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Journal

2011 | 6 | 1 | 131-135

Article title

Congenital herniation through the foramen Morgagni - clinical presentation, diagnosis and treatment in pediatric population

Content

Title variants

Languages of publication

EN

Abstracts

EN
Congenital Morgagni hernia is a rare entity, accounting for less than 1,5% of all types of congenital diaphragmatic hernias. The majority of Morgagni hernias are diagnosed late because patients can be asymptomatic or present with non-specific respiratory and gastrointestinal symptoms and signs. The medical records of all patients diagnosed with CMH and treated in our hospital were retrospectively reviewed for age at diagnosis, sex, site of hernia, clinical symptoms, associated anomalies, operative findings and treatment. Over a 20-year period, 5 cases with CMH diagnoses were hospitalized and operated. The age of diagnosis ranged from nine months to 11 years. Male to female ratio was 3:2. Associated anomalies were seen in 2 patients (40%). Most patients had transabdominal operations. There were no complications in the postoperative period. Morgagni hernia is a rare condition. The rarity is due to the nonspecific presentation of symptoms, which contributes to a delay in diagnosis. We advocate surgical repair even in asymptomatic patients, because of the risk of strangulation. There is a low rate of complications.

Publisher

Journal

Year

Volume

6

Issue

1

Pages

131-135

Physical description

Dates

published
1 - 2 - 2011
online
16 - 12 - 2010

Contributors

  • Pediatric Surgery Clinic, 18000, Niš, Serbia
  • Pediatric Surgery Clinic, 18000, Niš, Serbia
  • Pediatric Surgery Clinic, 18000, Niš, Serbia
  • Pediatric Surgery Clinic, 18000, Niš, Serbia
author
  • Department of Anestesiology, Pediatric Surgery Clinic, 18000, Niš, Serbia

References

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  • [13] Richardson WS, Bolton JS. Laparoscopic repair of congenital diaphragmatic hernias. J Laparoendosc Adv Surg Tech A 2002;12(4):277–280 http://dx.doi.org/10.1089/109264202760268078[Crossref]
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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11536-010-0061-2
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