Publication: Mediastinal Hemangioma and Accompanying Aortic Arch Anomaly
| dc.contributor.author | Ceyhan, Meltem | |
| dc.contributor.author | Elmali, Muzaffer | |
| dc.contributor.author | Yildiz, Levent | |
| dc.date.accessioned | 2020-06-21T15:13:33Z | |
| dc.date.available | 2020-06-21T15:13:33Z | |
| dc.date.issued | 2008 | |
| dc.department | OMÜ | en_US |
| dc.department-temp | [Ceyhan, Meltem -- Elmali, Muzaffer] Ondokuz Mayis Univ, Fac Med, Dept Radiol, TR-55139 Samsun, Turkey -- [Yildiz, Levent] Ondokuz Mayis Univ, Fac Med, Dept Pathol, TR-55139 Samsun, Turkey -- | en_US |
| dc.description.abstract | Hemangioma is a rare tumor of the mediastinum. There are a very small number of patients identified with a combination of mediastinal hemangioma and aortic arch anomaly in the medical literature review. Here we present a fatal case of a 2-month-old female infant having mediastinal hemangioma compressing the trachea accompanied by a right-sided aortic arch with an aberrant left subclavian artery. | en_US |
| dc.identifier.doi | 10.1007/s00246-007-9192-x | |
| dc.identifier.endpage | 869 | en_US |
| dc.identifier.issn | 0172-0643 | |
| dc.identifier.issue | 4 | en_US |
| dc.identifier.pmid | 18183452 | |
| dc.identifier.startpage | 867 | en_US |
| dc.identifier.uri | https://doi.org/10.1007/s00246-007-9192-x | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/19268 | |
| dc.identifier.volume | 29 | en_US |
| dc.identifier.wos | WOS:000257393800037 | |
| dc.language.iso | en | en_US |
| dc.publisher | Springer | en_US |
| dc.relation.journal | Pediatric Cardiology | en_US |
| dc.relation.publicationcategory | Diğer | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Vascular Anomaly | en_US |
| dc.subject | Mediastinal Hemangioma | en_US |
| dc.subject | Aortic Arch | en_US |
| dc.title | Mediastinal Hemangioma and Accompanying Aortic Arch Anomaly | en_US |
| dc.type | Editorial | en_US |
| dspace.entity.type | Publication |