Respiratory- CA, CF, Failure Flashcards

1
Q

Describe the Characteristics of Lung CA

character and spread

A
  • 1* and 2*
  • major cause of death
  • aggressive, invasive, metastatic
  • spreads to bone, liver and brain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Describe 4 types of Lung CA and incidence

A
o  Adenocarcinomas (~30%)
o  Squamous cell carcinoma (30%)
 (Non-Small Cell Lung Cancer)
o  Large cell carcinoma (~12%)
o  Small cell carcinoma (~22%) SCLC
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Etiology of lung CA (risks)

A

• Smoking (>80%)
• Toxins (eg asbestos)
• Genetic predisposition
(…HLA on 6 plus other familial connections)

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

Describe Adenocarcinoma

A

Peripheral origin
(Alveoli or bronchioles)

Common in women (not clear why) and in non smoker (not clear why)

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

Describe squamous cell carcinoma

A

o Arises in the central bronchi (hilum)
o Spreads to hilar nodes
o More common in men (no clear reason)
o Growth can effect external structures like the heart.

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

Describe Large cell carcinoma

A

o Peripheral origin
(Alveoli and bronchioles)
o Large and undifferentiated cells
o Early metastasis (Poor prognosis)

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

Describe Small cell carcinoma

A
o	99% in smokers
o	Aggressive, invasive, early metastasis (esp brain)
o	Small, oval cells
o	Often metastasized by Dx 
o	Non-resectable
o	Radiosensitive

plus paraneoplastic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Which type of CA is related to paraneoplastic syndrome?

A

Small cell carcinoma

Paraneoplastic refers to ectopic tumors we spoke of in endocrine

(eg SIADH, Cushings – cortico and ACTH excess)

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

MNFTS of lung CA

A
  • Based on type and location (eg. Central or peripheral- bronchi, lungs, heart)
  • Based on extent and metastasis
  • Paraneoplastic syndromes

• For all types/locations
o Hemoptysis
o Pain

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

What sort of MNFTS are dependent of location of tumor in lung CA

A

If central -> impairs ventilation -> coughing, wheezing, dyspnea

Tumors on left side will result in cardiac MNFTS

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

Dx of Lung CA

A
  • Hx, Px, US, CXR, MRI
  • Bronchoscopy, needle biopsy
  • Cytology (sputum or bronchial wash)

No adequate screen to pick up early lung cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Tx for Lung CA

A
  • NSCLC: Sx, radiation and chemo
  • SCLC: chemo and radiation
  • Poor prognosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is Cystic Fibrosis

A

Hereditary exocrine disease

Defective Cl- channel in cell membrane leading to hypersecretion (or at least build up) of fluid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What systems does cystic fibrosis Affect?

A

Exocrine cells!

GI tract (pancreas, etc), reprod tract and resp system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Etiology of Cystic Fibrosis

A

•CFTR (cystic fibrosis transmembrane regulator) gene on Chr 7

(CFTR is the protein)

Autosomal recessive

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

Patho of Cystic Fibrosis

A

CFTR gene mutation leads to defective Cl channel on epith cells of resp tract (and elsewhere)

• Mutation makes cell impermeable to Cl-
leading to Impaired Cl- transport across cell membrane

  • Abnormal secretion and also inc concentration of Cl- on outside of epithelial membrane
  • High Cl- conc pulls h20 and Na from mucous in the resp. lumen
  • Mucous becomes thick and viscous cannot be moved by cilia -> dec cilliary fx -> plugs airway -> dec fx (i.e gas exchange)
  • Mucous is great spot for bact growth (recurrent bacterial infection.
  • > 90% die from severe pulmonary disease
17
Q

Dx of cystic Fibrosis

A
  • Sweat test
  • CF in a sibling
  • Newborn (trypsinogen) = a precursor for trypsin
  • GI and Resp tract MNFTS
18
Q

Tx of Cystic Fibrosis?

A

• No cure, will succumb to respiratory failure (inflm and inf)

• DNAase (reduce mucus stickiness)
o DNA released by dead cells in mucus, help reduce strands making it easier to mobilize

• Control infection (they tend to be major and persistent)
o Prophylaxis, and abx tx, not easy
• Diet mod and pancreatic E supplement
• Anti inflm and gamma globulins indications)

19
Q

What is Respiratory Failure?

A

•No gaseous exchange

o Hypoxemia and Hypercapnea

20
Q

Tx of Respiratory Failure

A
• Restore gas exchange eg:
   o 02
   o Bronchodilators ?? (based on cause)
   o Mech ventilation`
   o Abx?? (based on cause)
21
Q

MNFTS of Respiratory Failure

A

Hypercapnia ( over 45mmHG)
Hypoxemia (under 60mmHG)
Resp Acidosis
MNFTS of Cause