q

hyaline membrane disease

A

neonatal respiratory distress syndrome

deficient surfactant - immature lungs

need to stress baby - more surfactant

  • stess = delivery
  • also - high insulin inhibits secretion
24
Q

glandular

25
saccular
30 weeks - not good air exchange - no surfactant
26
alveolar
term | -but at birth, lung still not mature
27
measure of surfactant
L/S ration > 2 mature <1 immature gold standard
28
foam stability index
shake to see suds
29
mechanism of hyaline membrane disease
``` no surfactant > atelectasis > hypoxemia > acidosis > endo and epi damage > plasma leak > fibrin and necrotic cells deposited = hyaline ``` occurs after birth**
30
preterm baby, mom DM, C section, low APGAR, become cyanotic, rales, reticulonodular ground glass
respiratory distress syndrome | -O2 therapy needed
31
RDS clinical
artifical surfactant steroids O2 therapy - risks of retinopathy and bronchopulmonary dysplasia
32
bronchopulmonary dysplasia
criteria - 28 days O2 therapy and 36 weeks post menstrual age alveolar hypoplasia and thick walls high O2 - decreases lung maturity arrest at SACCULAR stage
33
mucoviscidosis
cystic fibrosis disorder of epithelial transport mutation in CFTR genes
34
Dx of cystic fibrosis
history in sibling positive newborn screening result and - increased sweat chloride two or more occasions** - two CFTR mutations - abnormal epithelial nasal ion transport
35
delta508
mutations in CF
36
Tx of CF
``` pancreatic insufficiency vit deficiency pulmonary disease antibiotics hypertonic saline high dose ibuprofen ``` heart/lung transplant -cor pulmonale
37
antibiotics in CF
cover pseudomonas aeruginosa
38
ALTE
apparent life threatening event infants who have one are increased risk of future resp failure