Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/9652
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dc.contributor.authorKareva, Lidijaen_US
dc.contributor.authorStavric, Katarinaen_US
dc.contributor.authorMironska, Kristinaen_US
dc.contributor.authorHasani Arijetaen_US
dc.date.accessioned2020-12-04T13:17:27Z-
dc.date.available2020-12-04T13:17:27Z-
dc.date.issued2019-08-
dc.identifier.issn1312-773X-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/9652-
dc.description.abstractStaphylococcal scalded skin syndrome (SSSS) is skin disease which primarily affects children from newborns up to 5 years of age. When occurring in adults it is accompanied by immunodeficiency. In children, SSSS is usually with good prognosis and resolves with treatment completely, with low mortality, while in adults regarding underline disease mortality is up to 50%. Differential diagnosis includes Steven-Johnson syndrome, Epidermolysis bullosa (EB) and toxic epidermal necrolysis. In this article, we present 8 months old infant with SSSS caused by Staphylococcus aureus strain sensitive to penicillinases. Therapeutic and diagnostic challenges are discussed, together with differential diagnosis and therapy. Successful results are achieved in our case due to the good response to antibiotic and rigorous wound treatment in sterile conditions.en_US
dc.language.isoenen_US
dc.publisherInternational Medical Association Bulgaria (IMAB) / Peytchinski Publishing Ltd.en_US
dc.relation.ispartofJournal of IMABen_US
dc.subjectStaphylococcal scalded skin syndromeen_US
dc.subjectSSSSen_US
dc.titleStaphylococcal Scalded Skin Syndromeen_US
dc.typeArticleen_US
dc.identifier.doi10.5272/jimab.2019253.2655-
dc.identifier.volume25-
dc.identifier.issue3-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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