Congenital diaphragmatic hernia associated with uncommon abnormalities
Introduction: Congenital diaphragmatic hernia is a poor forma - tion of the diaphragm characterized by the presence of an intestinal malrotation, It is related to abnormal position of the intestine in the thorax. Objective and Result: This case report a stillborn at 32 weeks, that was observe anatom...
| Autores: | , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2017 |
| País: | Brasil |
| Institución: | Universidade Federal do Ceará (UFC) |
| Repositorio: | Repositório Institucional da Universidade Federal do Ceará (UFC) |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.ufc.br:riufc/23480 |
| Acceso en línea: | http://www.repositorio.ufc.br/handle/riufc/23480 |
| Access Level: | acceso abierto |
| Palabra clave: | Hérnia Hérnias Diafragmáticas Congênitas Hernias, Diaphragmatic, Congenital |
| Sumario: | Introduction: Congenital diaphragmatic hernia is a poor forma - tion of the diaphragm characterized by the presence of an intestinal malrotation, It is related to abnormal position of the intestine in the thorax. Objective and Result: This case report a stillborn at 32 weeks, that was observe anatomical abnormalities associated with congenital dia - phragmatic hernia, which occurred in the left antero-posterior region, such as intestinal malrotation, hepatomegaly and nephromegaly, with the presence of a hernial ring that occupied 80% of the left side of the diaphragm, besides a hypertrophied heart, deviated to the right, bilateral pulmonary hypotrophy. Conclusion This case illustrates a rare case of diaphragmatic hernia with intestinal changes of clinical and surgical importance. |
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