Pulm 6/17 Quiz Review Flashcards
Lung CA:
define pulmonary nodule
Lung CA
= small opacities,
less than 3 cm in size
Notes:
usually asymptomatic
usually detected incidentally
or at time of screening
Lung CA:
define lung mass
Lung CA
= any opacity larger than 3 cm in size
Notes:
malignant until proven otherwise
Lung CA:
two primary categories of Lung CA are:
Lung CA
- non small cell lung cancer (NSCLC)
- small cell lung cancer (SCLC)
Lung CA:
growth rate of small cell lung cancer (SCLC) =
Lung CA
grow very very fast
Lung CA:
who predominantly gets SCLC?
Lung CA
```
smokers do
“occur predominantly in smokers”
~~~
Lung CA:
what are the two stages of SCLC? How are they defined?
Lung CA
Limited Stage & Extensive Stage
Limited Stage = all disease w/in single radiation field (i.e. single hemithorax, possibly with some supraclavicular lymph nodes thrown in)
Extensive Stage = disease OUTSIDE a single hemithorax
Lung CA:
what is the most common non-small cell lung cancer (NSCLC)?
Lung CA
adenocarcinoma
Lung CA:
what is the TNM system of staging? What does TNM stand for?
Lung CA
T = tumor N = node M = metastasis
I = solitary tumor, tumor <= 4 cm, no lymph node involvement
II = tumor > 4 cm, regional lymph nodes involved, invasion into local structures
III = medistinal lymph nodes positive
IV = distant metastatic disease (includes pleural effusion)
Lung CA:
how to treat lung cancers at different stages –>
Lung CA
FIRST = biopsy, determine if NSCLC or SCLC!
I - surgical resection
II - surgical resection + chemo
III = chemoradiation
IV = palliative care (incurable)
Lung CA:
name some NSCLC presentations
Lung CA
hyperalcemia
hypertrophic pulm osteoarthropathy (NOT finger clubbing)
inflammatory myopathies
Lung CA:
what is most common subtype of lung cancer?
Lung CA
NON-small cell lung cancer (NSCLC)
Lung CA:
common symptoms for lung cancer = ?
Lung CA
typical: cough, increased sputum, shortness of breath
common: fatigue, wt loss, anorexia, low-grade fever
Lung CA:
name some SCLC presentations
Lung CA
paraneoplastic syndromes: hyponatremia (SIADH) hypertrophic pulm osteoathropathy (NOT finger clubbing, same as NSCLC) inflammatory myopathies (same as NSCLC) Cushing Syndrome Lambert-Eaton syndrome cerebellar degeneration
CF Dx/Trtmt: Epi
What ethnicity carries highest rates of cystic fibrosis?
CF Dx/Trtmt: Epi
Caucasian
CF Dx/Trtmt: Dx approach, newborn screening:
To dx CF, pt must have at least one of these three symptoms:
CF Dx/Trtmt: Dx approach, newborn screening
>1 typical phenotypic features of CF sibling with CF positive newborn screening test
CF Dx/Trtmt: Dx approach, newborn screening:
To dx CF, pt must ALSO have one of these three symptoms (in addition to the three required):
CF Dx/Trtmt: Dx approach, newborn screening
- elevated sweat chloride on 2 occasions - TWO disease-causing CFTR mutations = abnormal nasal potential difference
CF Dx/Trtmt: Dx approach, newborn screening:
Why is newborn screening helpful/important?
CF Dx/Trtmt: Dx approach, newborn screening
“With widespread adoption of newborn screening in recent years, we have seen a….an increasing number of infants diagnosed before a month of age”
CF Dx/Trtmt: Dx approach, newborn screening:
Three most common phenotypical symptoms seen in CF diagnoses
CF Dx/Trtmt: Dx approach, newborn screening
acute/persistent respiratory symptoms (37.3%)
steatorrhea (22.4%)
meconium ileus/intestinal obstruction (17.6%)
CF Dx/Trtmt: Dx approach, newborn screening:
What is the GOLD STANDARD For CF dx?
CF Dx/Trtmt: Dx approach, newborn screening
SWEAT CHLORIDE TESTING (done at an accredited CF Care Center)
CF Dx/Trtmt: Dx approach, newborn screening:
What is required for a positive genetic test for CF?
CF Dx/Trtmt: Dx approach, newborn screening
“TWO defective genes in trans configuration”
CF Dx/Trtmt: Dx approach, newborn screening:
What is the most common mutation for CF?
CF Dx/Trtmt: Dx approach, newborn screening
F508del (70% of mutations)
CF Dx/Trtmt: Dx approach, newborn screening:
How do we test newborns for CF?
CF Dx/Trtmt: Dx approach, newborn screening
We check for immunoreactive trypsinogen
(this is an exocrine pancreatic protein, which is elevated in newborns with CF (3-5 x higher))
CF Dx/Trtmt: CF pathophys:
Describe CFTR
CF Dx/Trtmt: CF pathophys
what is it? gene
location: long arm of chromosome 7
function: codes for protein in cell membrane of many organs
action: acts as chloride channel
(also controls other channels)
CF Dx/Trtmt: CF pathophys:
name three basic symptoms of CFTR mutation
CF Dx/Trtmt: CF pathophys
GI
Upper Respiratory System
Lower Respiratory System