| dc.contributor.author | Caglayan, F | |
| dc.contributor.author | Cakmak, M | |
| dc.contributor.author | Bozdogan, O | |
| dc.contributor.author | Abasiyanik, F | |
| dc.date.accessioned | 2020-06-25T17:35:43Z | |
| dc.date.available | 2020-06-25T17:35:43Z | |
| dc.date.issued | 2003 | |
| dc.identifier.citation | closedAccess | en_US |
| dc.identifier.issn | 0041-4301 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12587/3190 | |
| dc.description | WOS: 000182199300014 | en_US |
| dc.description | PubMed: 12718375 | en_US |
| dc.description.abstract | Infantile myofibromatosis presents as a firm, nodular mass in soft tissues, muscles, or visceras which can be solitary or multicentric, and it may regress spontaneously. We present a one-day-old boy who was admitted to the hospital for two masses, with one below the umbilicus that looked like a hemangiomatous structure and the other in the abdominal skin as a subcutaneous nodule. There was no intraabdominal involvement, and both of the masses were resected at 10 days of life. The one-year follow-up was uneventful. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Turkish J Pediatrics | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | infantile myofibromatosis | en_US |
| dc.subject | abdominal wall | en_US |
| dc.subject | newborn | en_US |
| dc.title | Infantile myofibromatosis in a newborn: a case report | en_US |
| dc.type | article | en_US |
| dc.contributor.department | Kırıkkale Üniversitesi | en_US |
| dc.identifier.volume | 45 | en_US |
| dc.identifier.issue | 1 | en_US |
| dc.identifier.startpage | 59 | en_US |
| dc.identifier.endpage | 63 | en_US |
| dc.relation.journal | Turkish Journal Of Pediatrics | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
