Cystic fibrosis chest x ray: Difference between revisions
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* 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> | ||
*Most patients with CF demonstrate some of the classic chest radiographic findings that reflect chronic bronchiectasis:<ref name="pmid1475543">{{cite journal |vauthors=Grum CM, Lynch JP |title=Chest radiographic findings in cystic fibrosis |journal=Semin Respir Infect |volume=7 |issue=3 |pages=193–209 |date=September 1992 |pmid=1475543 |doi= |url=}}</ref> | *Most patients with CF demonstrate some of the classic chest radiographic findings that reflect chronic bronchiectasis:<ref name="pmid1475543">{{cite journal |vauthors=Grum CM, Lynch JP |title=Chest radiographic findings in cystic fibrosis |journal=Semin Respir Infect |volume=7 |issue=3 |pages=193–209 |date=September 1992 |pmid=1475543 |doi= |url=}}</ref><ref name="pmid24065629">{{cite journal |vauthors=Vult von Steyern K, Björkman-Burtscher IM, Geijer M |title=Radiography, tomosynthesis, CT and MRI in the evaluation of pulmonary cystic fibrosis: an untangling review of the multitude of scoring systems |journal=Insights Imaging |volume=4 |issue=6 |pages=787–98 |date=December 2013 |pmid=24065629 |pmc=3846934 |doi=10.1007/s13244-013-0288-y |url=}}</ref> | ||
**Hyperinflation | **Hyperinflation | ||
**Bronchial thickening and dilatation | **Bronchial thickening and dilatation | ||
Revision as of 14:42, 6 March 2018
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Cystic fibrosis chest x ray On the Web |
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American Roentgen Ray Society Images of Cystic fibrosis chest x ray |
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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
In cystic fibrosis the chest radiographic features may overlap with many other disorders, particularly those characterized by inflammatory or destructive changes of the airways. Atelectasis 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][3]
- Hyperinflation
- Bronchial thickening and dilatation
- Peribronchial cuffing
- Mucoid impaction
- Cystic radiolucencies
- Increase in interstitial markings
- Scattered nodular densities
References
- ↑ 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.
- ↑ Grum CM, Lynch JP (September 1992). "Chest radiographic findings in cystic fibrosis". Semin Respir Infect. 7 (3): 193–209. PMID 1475543.
- ↑ Vult von Steyern K, Björkman-Burtscher IM, Geijer M (December 2013). "Radiography, tomosynthesis, CT and MRI in the evaluation of pulmonary cystic fibrosis: an untangling review of the multitude of scoring systems". Insights Imaging. 4 (6): 787–98. doi:10.1007/s13244-013-0288-y. PMC 3846934. PMID 24065629.