Langerhans cell histiocytosis: A rare cause of pathological rib fracture
| dc.contributor.author | Yolcu A. | |
| dc.contributor.author | Tulay C.M. | |
| dc.contributor.author | Temiz P. | |
| dc.contributor.author | Aydoğdu İ. | |
| dc.date.accessioned | 2024-07-22T08:06:42Z | |
| dc.date.available | 2024-07-22T08:06:42Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | Langerhans cell histiocytosis, formerly known as histiocytosis X, represents clonal proliferations of the antigen-presenting dendritic cells, which are normally found in many organs. It is a rare disease which tends to affect children and adolescents. In particular, adult-onset type is very rare. Herein, we present a female adult diagnosed with Langerhans cell histiocytosis of the rib without any systemic involvement which was successfully treated with surgery. © 2021. All right reserved by the Turkish Society of Cardiovascular Surgery. | |
| dc.identifier.DOI-ID | 10.5606/tgkdc.dergisi.2021.19685 | |
| dc.identifier.issn | 13015680 | |
| dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/13666 | |
| dc.language.iso | English | |
| dc.publisher | Baycinar Medical Publishing | |
| dc.rights | All Open Access; Bronze Open Access; Green Open Access | |
| dc.title | Langerhans cell histiocytosis: A rare cause of pathological rib fracture | |
| dc.type | Article |