Surgical treatment of the patient with Sturge-Weber syndrome - a case report
| Autor: | Adrian Gnatek; Piotr Osica; Anna Janas-Naze |
|---|---|
| Sprache: | Englisch; Spanisch; Polnisch; Russisch; Ukrainisch |
| Veröffentlicht: |
2017 |
| Quelle: | Directory of Open Access Journals: DOAJ Articles |
| Online Zugang: |
http://www.ojs.ukw.edu.pl/index.php/johs/article/view/5035 https://doaj.org/toc/2391-8306 2391-8306 doi:10.5281/zenodo.1049076 https://doaj.org/article/30a8e2bcc97241d296fa0a226ef37b19 https://doi.org/10.5281/zenodo.1049076 https://doaj.org/article/30a8e2bcc97241d296fa0a226ef37b19 |
| Erfassungsnummer: | ftdoajarticles:oai:doaj.org/article:30a8e2bcc97241d296fa0a226ef37b19 |
Zusammenfassung
Vascular malformations associated with genetic syndromes lead to dysfunction of human body organs by blood supply impairment. Disorders in the structure of blood vessels walls result in developing pathological lesions called hemangiomas. The case describes a 16-year-old male patient with Sturge-Weber syndrome (SWS) who was treated surgically due to hemangioma of upper jaw. The patient suffered from typical for Sturge-Weber syndrome congenital disorders of other organs. In these cases surgical treatment requires deep analysis and proper procedure planning in the context of hemostasis.