Cystic fibrosis chest x ray: Difference between revisions

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{{CMG}}; {{AE}} {{SHH}}
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==Overview==
==Overview==
The chest radiographic features may overlap with many other disorders, particularly those characterized by inflammatory or destructive changes of the airways. Atelectasis (especially in right upper lobe) is common in infancy. Most patients with CF demonstrate some of the classic chest radiographic findings that reflect chronic bronchiectasis include hyperinflation, bronchial thickening and dilatation, peribronchial cuffing, mucoid impaction, cystic radiolucencies, increase in interstitial marking and cattered nodular densities.


==X Ray==
==X Ray==
* In cystic fibrosis chest radiographs may be normal early in life.
* In cystic fibrosis chest radiographs may be normal early in life.
* The chest radiographic features overlap with many other disorders, particularly those characterized by inflammatory or destructive changes of the airways.
* The chest radiographic features may overlap with many other disorders, particularly those characterized by inflammatory or destructive changes of the airways.
* Hyperinflation due to mucus plugging of small bronchioles is the earlist radiographic sign of cystic fibrosis in infants and children.
* Hyperinflation due to mucus plugging of small bronchioles is the earlist radiographic sign of cystic fibrosis in infants and children.
* Atelectasis (especially in right upper lobe) is common in infancy.<ref name="pmid24605255">{{cite journal |vauthors=Odev K, Guler I, Altinok T, Pekcan S, Batur A, Ozbiner H |title=Cystic and cavitary lung lesions in children: radiologic findings with pathologic correlation |journal=J Clin Imaging Sci |volume=3 |issue= |pages=60 |date=2013 |pmid=24605255 |pmc=3935260 |doi=10.4103/2156-7514.124087 |url=}}</ref>
* Atelectasis (especially in right upper lobe) is common in infancy.<ref name="pmid24605255">{{cite journal |vauthors=Odev K, Guler I, Altinok T, Pekcan S, Batur A, Ozbiner H |title=Cystic and cavitary lung lesions in children: radiologic findings with pathologic correlation |journal=J Clin Imaging Sci |volume=3 |issue= |pages=60 |date=2013 |pmid=24605255 |pmc=3935260 |doi=10.4103/2156-7514.124087 |url=}}</ref>

Revision as of 14:37, 6 March 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]

Overview

The chest radiographic features may overlap with many other disorders, particularly those characterized by inflammatory or destructive changes of the airways. Atelectasis (especially in right upper lobe) is common in infancy. Most patients with CF demonstrate some of the classic chest radiographic findings that reflect chronic bronchiectasis include hyperinflation, bronchial thickening and dilatation, peribronchial cuffing, mucoid impaction, cystic radiolucencies, increase in interstitial marking and cattered nodular densities.

X Ray

  • In cystic fibrosis chest radiographs may be normal early in life.
  • The chest radiographic features may overlap with many other disorders, particularly those characterized by inflammatory or destructive changes of the airways.
  • Hyperinflation due to mucus plugging of small bronchioles is the earlist radiographic sign of cystic fibrosis in infants and children.
  • Atelectasis (especially in right upper lobe) is common in infancy.[1]
  • Most patients with CF demonstrate some of the classic chest radiographic findings that reflect chronic bronchiectasis:[2]
    • Hyperinflation
    • Bronchial thickening and dilatation
    • Peribronchial cuffing
    • Mucoid impaction
    • Cystic radiolucencies
    • Increase in interstitial markings
    • Scattered nodular densities

References

  1. Odev K, Guler I, Altinok T, Pekcan S, Batur A, Ozbiner H (2013). "Cystic and cavitary lung lesions in children: radiologic findings with pathologic correlation". J Clin Imaging Sci. 3: 60. doi:10.4103/2156-7514.124087. PMC 3935260. PMID 24605255.
  2. Grum CM, Lynch JP (September 1992). "Chest radiographic findings in cystic fibrosis". Semin Respir Infect. 7 (3): 193–209. PMID 1475543.

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