Literature DB >> 10584805

Children with congenital pulmonary lymphangiectasia: after infancy.

C J Chung1, L A Fordham, P Barker, L L Cooper.   

Abstract

OBJECTIVE: The objective of this original report is to describe the characteristic chest imaging findings in children with primary congenital pulmonary lymphangiectasia who survive infancy.
CONCLUSION: In children with primary congenital pulmonary lymphangiectasia, increased interstitial markings decrease over time and increased hyperinflation is associated with persistent patchy areas of ground-glass opacity.

Entities:  

Mesh:

Year:  1999        PMID: 10584805     DOI: 10.2214/ajr.173.6.10584805

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  5 in total

1.  Imaging of Childhood Interstitial Lung Disease.

Authors:  R Paul Guillerman
Journal:  Pediatr Allergy Immunol Pulmonol       Date:  2010-03       Impact factor: 1.349

2.  Pediatric lymphangiectasia: an imaging spectrum.

Authors:  Ladonna J Malone; Laura Z Fenton; Jason P Weinman; Miran R Anagnost; Lorna P Browne
Journal:  Pediatr Radiol       Date:  2014-10-10

3.  Case Report: A Relatively Mild Presentation of Unilateral Congenital Pulmonary Lymphangiectasia.

Authors:  Dionne Adair; Raja Rabah; Maria Ladino-Torres; Thomas G Saba
Journal:  Front Pediatr       Date:  2021-04-22       Impact factor: 3.418

Review 4.  HRCT in paediatric diffuse interstitial lung disease--a review for 2009.

Authors:  Maria Klusmann; Catherine Owens
Journal:  Pediatr Radiol       Date:  2009-06

Review 5.  Congenital pulmonary lymphangiectasia.

Authors:  Carlo Bellini; Francesco Boccardo; Corradino Campisi; Eugenio Bonioli
Journal:  Orphanet J Rare Dis       Date:  2006-10-30       Impact factor: 4.123

  5 in total

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