Lung Pathology Flashcards

1
Q

What is bronchietasis and how would you diagnos it

A

Reccurent bronchial infection causing permenant dilation of bronchioles. See dilated bronchi on CT

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2
Q

What is the congenital form of COPD?

A

Alpha-1 antitrypsin def. –> pancincar emphysema and liver disease

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3
Q

Describe the cause of COPD

A

smoking –> abnormal inflammatory response –> ROS, CD8+, macrophages(protease) –> alveolar damage

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4
Q

Describe some causes of pulmonary fibrosis and how it is diagnosed.

A

Chest wall or lung disease ,loss of elasticity, decreased lung capacity, obesity, neuromuscular ds.
Dx: PFT, DLCO

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5
Q

What are some symptoms of ILD?

A

progressive DOE, non-productive cough, hypoxemia, pulmonary HTN, cyanosis, cor pulmonale

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6
Q

How do you distinguish non-specific interstitial pneumonitis from Idiopathic Pulmonary Fibrosis?

A

Non- specfic has fever in addition to dyspnea, hypoxemia, etc. Also see Subpleural fibrosis instead of diffuse interstitital. Also reticulonodular and honeycomb in IPF

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7
Q

In which ILD would you see migratory pulmonary infiltrates on CXR?

A

Cryptogenic organizing pneumonia

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8
Q

Which ILD’s respond to corticosteroids?

A

non-specific interstitial pneumonitis, crytpogenic organizing pneumonia, occupation/enviroment (not silica, asbestos, coal)

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9
Q

What are the CXR findings of silacosis?

A

small fibrotic nodules –> massive fibrosis
cavitaroy necrosis
hylar adenopathy w/ calcification

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10
Q

What are histological signs of asbestos

A

Asbestos bodies in lower lobe, calcified plural plaques

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11
Q

What is antracosis

A

blackening of the lung associated with pneumoconius (cola miner’s lung)
10% of times –> massive fibrosis

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12
Q

Which ILD is assiacated with smoking>

A

Pulmonary Langerhan cell histiocytes

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13
Q

A patient is suspected of having ILD and gets a pneumothorax What restrtictive disease do they likely have?

A

Pulmonary Langerhan Cell Histiocytosis

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14
Q

What population group is assocaited with sarcoidosis?

A

10-40 african american females

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15
Q

What CXR findings would you see on CXR of a sarcoidosis patient?

A

hilar adenopathy
reticularnodular opacity
non-casseating granulomas
CD4/CD8 > 3.5

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16
Q

Describe the 3 causes for pulmonary alveolar protenosis

A
  1. autoantibody to GM-CSF
  2. Secondary to dust exposure, allogenic marrow transplant, infection, heme malignancy
  3. mutation in gene for GM-CSF – fatal
17
Q

How woudl you diagnose pulmonary HTN?

A

loud P2

RVH on EKG

18
Q

Name some causes for pulmonary HTN.

A

Chronic, hypoxic vasoconstriction
mitral stenosis
primary from sclerderma/CT ds.
pulomnary vaso-occlusive ds

19
Q

An abrupt rapidly progressive cough, dyspnea and hemotoysis that has a 50% mortality could be this

A

diffuse alveolar hemorrhage syndrome