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dc.contributor.authorCetinkaya, Pinar Gur
dc.contributor.authorSekerel, Buelent Enis
dc.contributor.authorSoyer, Ozge Uysal
dc.contributor.authorSahiner, Umit Murat
dc.date.accessioned2019-12-10T10:42:33Z
dc.date.available2019-12-10T10:42:33Z
dc.date.issued2018
dc.identifier.issn1011-7571
dc.identifier.urihttps://doi.org/10.1159/000491586
dc.identifier.urihttp://hdl.handle.net/11655/14241
dc.description.abstractObjective: Acute spontaneous bullous urticaria is an extremely rare entity, and there are few reports with blister formation in acute urticaria patients. Clinical Presentation and Intervention: We present a 2-year-old girl who was admitted for bullous spontaneous acute urticaria; the underlying reason for this was not detected. Nikolsky's sign and Darier's sign were negative. Lesions were not compatible with erythema multiforme. However, biopsy was not allowed to be performed. Because of this, the underlying pathogenesis could not be clarified. The patient recovered by a short course of antihistamine and systemic steroid treatment, and the lesions did not recur during a 2-year follow-up. Conclusion: Short-term systemic steroid in addition to oral antihistamines resulted in prompt recovery in a patient with acute urticaria complicated by bullae. (c) 2018 The Author(s) Published by S. Karger AG, Basel
dc.language.isoen
dc.publisherKarger
dc.relation.isversionof10.1159/000491586
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGeneral & Internal Medicine
dc.titleA Rare Case of Pediatric Bullous Spontaneous Acute Urticaria
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalMedical Principles And Practice
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume27
dc.identifier.issue5
dc.identifier.startpage493
dc.identifier.endpage495
dc.description.indexWoS
dc.description.indexScopus


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