Lipoblastoma of scalp in a 4-month-old patient: an extremely rare case report and review of the literature
| dc.contributor.author | Demir, Fatih | |
| dc.contributor.author | Ozturk, Sait | |
| dc.contributor.author | Balta, Hilal | |
| dc.contributor.author | Erol, Fatih Serhat | |
| dc.date.accessioned | 2026-08-12T17:19:45Z | |
| dc.date.issued | 2022 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | Lipoblastoma is a rare benign tumor originating from adipose tissue, usually seen in infancy and early childhood. Here, we present a case of scalp lipoblastoma in a 4-month-old that we treated surgically and review the literature. Although lipoblastomas may be seen in various locations during infancy and early childhood, rarely, they can also develop in the scalp. | |
| dc.identifier.doi | 10.1007/s00381-021-05309-2 | |
| dc.identifier.endpage | 1204 | |
| dc.identifier.issn | 0256-7040 | |
| dc.identifier.issn | 1433-0350 | |
| dc.identifier.issue | 6 | |
| dc.identifier.orcid | 0000-0002-7655-0127 | |
| dc.identifier.orcid | 0000-0002-6243-6884 | |
| dc.identifier.pmid | 34368893 | |
| dc.identifier.scopus | 2-s2.0-85112058509 | |
| dc.identifier.scopusquality | Q2 | |
| dc.identifier.startpage | 1201 | |
| dc.identifier.uri | https://doi.org/10.1007/s00381-021-05309-2 | |
| dc.identifier.uri | https://hdl.handle.net/11508/53308 | |
| dc.identifier.volume | 38 | |
| dc.identifier.wos | WOS:000682816100001 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Springer | |
| dc.relation.ispartof | Childs Nervous System | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WoS_20260511 | |
| dc.subject | Lipoblastoma | |
| dc.subject | Scalp | |
| dc.subject | Pediatric | |
| dc.title | Lipoblastoma of scalp in a 4-month-old patient: an extremely rare case report and review of the literature | |
| dc.type | Review Article |







