Journal of Pediatric Surgery
Volume 40, Issue 12 , Pages 1839-1843, December 2005

Late-presenting congenital diaphragmatic hernia

  • By the Congenital Diaphragmatic Hernia Study Group

      Affiliations

    • Corresponding Author InformationCorresponding author. Yoshihiro Kitano, Division of General Surgery at National Center for Child Health and Development, Tokyo 157-8535 Japan.
    • The members of the Congenital Diaphragmatic Hernia Study Group are listed in the appendix.

Abstract 

Background

Late-presenting congenital diaphragmatic hernia (CDH) is a rare subset of CDH, most of the information derived from small series or case reports. The aim of this study was to document the clinical manifestations of late-presenting CDH using a large multicenter database.

Methods

Information about late-presenting CDH (diagnosed at later than 30 days of age) was identified from the database of the CDH Study Group (3098 cases collected during 1995-2004) and reviewed retrospectively.

Results

Seventy-nine cases (2.6%) from 30 centers met the inclusion criteria. Seven cases had a Morgagni hernia. There were 50 males (65%) and 27 females (35%). The mean age at diagnosis was 372 days (32 days to 15 years). Major associated anomalies (10 cardiac and 7 chromosomal abnormalities) were identified in 12 cases (15%). Presenting symptoms were respiratory in 20 (43%), gastrointestinal in 15 (33%), both in 6 (13%), and none (asymptomatic) in 5 (11%). The hernia was left-sided in 53 (69%), right-sided in 21 (27%), and central or bilateral in 3 (4%). Patients with gastrointestinal symptoms invariably had left-sided hernias (n = 19), whereas patients with respiratory symptoms (n = 24) seemed equally likely to have right- or left-sided lesions. A primary repair without patch was done in all cases with 100% survival.

Conclusions

Presenting symptoms of late-onset CDH can be respiratory or gastrointestinal, but presentation with gastrointestinal problems was more common in left-sided hernias, whereas respiratory symptoms predominated in right-sided lesions. The prognosis is excellent once the correct diagnosis is made.

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 Presented at the 38th Annual Meeting of the Pacific Association of Pediatric Surgeons, May 22-26, 2005, Vancouver, Canada.

 The writing committee for the Congenital Diaphragmatic Hernia Study Group (Yoshihiro Kitano, National Center for Child Health and Development, Tokyo Japan; Kevin P. Lally and Pamela A. Lally, University of Texas–Houston, Houston, Tex) takes responsibility for the content of this article.

PII: S0022-3468(05)00680-9

doi:10.1016/j.jpedsurg.2005.08.023

Journal of Pediatric Surgery
Volume 40, Issue 12 , Pages 1839-1843, December 2005