Airway Disease Pathology Flashcards

1
Q

what is the gross characteristic of lungs with bronchiectasis?

A

they will have really large airways grossly and on CT

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2
Q

the mucous inside of airways with bronchiectasis will have what cell type as a majority?

A

neutrophils

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3
Q

name three ways to have impairment of mucus flow

A

obstruction to outflow
abnormal mucus
abnormal ciliary function

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4
Q

explain how CF leads to mucous build up in the airways

A

the CFTR channel that leads to Cl transport is not functioning properly and the H20 in the airway comes out and follows the salt and then more mucous moves into the airway

normally the Cl is pumped into the airway and supports the mucous but in CF it is pumped out and the mucous is dehydrated

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5
Q

why does CF cause elevated sweat chloride?

A

because the Cl transporter is not functioning and the Cl gets trapped in the sweat duct

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6
Q

what is the problem with cilia in primary cilia dyskinesia?

A

the dynein arms are not present so motility is hindered

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7
Q

name the five histologic changes of note in asthma

A
thickened basement membrane
smooth muscle thickening
mucous cell hyperplasia
eosinophilia
thickened intralumenal mucus
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8
Q

what are charcot leyden crystals? what disease do we see these with?

A

these are crystals of the eosinophilic contents that can be seen on sputum

IN asthma

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9
Q

what are Curschmann spirals? what disease?

A

these are mucus casts of small airways that can be seen in asthma

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10
Q

what are two weird findings in sputum for asthma?

A

Curshmann spirals

charcot leyden crystal

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11
Q

what is the main histologic change seen in chronic bronchitis?

A

mucous cellular and glandular hyperplasia

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12
Q

upper lobe emphysema is suggestive of what etiology?

A

smoking

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13
Q

lower lobe emphysema is suggestive of what etiology?

A

a1 antitrypsin deficiency

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14
Q

will smoking lead to panlobular or centrilobular emphysema?

A

centrilobular

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15
Q

will a1 antitrypsin deficiency lead to panlobular or centrilobular emphysema?

A

panlobular

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16
Q

what age usually presents with A1AT deficiency?

A

under age 40

young adults

17
Q

what is the inheritance pattern of A1AT?

A

autosomal recessive

18
Q

where is A1AT made?

A

liver

19
Q

what is the gene that codes for A1AT?

A

SERPINE1

20
Q

what happens in the liver with A1AT deficiency?

A

the misfolded proteins can build up in the rER

21
Q

what is the name of the really bad mutation in A1AT?

A

PiZ