|
|
||||||||
American Journal of Roentgenology, Vol 173, 1583-1588, Copyright © 1999 by American Roentgen Ray Society
ARTICLES |
CJ Chung, LA Fordham, P Barker and LL Cooper
Department of Radiology, University of North Carolina School of Medicine, Chapel Hill 27599-7510, USA.
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.
This article has been cited by other articles:
![]() |
P.M. Barker, C.R. Esther Jr, L.A. Fordham, S.J. Maygarden, and W.K. Funkhouser Primary pulmonary lymphangiectasia in infancy and childhood Eur. Respir. J., September 1, 2004; 24(3): 413 - 419. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Finder, J. Steinfeld, T. M. Berger, C. Hagmann, and J.-O. Gebbers Congenital Pulmonary Lymphangiectasia N. Engl. J. Med., February 26, 2004; 350(9): 948 - 948. [Full Text] [PDF] |
||||
![]() |
R. Soferman, H. Mussaffi, L. Schreiber, H. Nagar, and Y. Sivan Congenital Pulmonary Lymphangiectasis Clinical Pediatrics, November 1, 2003; 42(9): 831 - 834. [PDF] |
||||
![]() |
S. Y. Lee, S. R. Yang, and K. R. Lee Congenital Pulmonary Lymphangiectasia With Chylothorax Asian Cardiovasc Thorac Ann, March 1, 2002; 10(1): 76 - 77. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |