Pulmonary Disorders Flashcards

(39 cards)

1
Q

Obliterative bronchiolitis

A
  • Caused by adenovirus

* Bronchiolitis —> healing by fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

RSV

A
  • Nosocomial infection of children
  • Usually self-limited
  • May cause disorganized epithelium and severe distention (? displaced surfactant)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Whooping cough

A
  • Bordetella pertussis

* May cause bronchiectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Candida albicans

A

•May produce mucosal ulceration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Bronchocentric granulomatosis

A
  • In asthmatic pts: allergic aspergillosis

* Non-asthmatic pts: TB or histoplasma; often coincides w/ autoimmune disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Right middle lobe syndrome

A

Collapse of R middle bronchus from hilar lymphadenopathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Strep pneumoniae

A
  • Young to middle-aged adults
  • Lobar PNA
  • S/p aspiration of pneumococci or viral URI
  • “Rusty” sputum, alveolar filling on CXR
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Klebsiella pneumoniae

A
  • Lobar PNA

* Mucoid lung surfaces, bulging lobes, tissue necrosis/abscesses —> bronchopleural fistula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Staph aureus

A
  • Common in CF pts, nosocomial infection

* Many small abscesses; may create pneumatoceles (cystic spaces)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Group B strep

A

Newborns; Sx look like respiratory distress syndrome; w/ severe toxemia, rapid death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Legionella

A
  • Hard to Cx
  • Contaminated water
  • Widespread bronchopneumonia w/ necrosis of inflammatory cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Pseudomonas aeruginosa

A
  • Immunocompromised, burns, CF

* Occurs w/ vasculitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Mycobacterium

A
  • Ghon lesion: granuloma at periphery of lung
  • Miliary TB: multiple small granulomas in many organs
  • M. avium-intracellulare: immunocompromised, extensive macrophage infiltrate w/ innumerable acid-fast orgs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Actinomycosis

A
  • Multiple small lung abscesses
  • Gram + filamentous bacteria
  • Sulfur granules
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Nocardia

A
  • Beaded, thin filaments w/ R angle branching

* Pts w/ lymphomas, neutropenia, chronic granulomatous disease, alveolar proteinosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Histoplasmosis

A
  • Midwest & South
  • Inhalation of bird droppings
  • Resembles TB
  • Granulomas prone to calcification
17
Q

Aspergillosis

A
  • AIDS pts or pts on cytotoxic therapy
  • Invasive: blood vessel invasion —> thrombosis, lung infarcts
  • Aspergilloma: fungus ball grows in pre-existing cavity
  • Allergic bronchopulmonary aspergillosis: eosonophilia, increased serum IgE, proximal bronchiectasis
18
Q

Pneumocystitis jiroveci

A
  • Fungus
  • Interstitial infiltrates, type 2 pneumocyte hyperplasia
  • Alveoli filled w/ foamy exudate
19
Q

CMV

A
  • Interstitial infiltration

* Cytomegaly w/ nuclear inclusion

20
Q

Diffuse alveolar damage

A
  • Causes ARDS
  • Triggered by variety of insults
  • Hyaline membranes and collagen deposition in alveolar walls
  • Leakage of plasma proteins
  • “Honeycomb lung”
21
Q

Goodpasture syndrome

A

Diffuse alveolar hemorrhage, glomerulonephritis, Ab to basement membrane

22
Q

Eosinophilic PNA

A
  • Loeffler syndrome: Mild or asymptomatic PNA with eosinophilia
  • Acute/chronic: allergy association
  • Infectious: parasites
23
Q

Lipid PNA

A
  • Endogenous: secondary to bronchial obstruction

* Exogenous: aspirated oils

24
Q

Alpha 1-antitrypsin deficiency

A
  • A1AT is an inhibitor of proteinases including elastases
  • Lack of inhibition leads to alveolar wall destruction
  • Possible liver disease
25
Silicosis
*  Simple nodular: progression of 10-40 yrs; "whorled" collagen nodules containing needle-shaped silicates; possible "eggshell calcification" of nodes *  Progressive massive: nodules 2-10 cm wide w/ central cavitation *  Acute: progression of a few yrs; no nodules; alveoli contain eosinophilic material
26
Coal workers' pneumoconiosis
*  Anthracosis or anthracosilicosis *  Scattered 1-4 mm black foci *  Carbon-laden macrophages
27
Asbestos
*  Diffuse interstitial fibrosis *  Asbestos bodies: long, thin fiber surrounded by iron-protein coat *  Plaque on parietal pleura *  Mesothelioma
28
Berylliosis
*  Aerospace, industrial ceramics, or nuclear industries | *  Noncaseating granulomas
29
Talcosis
*  Variable pathology *  FB granulomas w/ plate-like particles *  Associated w/ IV drug use
30
Acute hypersensitivity pneumonitis
*  Acute or chronic interstitial inflammation | *  Chronic may have poorly formed granulomas, organizing PNA
31
Sarcoidosis
*  Can also involve nodes, skin, eye *  More common in African-Americans *  CD4 helper cells form multiple noncaseating granulomas *  Along pleura, interlobular septa, around bronchovascular bundles, bronchial submucosa (diagnose via bronchoscopic biopsy) *  Can progress to onion-skin fibrosis around giant cells
32
Idiopathic pulmonary fibrosis
*  Patchy interstitial fibrosis adjacent to normal lung *  Loose fibroblastic tissue adjacent to dense collagen *  Epithelium grows into dilated airspaces *  Gradual DOE and dry cough over 1-3 yrs
33
Desquamative interstitial PNA
*  Smokers *  Alveolar architecture is preserved w/ minimal fibrosis *  Intra-alveolar macrophages contain golden-brown pigment
34
Respiratory bronchiolitis
*  Smokers | *  Pigmented macrophages centered on bronchioles
35
Langerhans cell histiocytosis
*  Smokers 20-40 *  Nodular infiltrates w/ stellate border *  Langerhans cells: eosinophilic cytoplasm, grooved nuclei *  Eosinophils
36
Lymphangioleiomyomatosis
*  Women of childbearing age *  Abnormal proliferation of smooth muscle in lung (? hormonal control) *  Tuberous sclerosis gene complex mutation
37
Pulmonary HTN
*  L to R shunt *  Recurrent PEs *  Hypoxemia *  LV failure
38
Pulmonary hamartoma
*  Usu. at periphery *  Popcorn calcification *  Several types of tissue interspersed w/ respiratory epithelium-lined clefts
39
Small cell carcinoma
•