Ch 9 Pathoma Respiratory Tract Pathology (9.3-End) Flashcards

1
Q

Pneumonia is a ___ of the ___. It occurs when normal defenses are impaired. Name 3 normal defenses

A

infection; lung parenchyma; 1) cough reflex; 2) mucociliary escalator; 3) mucus plugging

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2
Q

Name 6 clinical features of pneumonia

A

1) fever and chills; 2) productive cough with yellow-green (pus) or rusty (bloody) sputum; 3) tachypnea w/pleuritic chest pain (bradykinin and PGE2); 4) decreased breath sounds; 5) dullness to percussion; 6) elevated WBC

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3
Q

Diagnosis of pneumonia is made in these 3 ways

A

1) chest xray; 2) sputum gram stain and culture; 3) blood cultures

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4
Q

Name the 3 patterns of pneumonia classically seen on chest X-ray (and what typically causes them)

A

1) lobar pneumonia; 2) bronchopneumonia; 3) interstitial pneumonia; (1 and 2 are usually bacterial, and 3 is usually viral)

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5
Q

Lobar pneumonia is characterized by ___ of a ___. Usually bacterial/viral/fungal. Most common causes are ___ (95%) and ___.

A

consolidation; entire lobe of the lung; bacterial; strep pneumo; Klebsiella pneumoniae

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6
Q

Name the 4 classic gross phases of lobar pneumonia (and what causes that)

A

1) congestion (due to congested vessels and edema); 2) red hepatization (due to exudate, neutrophils, and hemorrhage filling the alveolar air spaces, giving normally spongy lung a solid consistency; 3) gray hepatization (due to degradation of red cells in exudate); 4) resolution

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7
Q

Bronchopneumonia is characterized by ___ centered around ___. Often focal/multifocal and unilateral/bilateral. Caused by a variety of bacterial/viral/fungal organisms

A

scattered patchy consolidation; bronchioles; multifocal; bilateral; bacterial

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8
Q

Interstitial (___) pneumonia is characterized by ___. Presents with mild/moderate/severe ___ symptoms (minimal ___ and low __). “___” presentation. Caused by bacteria/virus/fungal infxn.

A

atypical; diffuse interstitial infiltrates (inflammation in wall of alveolar air sacs without consolidation); mild; upper respiratory; sputum; fever; atypical; bacteria and virus

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9
Q

Aspiration pneumonia is seen in pts at risk for ___ (e.g. __ and __ pts). Most often due to ___ in the ___. Name 3 common organisms. Classically resents in a right/left upper/lower lobe __.

A

aspiration; alcoholics; comatose; anaerobic bacteria; oropharynx; 1) Bacteroides; 2) fusobacterium; 3) peptococcus; right lower; abscess (anatomically the right main stem bronchus branches at a less acute angle than the left)

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10
Q

What is the most common cause of community-acquired pneumonia? In what patient age group is it seen in? What kind of pneumonia does it form?

A

Streptococcus pneumoniae (95%); middle-aged adults and elderly; lobar pneumonia

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11
Q

What is the most common cause of secondary pneumonia? What is the 2nd most common cause of secondary pneumonia? What kind of pneumonia do they cause?

A

Strep pneumo (lobar); staph aureus (bronchopneumonia)

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12
Q

Klebsiella pneumoniae is __ flora that is ___. It affects __ and ___ individuals, especially these 3 groups. It has a ___, which results in a ___ sputum (___). Often complicated by ___. It forms __ pneumonia

A

enteric; aspirated; malnourished; debilitated; elderly in nursing homes; alcoholics; diabetics; thick mucoid capsule; gelatinous; currant jelly; abscess; lobar

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13
Q

Staph aureus forms ___ pneumonia. It is the 2nd most common cause of ___. Often complicated by __ or ___.

A

bronchopneumonia; secondary pneumonia; abscess; empyema (pus in pleural space)

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14
Q

Name 5 organisms that cause bronchopneumonia

A

1) staph aureus; 2) haemophilus influenzae; 3) pseudomonas aeruginosa; 4) moraxella catarrhalis; 5) legionella pneumophila

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15
Q

Haemophilus influenzae forms __ pneumonia. It is a common cause of ___ and ___.

A

bronchopneumonia; secondary pneumonia; pneumonia superimposed on COPD (leads to exacerbation of COPD)

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16
Q

Pseudomonas aeruginosa forms __ pneumonia. It is seen in ___ patients.

A

bronchopneumonia; cystic fibrosis

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17
Q

Moraxella catarrhalis forms __ pneumonia. It is a common cause of ___ pneumonia and ___.

A

bronchopneumonia; community-acquired; pneumonia superimposed on COPD (leads to COPD exacerbation)

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18
Q

Legionella pneumophila forms ___ pneumonia. It is a common cause of ___ pneumonia, pneumonia ___, or pneumonia in ___. It is transmitted from ___. It is an extracellular/intracellular organism best visualized by ___.

A

bronchopneumonia; community acquired; superimposed on COPD; immunocompromised states; water source; intracellular; silver stain

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19
Q

What is the most common cause of walking pneumonia? Who does it usually affect?

A

Mycoplasma pneumoniae; young adults

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20
Q

Complications of mycoplasma pneumoniae atypical pneumoniae includes __ and __. How does it gram stain?

A

autoimmune hemolytic anemia (IgM against i antigen on RBCs causes cold hemolytic anemia); erythema multiforme; Not visible on gram stain due to lack of cell wall

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21
Q

What is the second most cause of atypical pneumonia in young adults? What is the most common cause of atypical pneumonia in infants? What causes atypical pneumonia in post transplant immunosuppressive therapy?

A

chlamydia pneumoniae; respiratory syncytial virus (RSV); CMV

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22
Q

Influenza virus causes ___ pneumonia in the __, __, and those with ___. It also increases risk for ____.

A

atypical pneumonia; elderly; immunocompromised; preexisting lung disease; superimposed S aureus or H influenzae bacterial pneumonia (thats what will kill you)

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23
Q

___ causes atypical pneumonia with high fever (__ fever). Seen in __ and ___.

A

Coxiella burnetti; Q; farmers, veterinarians

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24
Q

Coxiella is a ___ organism but it is distinct from most of those because of thee 3 reasons.

A

rickettsial; 1) causes pneumonia; 2) does not require arthropod vector transmission (survives as highly heat-resistant endospores); 3) does not produce a skin rash

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25
Q

Name 6 causes of interstitial (atypical) pneumonia

A

1) mycoplasma pneumoniae; 2) chlamydia pneumoniae; 3) respiratory syncytial virus; 4) CMV; 5) influenza virus; 6) coxiella burnetti

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26
Q

Tuberculosis is due to ____ of aerosolized ___. ___ TB arises with initial exposure.

A

inhalation; mycobacterium tuberculosis; primary

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27
Q

Primary TB results in __, ___ in the upper/lower lobe of the __ and __ that undergoes __ and __, forming a __ complex. Primary TB is generally symptomatic/asymptomatic, and causes a positive/negative PPD

A

focal, caseating necrosis; lower; lung; hilar lymph nodes; fibrosis; calcification; Ghon; asymptomatic; positive

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28
Q

Secondary TB arises with ___ of ___. Reactivation is commonly due to __, but may also be seen with __. Reactivation occurs at apex/base of lung. Forms cavitary foci of ___. May also lead to ___ or ___.

A

reactivation; Mycobacterium tuberculosis; AIDS; aging; apex (relatively poor lymphatic drainage and high oxygen tension); caseous necrosis; miliary pulmonary TB; tuberculous bronchopneumonia.

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29
Q

Clinical features of secondary TB include these 4

A

1) fever; 2) night sweats; 3) cough with hemoptysis; 4) weight loss

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30
Q

Biopsy of secondary TB reveals ___. When you see that on the differential is TB and ___. ___ stain reveals ___.

A

caseating granulomas; fungi; AFB; acid fast bacilli

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31
Q

Systemic spread of secondary TB often occurs and can involve ___. Common sites include these 4.

A

any tissue; 1) meningies (meningitis - often at base of brain); 2) cervical lymph nodes; 3) kidneys (most common; causes sterile pyuria); 4) lumbar vertebrae (Pott disease)

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32
Q

Chronic obstructive pulmonary disease is a group of diseases characterized by ____. The lung does not ___, and __ is trapped.

A

airway obstruction; empty; air

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33
Q

In COPD the volume of air that can be forcefully expired (__) is increased/decreased, especially during the first second of expiration (___). The ___ ratio is increased/decreased. Total lung capacity (TLC) is usually increased/decreased due to ___.

A

FVC; decreased; FEV1; FEV1:FVC; decreased (FEV1 is decreased more than the FVC is decreased!); increased; air trapping

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34
Q

Chronic bronchitis is a chronic ___ lasting at least __ over minimum of ___. Highly associated with ___. Characterized by ___ of ___, which leads to increased thickness of ___ relative to ___ (__ index increases to greater than __%; normal is less than __%).

A

productive cough; 3 months; 2 years; smoking; hypertrophy; bronchial mucinous glands; mucus glands; bronchial wall thickness; Reid; 50; 40

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35
Q

Name 3 clinical features of chronic bronchitis

A

1) productive cough due to excessive mucus production; 2) cyanosis (‘blue bloaters’), mucus plug trap CO2, leading to inc PaCO2 and dec PaO2; 3) increased risk of infxn and cor pulmonale (hypoxemic vasoconstriction leads to inc pHTN - RV hypertrophy - R sided HF)

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36
Q

Emphysema is the destruction of ___. There is a loss of ___ and there is ___ of airways during inhalation/exhalation, which results in __ and __.

A

alveolar air sacs; elastic recoil; collapse; exhalation; obstruction; air trapping

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37
Q

Emphysema is due to an imbalance of __ and __. Inflammation in the lung normally leads to release of ___ by ___ and ___. ____ neutralizes ___ (what is released).

A

proteases; anti-proteases; proteases; neutrophils; macrophages; alpha1-antitrypsin (A1AT); proteases.

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38
Q

What are the two pathways that result in emphysema and who gets which kind?

A

1) Excessive inflammation (smokers) 2) lack of A1AT (A1AT deficiency pts)

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39
Q

In emphysema, pollutants in smoke lead to excessive ___ and ___-mediated damage. It results in ___ emphysema that is most severe in the ___.

A

inflammation; protease; centriacinar; upper lobes

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40
Q

A1AT deficiency is a common/rare cause of emphysema. The lack of __ leaves the __ vulnerable to __-mediated damage. It results in __ emphysema that is most severe in the ___. ___ may also be present

A

rare; antiprotease; air sacs; protease; panacinar; lower lobes; liver cirrhosis

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41
Q

A1AT deficiency is due to ___ of the mutated protein. Mutant A1AT accumulates in the ___ of ___, resulting in ___. Biopsy reveals ___, ___-positive globules in ___.

A

misfolding; endoplasmic reticulum; hepatocytes; liver damage; pink; PAS; hepatocytes

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42
Q

___ is the normal allele for A1AT. Usually two copies are expressed (___). ___ is the most common clinically relevant mutation, which results in significantly low levels of circulating ___. ___ heterozygotes are usually ___, with decreased levels of __, but at risk for emphysema with __. __ homozygotes are at significant risk for ___ and ___.

A

PiM; PiMM; PiZ; A1AT; PiMZ; asymptomatic; smoking; PiZZ; panacinar emphysema; cirrhosis

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43
Q

Name 5 clinical features of emphysema

A

1) dyspnea and cough with minimal sputum; 2) prolonged expiration with pursed lips (pink-puffer); 3) weight loss; 4) increased anterior-posterior diameter of chest (‘barrel chest’); 5) hypoxemia (due to destruction of capillaries in alveolar sac) and cor pulmonale are late complications

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44
Q

Asthma is reversible/irreversible airway ___, most often due to ___ (___ asthma). Presents in ___, and is often associated with these 3 things.

A

reversible; bronchoconstriction; allergic stimuli; atopic; childhood; 1) allergic rhinitis; 2) eczema; 3) family hx of atopy

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45
Q

In asthma (type__ hypersensitivity), allergens induce __ phenotype in CD_+ T cells of genetically susceptible individuals. __ cells secrete these 3 cytokines

A

I; Th2; 4; Th2; IL-4, IL-5, IL-10

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46
Q

What does IL-4, 5, and 10 do?

A

IL-4: mediates class switch to IgE IL-5: attracts eosinophils IL-10: stimulates Th2 cells and inhibits

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47
Q

In asthma, reexposure to allergen leads to __-mediated activation of __ cells. In the early phase reaction, there is release of preformed ___ granules and generation of these 3 leukotrienes, which lead to __, __ and ___

A

Ig-E; mast; histamine; C4, D4, E4; bronchoconstriction; inflammation; edema

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48
Q

In asthma, the late phase reaction involves __, especially ___ derived from __, damages cells and perpetuates ___

A

inflammation; major basic protein; eosinophils; bronchoconstriction

49
Q

Name 3 clinical features of asthma (episodic)

A

1) dyspnea and wheezing; 2) productive cough; 3) severe, unrelenting attack can result in status asthmaticus and death

50
Q

In asthma, the productive cough classically has __-shaped __ (aka ___) and ___-derived crystals (___).

A

spiral; mucus plugs; Curschmann spirals; eosinophil; Charcot-Leyden crystals, which are aggregates of major basic protein

51
Q

Asthma may also arise from nonallergic causes. Name 4

A

1) exercise; 2) viral infxn; 3) aspirin (aspirin intolerant asthma - nasal polyps and bronchospasm); 4) occupational exposures

52
Q

Leukotrienes C4, E4, and D4 causes these 3 things

A

1) vasoconstriction; 2) increase vascular permeability; 3) bronchoconstriction

53
Q

Histamine induces ___ at ___ and increases ___ at __-

A

vasodilation; arterioles inc vascular permeability at post capillary venues

54
Q

Bronchiectasis is permanent ___ of ___ and ___. It is a loss of ___, which results in ___.

A

dilatation; bronchioles; bronchi; airway tone; air trapping

55
Q

Bronchiectasis is due to ___ with damage to ___. Name 5 causes.

A

necrotizing inflammation; 1) cystic fibrosis (thick secretions cause mucus plugging cause inc risk of infxn); 2) Kartagener syndrome (ciliary mvmt impaired causes inc risk of infxn); 3) Tumor/foreign body (block airway, inc risk of infxn); 4) Necrotizing infxn; 5) allergic bronchopulmonary aspergillosis

56
Q

Kartagener syndrome is a sporadic/inherited defect of the ___, which is necessary for ___. It is associated with these 3 things.

A

inherited; dynein arm; ciliary mvmt; 1) sinusitis; 2) infertility (poor motility of sperm); 3) situs inversus (position of major organs is reversed) pts with this can get bronchiectasis

57
Q

Allergic bronchopulmonary aspergillosis is a __ rxn to __, which leads to chronic inflammatory damage. Usually seen in individuals with __ or __.

A

hypersensitivity; aspergillus; asthma; cystic fibrosis *it is a cause of bronchiectasis

58
Q

Name 3 clinical features of bronchiectasis. Name 2 complications.

A

cough, dyspnea, foul-smelling sputum; 1) hypoxemia with cor pulmonale; 2) secondary amyloidosis

59
Q

In secondary amyloidosis, ___ leads to the production of an ___ (SAA), which is converted to ___, which is then deposited in tissues causing secondary amyloidosis.

A

chronic inflammation; acute phase reactant; AA

60
Q

Restrictive lung diseases are characterized by ____. What do you see with the TLC, FEV1, FVC, and FEV1:FVC ratio?

A

restricted filling of the lung; decreased TLC; decreased FEV1; very decreased FVC; increased FEV1:FVC ratio

61
Q

Restrictive lung disease is most commonly due to ___. May also arise with ___ (seen in pts with ___)

A

interstitial disease of the lung; chest wall abnormalities; massive obesity (force on chest wall makes it harder to expand, which makes it harder to open and fill the lungs)

62
Q

Idiopathic pulmonary fibrosis is fibrosis of ___. Etiology is ___. Likely related to ___. __ from injured pneumocytes induces fibrosis. Secondary causes of said fibrosis such as __ (name 2 examples) and ___ must be excluded.

A

lung interstitium; unknown; cyclical lung injury; TGF-B; drugs (bleomycin and amiodarone = anti-arryhthmic); radiation therapy

63
Q

Clinical features of idiopathic pulmonary fibrosis include progressive __ and __. __ is seen on lung CT. It is initially seen in ___ patches, but eventually results in diffuse ___ with end-stage ‘___’ lung. Tx is ___.

A

dyspnea; cough; fibrosis; subpleural; fibrosis; honeycomb; lung transplantation

64
Q

Pneumoconioses is ___ due to ___. It requires exposure to large/small particles that are ___. ____ engulf foreign particles and induce ___.

A

interstitial fibrosis; occupational exposure; small (large are easily filtered out); fibrogenic; alveolar macrophages; fibrosis

65
Q

Name 4 types of pneumoconiosis.

A

1) coal worker’s; 2) silicosis; 3) berylliosis; 4) asbestosis

66
Q

In coal worker’s pneumoconiosis, the exposure is __. Massive exposure leads to diffuse __ (‘___’). It is associated with ___ (___ syndrome).

A

carbon dust; fibrosis; black lung; rheumatoid arthritis; Caplan

67
Q

Mild exposure to carbon (from pollution) results in ___ (collection of carbon-laden ___). It is/is not clinically significant

A

anthracosis; macrophages; is not

68
Q

Silicosis is from exposure to ___, seen in ___ and ___. It causes __ nodules in ___ lobes of lung. It impairs ___ formation by macrophages. And you have an increased risk for ___.

A

silica; sandblasters; silica miners; fibrotic; upper; phagolysosome; TB

69
Q

Berylliosis is caused by exposure to ___. Seen in __ and ___. It causes ___ in the lung, hilar lymph nodes, and systemic organs (looks a lot like ___). There is an increased/decreased risk for lung cancer

A

beryllium; beryllium miners; workers in aerospace industry; noncaseating granulomas; sarcoidosis; increased

70
Q

Asbestosis is caused by ___ fibers. Seen in these 3 groups. It causes ___ and ___ of both the lung and pleura (which one is more common). Lesions may contain ___ (long, golden brown fibers with associated __).

A

asbestos; plumbers; construction workers; shipyard workers; fibrosis (plaques); increased risk for lung carcinoma and mesothelioma (lung cancer is more common); asbestos bodies; iron

71
Q

Sarcoidosis is a systemic/local disease characterized by ___ in multiple organs, most commonly these 2. It is classically seen in ___. Etiology is ___. Likely due to ___ response to an unknown antigen. Sarcoidosis leads to obstructive/restrictive lung disease.

A

systemic; noncaseating granulomas (means there is no necrosis in it); hilar lymph nodes; lung; African American females; unknown; CD4+ helper T cell; restrictive

72
Q

On histology, sarcoidosis causes characteristic ___ (‘___’), often seen within giant cells of the granulomas

A

stellate inclusions; asteroid bodies

73
Q

Besides from the lung and hilar lymph nodes, sarcoidosis commonly affects these 4 tissues.

A

1) uvea (uveitis); 2) skin (cutaneous nodules or erythema nodosum); 3) salivary; and 4) lacrimal glands (3 and 4 mimic Sjogren syndrome) Almost any tissue can be involved

74
Q

Name 3 clinical features of sarcoidosis (and which is most common), and treatment.

A

1) dyspnea or cough (most common); 2) elevated serum ACE; 3) hypercalcemia (1-alpha hydroxylase activity of epithelioid histiocytes converts vit D to its active form); tx is steroids, though it often resolves spontaneously w/o tx

75
Q

Hypersensitivity pneumonitis is a ___ reaction to inhaled ____ (eg ___). Presents with ___, ___, and ___ minutes/hours/days/weeks after exposure. Resolves with ___. Chronic exposure leads to ___.

A

granulomatous; organic antigens; pigeon breeder’s lung; fever, cough, dyspnea; hours; removal of the exposure; interstitial fibrosis

76
Q

Pulmonary hypertension is high pressure in the ___ circuit. Mean arterial pressure greater than __ mmHg; normal is __ mmHg. Can be sub classified as __ or __ based on etiology.

A

pulmonary; 25; 10; primary; secondary

77
Q

Pulmonary HTN is characterized by ___ of the pulmonary trunk, ___ hypertrophy of __ arteries, and ___. ___ are seen with severe, long standing disease. pHTN can lead to ___ with eventual ___. Presents with __ or __.

A

atherosclerosis (high pressure on vessel causes inc risk of atherosclerosis); smooth muscle; pulmonary; intimal fibrosis; Plexiform lesions; RV hypertrophy; cor pulmonale; exertional dyspnea; right-sided HF

78
Q

Primary pulmonary HTN is classically seen in ___. Etiology is ___. Some familial forms are related to activating/inactivating mutations of ___, leading to proliferation of ___.

A

young adult females; unknown; inactivating; BMPR2; vascular smooth muscle (thickens the vessel wall leading to HTN)

79
Q

Name 3 causes of secondary pulmonary HTN

A

1) hypoxemia (eg COPD and interstitial lung disease); 2) increased volume in pulmonary circuit (congenital heart disease - can then lead to Eisenmenger syndrome where shunt gets reversed from R to L due to high pHTN); 3) recurrent pulmonary embolism

80
Q

Name 2 respiratory distress syndromes

A

1) acute respiratory distress syndrome (ARDS); 2) neonatal respiratory distress syndrome

81
Q

Acute respiratory distress syndrome (ARDS) is diffuse damage to the ___. It leads to a leakage of ___-rich fluid, which leads to ___ that combines with necrotic ___ to form ___ in alveoli.

A

alveolar-capillary interface (diffuse alveolar damage); protein; edema; epithelial cells; hyaline membranes

82
Q

ARDS can cause __ and __ with respiratory ___, due to thickened ___ and ___ of air sacs (increased/decreased surface tension). ___ is seen on chest X-ray.

A

hypoxemia; cyanosis; distress; diffusion barrier; collapse; increased; white out

83
Q

ARDS is secondary to a variety of disease processes. Name 9. The common theme is activation of __ induces __ and __ mediated damage of type I/type II pneumoncytes.

A

sepsis, infection, shock, trauma, aspiration, pancreatitis, DIC, hypersensitivity rxns, drugs; neutrophil; protease and free radical; both

84
Q

Treatment of ARDS is to address ___. Also __ with ___. Recovery may be complicated by ___, since damage and loss of ___ leads to __ and __

A

underlying cause; ventilation with positive end expiratory pressure (PEEP - need PEEP to keep lungs open after expiration); fibrosis; type II pneumocytes (they are the stem cells); scarring; fibrosis

85
Q

Collapsing pressure (P) =

A

2(surface tension)/(radius); i.e. decreasing surface tension, by increasing surfactant production, decreases collapsing pressure

86
Q

Neonatal respiratory distress syndrome is respiratory distress due to ___. Surfactant is made by ___, and ___ is the major component. Surfactant increases/decreases surface tension in the lung, causing/preventing collapse of alveolar air sacs after expiration.

A

inadequate surfactant levels; type II pneumocytes; phosphatidylcholine (aka lecithin); decreases; preventing

87
Q

Lack of surfactant in the lungs leads to ___ of air sacs and formation of ___.

A

collapse; hyaline membranes

88
Q

Name 3 conditions associated with neonatal respiratory distress syndrome

A

1) prematurity; 2) c-section delivery (due to lack of stress induced steroids, which normally increase synthesis of surfactant); 3) maternal diabetes (insulin decreases surfactant production)

89
Q

Surfactant production begins at ___, and adequate levels are not reached until ___. Amniotic fluid lecithin:___ ratio is used to screen for lung maturity. ___ levels increase as surfactant is produces, and __ remains constant, so a ratio greater than __ indicates adequate surfactant production

A

28 wks; 34 wks; sphingomyelin; lecithin; sphingomyelin; 2 (L:S ratio)

90
Q

Name 4 clinical features of neonatal respiratory distress syndrome. ___ of the lung (‘___’ appearance) is seen on xray.

A

1) increasing respiratory effort after birth; 2) tachypnea with use of accessory muscles; 3) grunting; 4) hypoxemia with cyanosis; diffuse granularity; ground-glass

91
Q

Complications of neonatal respiratory distress syndrome include ___, increasing the risk for persistence of __. Also ___. ___ increases the risk for free radical injury. ___ injury leads to blindness. Lung damage leads to ____.

A

hypoxemia; patent ductus arteriosus; necrotizing enterocolitis (decreased oxygen going to gut); supplemental oxygen; retinal; bronchopulmonary dysplasia

92
Q

What is the most common cause of cancer mortality in the US and what is the average age at presentation? What is the most common cancer incidence in the US?

A

lung cancer; 60; breast/prostate (lung cancer has 2nd highest incidence)

93
Q

Name 3 key risk factors for lung cancer

A

1) cigarette smoke; 2) radon; 3) asbestos (which causes lung cancer more frequently than it causes mesothelioma)

94
Q

Cigarette smoke contains over __ carcinogens. __% of lung cancer occurs in smokers. ___ and __ are particularly mutagenic. Cancer risk is directly related to __ and __ of smoking (‘__’)

A

60; 85; polycyclic aromatic hydrocarbons; arsenic; duration; amount; pack years

95
Q

Radon is formed by ___ decay of __, which is present in the ___. It accumulates in closed spaces such as __. It is responsible for most of the public exposure to ___. It is the ___ most frequent cause of lung carcinoma in the US

A

radioactive; uranium; soil; basements; ionizing radiation; 2nd

96
Q

Lung cancer presenting symptoms are ___ (name 4).

A

nonspecific; cough, weight loss, hemoptysis, post obstructive pneumonia

97
Q

Imaging of lung cancer often reveals a ___ (‘___’). __ is necessary for diagnosis of cancer.

A

solitary nodule; coin-lesion; biopsy

98
Q

Benign lung lesions, which often occur in older/younger patients, can also produce a ‘coin-lesion.’ Name 2 examples

A

younger (less than 40); 1) granuloma (often due to TB or fungus (especially Histoplasma in the Midwest); 2) bronchial hamartoma (benign tumor composed of lung tissue and cartilage; often calcified on imaging)

99
Q

A granuloma in the lung is often due to __ or __ (especially ___ in the midwest). ___ is a benign tumor composed of lung tissue and cartilage. It is often ___ on imaging.

A

TB; fungus; histoplasma; bronchial hamartoma; calcified (a hamartoma is a benign mass comprised of tissue that normally belongs there, but is disorganized)

100
Q

Lung carcinoma is classically divided into these 2 categories. What are the tx differences

A

1) small cell carcinoma (15%) - usually not amenable to surgery, and tx with chemo; 2) non-small cell carcinoma (85%) - upfront surgical resection (does not respond well to chemo)

101
Q

Name the 4 subtypes of NSCLC and their percentages

A

1) adenocarcinoma (40%); 2) squamous cell carcinoma (30%); 3) large cell carcinoma (10%); 4) carcinoid tumor (5%)

102
Q

What is the most common lung cancer tumor in male smokers? female smokers? non-smokers?

A

squamous cell carcinoma; adenocarcinoma; adenocarcinoma

103
Q

Small cell carcinoma is well/poorly differentiated small cells that arises from ___. Associated with ___. Found centrally/peripherally. Rapid/slow growth and early/late mets. What is special about them?

A

poorly; neuroendocrine (Kulchitsky) cells; male smokers; centrally; rapid; early; causes paraneoplastic syndromes: may produce ADH or ACTH or cause Eaton-Lambert syndrome

104
Q

Name 2 histological features of squamous cell carcinoma. Associated with ___. Found centrally/peripherally. May produce ___, causing ___.

A

keratin pearls; intercellular bridges; male smokers; central; PTHrP (parathyroid hormone related peptide); hypercalcemia

105
Q

Name 2 histological features of adenocarcinoma. Associated with ___. Found centrally/peripherally.

A

glands or mucin; most common tumor in non-smokers and female smokers; peripheral

106
Q

Large cell carcinoma are well/poorly differentiated large cells. Associated with ___. Found centrally/peripherally. Excellent/poor prognosis.

A

poorly; smoking; central or peripheral; poor

107
Q

Bronchioloalveolar carcinoma are __ cells that grow along preexisting __ and ___. Arise from __ cells. Associated with ___. Found centrally/peripherally. May present with ___ on imaging. Excellent/poor prognosis

A

columnar; bronchioles; alveoli; Clara cells; not related to smoking!; peripheral; pneumonia-like consolidation; excellent

108
Q

Carcinoid tumor is well/poorly differentiated ___ cells, that are ___ positive. Associated with ___. Found centrally/peripherally (when __, classically forms a ___ mass in the ___). High/low grade malignancy. Rarely can cause ___ syndrome.

A

well; neuroendocrine; chromogranin (cells contain granules that stain chromogranin positive); not related to smoking!; both; central; polyp-like; bronchus; low; carcinoid

109
Q

Name the 2 most common sources of metastasis to the lung. They form multiple ‘___’ nodules on imaging. More/less common than primary lung tumors.

A

breast; colon; cannon-ball; more

110
Q

In lung cancer TNM staging, T is for __ and __. N is for ___ (especially __ and __) and M is for ___. The unique site of metastasis for lung cancer is the ___. Overall, __% 5-year survival. It often presents early/late due to presence/absence of effective screening method

A

tumor size; local extension; spread to regional LNs; hilar and mediastinal; distant metastases; adrenal gland; 15; late; absence

111
Q

Name 4 complications of lung cancer

A

1) pleural involvement; 2) SVC obstruction (SVC syndrome); 3) involvement of recurrent laryngeal nerve (hoarseness) or phrenic (diphragmatic paralysis) nerve; 4) Horner syndrome

112
Q

In lung cancer, pleural involvement is classically seen with ___. Obstruction of the SVC leads to distended __ and __ veins with __ and __ discoloration of __ and __.

A

adenocarcinoma; head and neck; edema; blue; arms; face

113
Q

In lung cancer, compression of the __ leads to Horner syndrome characterized by these 3. Usually due to an __ (___) tumor

A

sympathetic chain; ptosis, miosis, anhidrosis; apical; Pancoast

114
Q

Pneumothorax is an accumulation of __ in the __. Can be __ or __. Which one is a medical emergency?

A

air; pleural space; spontaneous; tension; tension

115
Q

Which type of lung cancers are central? peripheral? both

A

central: SCLC, SCC; peripheral: adenocarcinoma, bronchioloalveolar carcinoma; both: large cell carcinoma, carcinoid tumor

116
Q

Spontaneous pneumothorax is due to ___. Seen in old/young adults. Results in ___ of a portion of the lung. Trachea shifts to the side of/opposite side of collapse.

A

rupture of an emphysematous bleb; young; collapse; side of

117
Q

Tension pneumothorax is due to ___. Air enters the __, but cannot ___. Trace shifts to the side of/opposite side of injury. It is a medical emergency and is treated with ___.

A

penetrating chest wall injury; pleural space; exit; opposite side (pushed there by the entering air); insertion of a chest tube

118
Q

Mesothelioma is a benign/malignant neoplasm of ___ cells. Highly associated with occupational exposure to ___. Presents with recurrent ___, ___, and ___. Tumor encases the lung.

A

malignant; mesothelial; asbestos; pleural effusions; dyspnea; chest pain

119
Q

___ is a rare interestitial lung disease that occurs in women of childbearing age. It is characterized by widespread abnormal proliferation of smooth muscle in the lung, mediastinal and retroperiotneal lymph nodes and major lymphatic ducts. ___ therapy has shown some promise

A

lymphangioleiomyomatosis; hormonal ablation and antiestrogen and progesterone therapy