Pulm pathology prt 2 Flashcards

1
Q

Pleuritic pain is caused by an irritated ___ nerve

A

Phrenic

(C3-4-5) referred to shoulder

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2
Q

Patients with ___ are at increased risk for lung abscess due to the aspiration of oral flora during periods of unconsciousness.

A

alcohol use disorder

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3
Q

The main pathogens of aspiration induced lung abscess are ____ of the oral flora

A

strict and facultative anaerobic

(Bacteroides, Prevotella, Fusobacterium, Peptostreptococcus).

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4
Q

Manifestations include subacute fever, cough, and foul-smelling sputum.

A

aspiration induced lung abscess

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5
Q

Lobar pneumonia is marked by the cytokine-mediated accumulation of neutrophils and _____ material in the alveoli. Over several days, the material becomes fibrinous.
neutrophils are replaced by macrophages, and macrophages digest the fibrinous exudate,
thereby restoring normal lung histology.

A

proteinaceous

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6
Q
bilateral "Velcro"-sounding crackles
Reticular nodular (bright, branching, lines) opacities
A

Pulmonary fibrosis

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7
Q

Lung parenchyma inflammation

Aspiration of gastric acid with direct tissue injury

A

chemical pneumonitis

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8
Q

Periods of altered consciousness (alcoholism, seizures, dementia)

Impaired swallowing (nasogastric tube, dysphagia)

Periodontal disease, particularly gingivitis

Increased risk for

A

Lung abscess from microaspiration

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9
Q

fever, cough productive of copious sputum (often foul-smelling), and chest x-ray evidence of cavitation with air-fluid level.

A

Lung abscess
(microaspiration, untreated pneumonia)
NEUTROPHILS MEDIATE Liquifying necrosis

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10
Q

has a propensity to affect older adults with chronic lung disease who smoke.

It causes high fever, diarrhea, headache, and confusion.

It is a non-staining gram-negative rod diagnosed by PCR

A

Legionella pneumophila

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11
Q

triad of respiratory distress, neurologic dysfunction, and petechial rash that characterizes the condition

A

Fat Embolism

Recent trauma

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12
Q

syndrome commonly presents with chronic fatigue, dyspnea, and difficulty concentrating.

A

Obesity hypoventilation

*OHS results from physical restriction of lung expansion by excessive thoracic tissue mass. Low TV

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13
Q

Loss of intrapleural negative pressure (pneumothorax) causes the chest wall to spring outward & inspiratory compliance is

A

decreased

*Hemithorax increases in volume

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14
Q

Age-related changes to the respiratory system include decreased chest wall compliance and ____ alveolar elastic recoil with resulting alveolar enlargement and air trapping.

A

decreased

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15
Q

Malignancies like adenocarcinoma can cause Pleural effusion due to increased vascular permeability or ___

A

*Lymphatic obstruction

Thoracentesis yields fluid with a large number of red blood cells and numerous atypical cells staining positive for mucin

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16
Q

Pleural fluid normally enters the pleural space via intercostal microvessels of the parietal pleura, and exits the pleural space via

A

parietal pleura lymphatics.

*Visceral pleural fluid comes from bronchial microvessels

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17
Q

Autosomal dominant mutations impairing TGF-β signaling

Disrupted angiogenesis & loss of vascular integrity causing VASCULAR malformation

A

Hereditary Hemorrhagic Telangiectasia

18
Q

telangiectasia
Recurrent nose bleeds
Visceral organ Vascular Malformation:
gastrointestinal tract (bleeding), lung (hemoptysis), brain (hemorrhagic stroke), liver

Complications
High-output heart failure
Pulmonary hypertension
Paradoxic embolism
Iron deficiency anemia
A

Hereditary Hemorrhagic Telangiectasia

19
Q

In the lungs, the binding of O2 to hemoglobin drives the release of ____(2) from hemoglobin (Haldane effect).

A

H+ and CO2

20
Q

In the _____ tissues, high concentrations of CO2 and H+ facilitate O2 unloading from hemoglobin (Bohr effect).

A

peripheral

21
Q

Ciliated epithelium persists up to and ends at the respiratory

A

bronchioles

(Proximal bronchioles → Terminal → Respiratory bronchioles) PTR

22
Q

Terminal bronchiles have ciliated epithelium, serous glands, and

A

club cells

23
Q

After terminal bronchioles are RESPIRATORY bronchioles which have only ciliated cells, club cells and

A

Macrophages

*next comes alveoli which also have MQs

24
Q

Patients who are upright tend to aspirate into the ___ segments of the lower lobes.

A

basilar

25
Q

Supine patients typically aspirate into the ___ segments of the upper lobes and ____ segments of the lower lobes.

A

posterior

superior

26
Q

Ventilation is lowest in the ___ and highest in the ___ because gravity acts to stretch the lungs downward so that the alveoli at the apex are expanded more than those at the base

A

apex

base

27
Q

Perfusion is also lowest in the ___ and highest in the ___, as the increased hydrostatic pressure in the lower lung regions facilitates increased blood flow.

A

apex

base

28
Q

increased extraction of oxygen by skeletal muscle results in _____ mixed venous oxygen content

A

decreased

29
Q

IL-4 causes

A

IgE production

30
Q

IL-5 causes

A

Eosinophil recruitment

31
Q

bronchoconstriction is mediated by the ___ nervous system when the vagus nerve is stimulated (via an inhaled irritant)

A

parasympathetic

32
Q

Supplemental oxygen administration in patients with chronic obstructive pulmonary disease can lead to increased CO2 retention (oxygen-induced hypercapnia), resulting in confusion and depressed consciousness. The major cause is reversal of hypoxic pulmonary vasoconstriction, which increases physiologic dead space as blood is shunted away from well-ventilated alveoli.

A

Arterial partial pressure of carbon dioxide (PaCO2) is the major stimulator of respiration in healthy individuals; even a slight increase in PaCO2 stimulates central chemoreceptors and triggers increased ventilation. In patients with chronic obstructive pulmonary disease, the response to PaCO2 is blunted and hypoxemia can contribute to respiratory drive. Peripheral chemoreceptors are primarily responsible for sensing arterial partial pressure of oxygen (PaO2) and can be suppressed with oxygen administration causing hypoventilation

33
Q

Patients with severe emphysema typically have chronic ____ leading to chronic respiratory acidosis with metabolic compensation and hypoxemia

A

CO2 retention

34
Q

is the predominant substance contained within eosinophilic granules, and it acts as a potent toxin against helminths (parasitic worms).

A

Major basic protein

35
Q
Aspirin/NSAIDs
Nonselective beta blockers
Upper respiratory infection
Exercise & cold, dry air
Gastroesophageal reflux disease
can cause
A

Asthma exacerbation

eosinophilia

36
Q

is a major problem in lung transplant recipients; it affects small airways, causing bronchiolitis obliterans. It is characterized by lymphocytic inflammation, fibrosis, and, ultimately, destruction of the bronchioles.

A

Chronic rejection

37
Q

Thickened bronchial walls, lymphocytic infiltration, mucous gland enlargement, and patchy squamous metaplasia of the bronchial mucosa are features of

A

chronic bronchitis

38
Q

Exposure to high temperature or exercise can lead to hyponatremia and hypochloremia due to excessive sodium chloride loss through sweat; therefore, salt supplementation is recommended.

A

Cystic Fibrosis

39
Q

Vitamin A maintains orderly differentiation of specialized epithelia, including the mucus-secreting columnar epithelia of the ocular conjunctiva, respiratory and urinary tracts, and pancreatic and other exocrine ducts. Avitaminosis A can cause squamous metaplasia of such epithelia to a keratinizing epithelium.

A

Cystic Fibrosis causing Pancreatic Problems

40
Q

This neonate has respiratory distress with asymmetric breath sounds and a scaphoid abdomen, findings concerning for congenital

A
diaphragmatic hernia (CDH)
*causes pulm HYPOplasia
41
Q

In cystic fibrosis, impairment of the cystic fibrosis transmembrane conductance regulator (CFTR) protein reduces chloride secretion and ___ sodium absorption by the respiratory epithelia, resulting in dehydrated mucus.

A

increases

*When saline is applied to the nasal mucosa, the increased sodium absorption in patients with CF causes a more negative nasal transepithelial potential difference

42
Q

This mutation causes impaired post-translational processing (eg, improper folding and glycosylation) of the receptor protein, which is detected by the endoplasmic reticulum. As a result, the abnormal protein is targeted for proteasomal degradation, preventing it from reaching the cell surface. Certain drugs (lumacaftor) can partially correct this folding defect, leading to expression of functional receptor protein on cell surface

A

CFTR

Cystic Fibrosis