Morgagni hernia

Basit Öğe Kaydı
dc.authoridÜstün, Nuran/0000-0003-1680-1825
dc.authoridKutlu, Nurettin Onur/0000-0002-3306-6570
dc.authoridsoylu, hikmet/0000-0003-4118-366X
dc.authorwosidÜstün, Nuran/AAE-6740-2019
dc.authorwosidKutlu, Nurettin Onur/AAW-6196-2021
dc.authorwosidsoylu, hikmet/M-8019-2018
dc.contributor.authorSoylu, H
dc.contributor.authorKoltuksuz, U
dc.contributor.authorKutlu, NO
dc.contributor.authorSarihan, H
dc.contributor.authorSen, Y
dc.contributor.authorÜstün, N
dc.contributor.authorBaki, A
dc.date.accessioned2024-08-04T20:12:07Z
dc.date.available2024-08-04T20:12:07Z
dc.date.issued2000
dc.departmentİnönü Üniversitesien_US
dc.description.abstractMorgagni hernia (MH) is the least common type of congenital diaphragmatic hernias. Although its course is often asymptomatic, it may be associated with various respiratory and gastrointestinal symptoms. We describe 7 children with MH during a 5-year period in three pediatric centers in Turkey. All children had acute or chronic respiratory symptoms; cough was the most frequent. The diagnosis was made by posterior-anterior (PA) and lateral chest X-rays. The PA chest X-rays showed a homogenous mass in 2 and a gas-filled cystic image in 3 children in the right cardiophrenic angle. A retrocardiac homogeneous density in one child, and bilateral consolidation in lower lung areas in another child were also seen. All lateral chest X-rays showed gas-filled bower loops above the diaphragm. The diagnosis was confirmed by barium-contrast radiograph. Four patients had five additional anomalies, i.e., ventricular septal defect, right inguinal hernia, congenital hip dislocation, pectus carinatum, and obstruction of the uretero-pelvic junction. All of the hernias were repaired by an abdominal approach. There were no complications or recurrences during follow-up. In conclusion, MH should be considered in the differential diagnosis of cases of long-standing respiratory symptoms and/or when an unexplained radiological image, especially on the right cardiophrenic area, is present. (C) 2000 Wiley-Liss, Inc.en_US
dc.identifier.doi10.1002/1099-0496(200011)30:5<429
dc.identifier.endpage433en_US
dc.identifier.issn8755-6863
dc.identifier.issue5en_US
dc.identifier.pmid11064435en_US
dc.identifier.scopus2-s2.0-0033626444en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage429en_US
dc.identifier.urihttps://doi.org/10.1002/1099-0496(200011)30:5<429
dc.identifier.urihttps://hdl.handle.net/11616/93205
dc.identifier.volume30en_US
dc.identifier.wosWOS:000090118200010en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherWiley-Lissen_US
dc.relation.ispartofPediatric Pulmonologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectdiaphragmatic herniaen_US
dc.subjectMorgagni herniaen_US
dc.subjectrespiratory systemen_US
dc.subjectchest massen_US
dc.subjectcongenital anomaliesen_US
dc.subjectchildhooden_US
dc.titleMorgagni herniaen_US
dc.typeArticleen_US

Dosyalar

Koleksiyon

WoS İndeksli Yayınlar Koleksiyonu
PubMed İndeksli Yayın Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu