| Literature DB >> 25572600 |
Gianluca Tadini1, Lidia Pezzani2, Stefano Ghirardello3, Paolo Rebulla4, Susanna Esposito2, Fabio Mosca3.
Abstract
Epidermolysis bullosa (EB) is comprised of a group of hereditary mechanobullous disorders that are characterised by extremely fragile skin and mucous membranes. This results in blister formation and non-healing wounds. This case report describes the results of an innovative treatment of two large skin lesions in a newborn with dystrophic recessive EB (DEB) who experienced bacterial superinfections and progressive anaemisation. The lesions were treated with platelet gels derived from allogeneic cord blood (cord blood platelet gel, CBPGs). The skin lesions were clinically evaluated and treated with CBPG weekly until they completely healed. The first and second lesion required CBPG applications for 2 and 4 weeks, respectively. Both lesions were monitored weekly for 6 weeks after the last CBPG application, and no significant relapses were observed during the follow-up period. This case indicates that CBPG is an effective and safe therapeutic option for managing newborns with DEB, particularly as treatment and prevention of fluid loss and superinfection. 2015 BMJ Publishing Group Ltd.Entities:
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Year: 2015 PMID: 25572600 PMCID: PMC4289807 DOI: 10.1136/bcr-2014-207364
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X